Published on in Vol 27 (2025)

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/59841, first published .
Trends and Gaps in Digital Precision Hypertension Management: Scoping Review

Trends and Gaps in Digital Precision Hypertension Management: Scoping Review

Trends and Gaps in Digital Precision Hypertension Management: Scoping Review

Review

1School of Nursing, The University of Texas at Austin, Austin, TX, United States

2School of Information, The University of Texas at Austin, Austin, TX, United States

3Department of Electrical and Computer Engineering, The University of Texas at Austin, Austin, TX, United States

Corresponding Author:

Namuun Clifford, MSN

School of Nursing

The University of Texas at Austin

1710 Red River St

Austin, TX, 78701

United States

Phone: 1 (512) 471 7913

Email: namuun.clifford@utexas.edu


Background: Hypertension (HTN) is the leading cause of cardiovascular disease morbidity and mortality worldwide. Despite effective treatments, most people with HTN do not have their blood pressure under control. Precision health strategies emphasizing predictive, preventive, and personalized care through digital tools offer notable opportunities to optimize the management of HTN.

Objective: This scoping review aimed to fill a research gap in understanding the current state of precision health research using digital tools for the management of HTN in adults.

Methods: This study used a scoping review framework to systematically search for articles in 5 databases published between 2013 and 2023. The included articles were thematically analyzed based on their precision health focus: personalized interventions, prediction models, and phenotyping. Data were extracted and summarized for study and sample characteristics, precision health focus, digital health technology, disciplines involved, and characteristics of personalized interventions.

Results: After screening 883 articles, 46 were included; most studies had a precision health focus on personalized digital interventions (34/46, 74%), followed by prediction models (8/46, 17%) and phenotyping (4/46, 9%). Most studies (38/46, 82%) were conducted in or used data from North America or Europe, and 63% (29/46) of the studies came exclusively from the medical and health sciences, with 33% (15/46) of studies involving 2 or more disciplines. The most commonly used digital technologies were mobile phones (33/46, 72%), blood pressure monitors (18/46, 39%), and machine learning algorithms (11/46, 24%). In total, 45% (21/46) of the studies either did not report race or ethnicity data (14/46, 30%) or partially reported this information (7/46, 15%). For personalized intervention studies, nearly half (14/30, 47%) used 2 or less types of data for personalization, with only 7% (2/30) of the studies using social determinants of health data and no studies using physical environment or digital literacy data. Personalization characteristics of studies varied, with 43% (13/30) of studies using fully automated personalization approaches, 33% (10/30) using human-driven personalization, and 23% (7/30) using a hybrid approach.

Conclusions: This scoping review provides a comprehensive mapping of the literature on the current trends and gaps in digital precision health research for the management of HTN in adults. Personalized digital interventions were the primary focus of most studies; however, the review highlighted the need for more precise definitions of personalization and the integration of more diverse data sources to improve the tailoring of interventions and promotion of health equity. In addition, there were significant gaps in the reporting of race and ethnicity data of participants, underuse of wearable devices for passive data collection, and the need for greater interdisciplinary collaboration to advance precision health research in digital HTN management.

Trial Registration: OSF Registries osf.io/yuzf8; https://osf.io/yuzf8

J Med Internet Res 2025;27:e59841

doi:10.2196/59841

Keywords



Background

Hypertension (HTN) is the leading preventable cause of cardiovascular disease and premature mortality worldwide, affecting an estimated 1.28 billion adults [1]. It surpasses smoking, diabetes, and obesity as the most significant modifiable risk factor, contributing to 54% of stroke and 47% of ischemic heart disease cases [2,3]. Despite mounting evidence that antihypertensive treatment can reduce morbidity and mortality, HTN remains underdiagnosed and undertreated [4,5]. Globally, nearly half of adults with HTN are unaware that they have the condition, and only 21% have their blood pressure (BP) under recommended levels [1]. Significant disparities exist in HTN prevalence and management. While 82% of individuals with HTN live in low- and middle-income countries, only 7.7% achieve BP control, compared to 28.4% in high-income countries [4,6]. These disparities have been linked to various social and environmental determinants that disproportionately affect individuals from racial and ethnic minority groups [7]. Given the considerable global health burden and inequities stemming from suboptimal HTN management, there is an urgent demand for innovative and scalable solutions for effective HTN prevention and control.

Challenges in HTN Management

Despite the availability of effective treatments, only 21% of adults with HTN worldwide have their BP under control [6]. Longitudinal analyses have shown that up to 50% of patients stop taking their prescribed medications within 1 year; this is attributed to factors such as sociodemographics, medication side effects, lack of knowledge, comorbidities, lack of access to care, and patient-clinician relationship [8,9]. Current HTN treatment approaches are based on evidence from randomized controlled trials (RCTs) that reflect the mean results for the average patient [10]. This “one-size-fits-all” approach fails to consider the wide variation in an individual’s genetic, biological, behavioral, sociodemographic, and environmental factors that profoundly influence HTN treatment adherence and outcomes. This lack of personalization contributes to suboptimal treatment adherence and poor overall HTN control [9]. Effective management strategies must incorporate more nuanced approaches that adapt to the unique characteristics and contexts of individuals within diverse populations.

Digital Precision Health for HTN Management

The emergence of precision health as a paradigm to empower individuals, predict and prevent disease before it starts, and personalize care addresses these challenges and presents a promising road map for transforming HTN management [11]. Expanding on precision medicine’s focus on personalized medical care, precision health goes beyond treatment, emphasizing health promotion and disease prevention for a more proactive approach to addressing population health [11-14]. Interventions in precision health are customized to the individual’s unique variations in genetic, biological, behavioral, sociocultural, and environmental determinants to improve health outcomes [14-16]. While personalized care has always been a goal in clinical practice, it is only with recent technological advancements in artificial intelligence, data analytics, and digital tools that the depth of personalization and predictive capabilities in disease risk or treatment response are becoming truly attainable [16]. Digital health technologies, including mobile apps, wearable devices, and remote monitoring, enable the harnessing of data to tailor interventions, predict disease risk, and engage patients more effectively in their care [11]. These tools present an opportunity to overcome traditional care barriers, facilitating more accessible, accurate, timely, and personalized HTN prevention and management strategies.

Objectives

Although existing research has examined the effectiveness of digital interventions in improving health outcomes for HTN, there is a notable lack of prior reviews that integrate these findings in the context of precision health [12-15]. The primary objective of this scoping review is to synthesize the existing studies pertaining to precision health using various digital health technologies for the management of HTN in adults. Specifically, we aimed to address the following questions:

  1. Which aspects of precision health are addressed (ie, prediction models, personalization, and phenotyping), and what are the characteristics of these studies?
  2. Which digital health tools are being used in precision HTN management?
  3. What are the characteristics of participants in precision health studies for HTN management?
  4. For personalized interventions, what types of data are used for personalization, and what are the characteristics of personalization?

By mapping out the current state of digital precision health for HTN management, we seek to provide a foundation for future research, policy, and the development of effective and equitable interventions to improve the prevention, diagnosis, and management of HTN on a global scale.


Design

This scoping literature review was conducted following the framework for scoping reviews developed by Arksey and O’Malley [17]. This framework consists of five stages: (1) identifying the research question; (2) identifying relevant studies; (3) study selection; (4) charting the data; and (5) collating, summarizing, and reporting the results. Thematic analysis of findings were conducted based on the 3 categories of studies included in the review: personalized interventions, phenotyping, and prediction models. The review used the PRISMA-ScR (Preferred Reporting Items for Systematic Reviews and Meta-Analyses extension for Scoping Reviews) reporting guidelines to increase methodological transparency (Multimedia Appendix 1) [17]. The review protocol was registered with the OSF Registries (osf.io/yuzf8).

Search Methods

In July 2023, assisted by a research librarian, we conducted comprehensive searches across 5 databases: PubMed, CINAHL, Web of Science, Embase, and Inspec. We filtered the search for peer-reviewed articles published between 2013 and 2023 in the English language. This 10-year time frame was chosen to capture the most recent and relevant advancements in digital health technologies and their application in HTN management. Search terms included “precision health” (eg, precision medicine OR personalized OR tailored OR individualized) AND “digital health” (telemedicine OR telehealth OR mobile apps OR wearable electronic devices OR electronic health) AND “hypertension” (high blood pressure OR elevated blood pressure). Medical subject headings terms were adapted across databases. The full search strategy is provided in Multimedia Appendix 2.

Final search results were transferred to an EndNote (version 20) database, and duplicates were removed. The remaining articles were imported into Covidence, a web-based software platform designed for conducting literature reviews. Blinded screening of title, abstract, and full texts was conducted by 3 authors (NC, RT, and AA), with each study independently reviewed by 2 of these authors. Any conflicts in opinion were reconciled through discussion or, if needed, by involving a third reviewer (HR).

Eligibility Criteria

This scoping review sought to comprehensively map key concepts within the identified research area by including all types of research designs of original, peer-reviewed research papers. In addition, studies were included if they (1) sampled adults aged ≥18 years, (2) contained a diagnosis of HTN, (3) had a precision health focus, and (4) used a digital health technology. If studies included participants with >1 diagnosis (ie, HTN and diabetes mellitus), and HTN management was a primary focus of the intervention, they were included. To identify studies with a focus on precision health, if the term precision health or its synonyms (ie, personalized, tailored, individualized, predictive, and phenotype) were in the title, abstract, or main text, they were included. For the detailed eligibility criteria, refer to Textbox 1.

Textbox 1. Eligibility criteria for scoping review.

Inclusion criteria

  • Study type: original peer-reviewed research paper
  • Period: studies published between January 1, 2013, and July 20, 2023
  • Language: English
  • Population: adults aged ≥18 years with a diagnosis of hypertension
  • Had a precision health focus (ie, predictive, personalized, or phenotyping)
  • Used a digital health technology (eg, mobile phones, telemedicine, wearable devices, or electronic health records)

Exclusion criteria

  • Study types: case studies, editorials, opinion pieces, gray literature, dissertations, literature reviews, and trial protocols
  • Period: studies published before January 1, 2013, or after July 20, 2023
  • Language: any language other than English
  • Population: pediatric or pregnant patients
  • Pulmonary artery hypertension diagnosis
  • Interventions targeting health care providers

Studies were excluded if they involved pediatric or pregnant participants, had a diagnosis of pulmonary artery HTN, or reported interventions targeting health care providers. Pregnant individuals were excluded due to the unique physiological and treatment differences in managing HTN during pregnancy, such as gestational HTN or preeclampsia, which is considerably outside the scope of this review. Furthermore, we excluded case studies, editorials, opinion pieces, gray literature, dissertations, literature reviews, and trial protocols, as these are secondary or nonempirical sources lacking original research data essential for our analysis.

Data Extraction

We developed 3 separate data extraction templates, each containing fields for all identified key data elements. The first template was used to extract data on study characteristics, including study location, design, sample characteristics, precision health focus, digital health technology used, and disciplines involved. The other templates were used to extract data on personalization characteristics and types of data used for personalization of tailored intervention studies. For each included study, the first author (NC) and 1 of the 3 coauthors (RT, AA, and HY) independently extracted data using the standardized templates. This dual-reviewer approach was used to minimize errors and biases in the data extraction process. Any discrepancies between reviewers in the data extraction were resolved through discussion, with a third author available for consultation if consensus could not be reached.

Data Synthesis

Included studies were categorized based on their precision health focus: personalization, phenotyping, and prediction models. We conducted thematic analysis to identify recurring themes and patterns across the studies, with themes derived both deductively from the research objectives and inductively from the study findings [18]. Studies were cross-compared to highlight differences and similarities in methodologies, designs, and outcomes. Synthesizing the extracted data allowed us to identify gaps in the current research landscape, generating recommendations for future research directions which we discuss in this study.


Search Results

The search yielded 883 studies after the removal of duplicates; after title and abstract screening, we identified 104 (12%) studies for full-text review. Of the 104 studies, a final sample of 46 (44%) studies met the inclusion criteria for this review (Figure 1). In alignment with the scoping review methodology, we did not conduct a quality appraisal of the included studies, as our goal was to rapidly identify and synthesize the existing evidence of digital precision health research for HTN management [16].

Figure 1. PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) flow diagram of study selection.

Summary of the Included Studies

Table 1 provides an overview of the included studies. Most studies were conducted in or used data from North America, predominantly from the United States (30/46, 65%), with 1 (2%) study conducted in Canada. Of the 46 studies, 7 (15%) were conducted in or used data from Europe, followed by 6 (13%) from Asia and 1 (2%) from Brazil in South America. Of the 46 studies, 1 (2%) study on genome sequencing used data from both the United States and the United Kingdom [19]. Nearly half of the studies (21/46, 46%) were RCTs, of which 8 (17%) were pilot or feasibility RCTs. There was a diverse mix of studies comprising qualitative, mixed methods, and analytical observational (eg, cohort and cross-sectional) designs in addition to the RCTs.

In terms of precision health focus, most studies (34/46, 74%) focused on personalization, 8 (17%) focused on prediction models, and 4 (9%) focused on phenotyping (Figure 2). Disciplines involved were predominantly within the health sciences (29/46, 63%), with over a third of studies (15/46, 33%) featuring interdisciplinary teams comprising ≥2 disciplines (eg, medical and health sciences, informatics, and computer and electrical engineering). All included studies (46/46, 100%) sampled populations with HTN, with additional diagnoses of diabetes mellitus (16/46, 35%), hyperlipidemia (7/46, 15%), and classifications of overweight or obesity (3/46, 7%).

Table 1. Summary of the included studies (N=46).
Characteristics and categoriesStudies, n (%)
Study location

North America (the United States and Canada)31 (67)

Europe (Spain, Ireland, the United Kingdom, and Sweden)7 (15)

Asia (South Korea, Japan, Lebanon, Hong Kong, and China)6 (13)

South America (Brazil)1 (2)

Multiple locations (the United States and the United Kingdom)1 (2)
Study design

RCTsa (including pilot or feasibility)21 (46)

Analytical observational16 (35)

Qualitative5 (11)

Mixed methods3 (7)

Proof of concept1 (2)
Precision health focus

Personalization34 (74)

Prediction models8 (17)

Phenotyping4 (9)
Disciplines involved

Health sciences29 (63)

Computer and electrical engineering1 (2)

Informatics and communication sciences1 (2)

Interdisciplinary team (≥2 disciplines)15 (33)
Clinical conditions of the sample

Hypertension46 (100)

Diabetes mellitus16 (35)

Hyperlipidemia7 (15)

Overweight or obesity3 (7)

Others (bipolar disorder, kidney transplant, and stroke)3 (7)

aRCT: randomized controlled trial.

Figure 2. Studies published by year and precision health focus.

Study Characteristics

Study characteristics are presented in Multimedia Appendix 3, and a summary of the sample characteristics is presented in Table 2. Sample sizes in the studies ranged from 7 to 764,135. Nearly half (21/46, 46%) of the studies had a sample size <100, followed by 11 (24%) studies with a sample size between 100 and 499 and 6 (13%) with a sample size >10,000. Most studies (33/46, 72%) included participants with a mean age between 50 and 69 years. The range of female participants across all studies was 1.4% to 100%, with a median of 51% (IQR 40-62). Of the 46 studies, 14 (30%) did not report the race or ethnicity of participants.

Table 2. Summary of sample characteristics from the included studies (N=46).
Characteristic and categoryStudies
Sample size, n (%)

<9921 (46)

100-49911 (23.9)

500-9993 (6.5)

1000-99995 (10.87)

>10,0006 (13.04)
Mean agea (y), n (%)

18-290 (0)

30-390 (0)

40-495 (11)

50-5918 (39)

60-6915 (33)

>701 (2)

Not reported2 (4)
Race and ethnicityb

African American or Black, n (median %c, IQR)21 (39.7, 11.8-53.8)

American Indian or Alaska Native, n (median %c, IQR)0 (0, 0)

Asian, n (median %c, IQR)7 (1.0, 0-2.8)

Hawaiian or Pacific Islander, n (median %c, IQR)0 (0, 0)

Hispanic or Latinx, n (median %c, IQR)17 (5.2, 2.1-14.3)

Non-Hispanic White, n (median %c, IQR)23 (50.9, 23.0-74.6)

Other, n (median %c, IQR)12 (2.8, 0-4.7)

Not reported, n14

Partially reported, n7
Genderd

Female, n (median %, IQR)39 (51, 40-62)

Not reported, n2

aMean age: Studies that cited another study or database for participant age (n=6) were excluded from the breakdown above.

bRace and ethnicity: Studies that cited another study or database for race and ethnicity (n=4) were excluded from the breakdown above.

cMedian %: median percentage across the reported studies.

dGender: Studies that cited another study or database for gender (n=5) were excluded from the breakdown above.

Digital Personalization for HTN Management

Overview

Of the 46 studies, 34 (74%) had a precision health focus of personalization in HTN management (Table 3). These studies tested or assessed digital interventions that were tailored to the individual or group characteristics of its users. Most studies (30/34, 88%) tested a personalized digital intervention and were primarily quantitative in design (eg, cohort, RCTs and mixed methods). Of the 34 personalization studies, 4 (13%) were qualitative and described participants’ views on technology-based interventions. Sample sizes ranged from 11 to 10,803, and the most commonly reported primary outcomes included BP (21/34, 62%), medication adherence (4/34, 12%), participants’ views or feedback (4/34, 12%), and feasibility and satisfaction of the intervention (3/34, 9%). Digital technologies used most often in these studies included mobile phones (30/34, 88%), followed by BP monitors (17/34, 50%), wearable devices (4/34, 12%), electronic medication trays or pillboxes (3/34, 9%), web platforms (2/34, 6%), and tablets (2/34, 6%).

Table 3. Summary of studies on digital personalization for hypertension (n=34).
First authorStudy designSample sizeDigital technologyPrimary outcomes
Beran et al [20]Mixed methods450Mobile phone and BPa monitorBP
Blood et al [21]Cohort10,803Mobile phone and BP monitorBP
Bosworth et al [22]RCTb428Mobile phone and BP monitorCVDc risk score
Brewer et al [23]Mixed methods16Mobile phoneBP
Chandler et al [24]RCT56Mobile phone, BP monitor, and electronic medication trays and pill boxesBP
Choudhry et al [25]RCT4078Mobile phoneMedication adherence
David et al [26]Secondary analysis of RCT231Mobile phone and BP monitorBP
Davidson et al [27]RCT38Mobile phone, BP monitor, electronic medication trayBP
Glynn et al [28]Qualitative50Views on technologyViews on technology
Guthrie et al [29]Cohort172Mobile phone and BP monitorBP
Hellem et al [30]Qualitative86Mobile phoneFeedback on the design of the mobile app intervention
Jeong et al [31]Pilot RCT35Mobile phone and BP monitorHealth behavior and BP
Kario et al [32]RCT390Mobile phone and BP monitorBP
Kassavou et al [33]RCT135Mobile phoneMedication adherence
Klein et al [34]Cohort38Mobile phoneMedication adherence
Leitner et al [35]RCT38Wearable device, mobile phone, and BP monitorBP
Lewinski et al [36]Pilot RCT118Mobile phoneBP
Lv et al [37]Pre-post149Mobile phone, BP monitor web-based system, and wearable deviceBP
McBride et al [38]Qualitative11Mobile phone and BP monitorFeedback using app
McGillicuddy et al [39]Pilot RCT20Mobile phone, BP monitor, electronic medication trayBP and medication adherence
Naqvi et al [40]Pilot RCT50Electronic tablet and BP monitorBP
Payne Riches et al [41]Pilot RCT47Mobile phoneFollow-up, fidelity, and app use
Petrella et al [42]RCT149Mobile phone, BP monitor, and wearable deviceBP
Rodriguez et al [43]RCT544Mobile phoneBP
Rodriguez et al [44]RCT533Mobile phoneStage of change and DASHd score
Saleh et al [45]Mixed methods606Mobile phonePatient satisfaction
Schoenthaler et al [46]Pilot RCT42Electronic tabletIntervention acceptance and BP
Shea et al [47]Pilot RCT140Mobile phoneBP
Steinberg et al [48]Pilot RCT140Mobile phoneDiet tracking and DASH score
Thiboutot et al [49]RCT500WebsiteBP
Van Emmenis et al [50]Qualitative20Mobile phoneViews on the mobile app intervention
Wang et al [51]Pilot RCT49Mobile phone and BP monitorFeasibility of app use
Willis et al [52]Cohort7752Mobile phone and BP monitorBP
Zhang et al [53]RCT192Wearable device and mobile phoneBP

aBP: blood pressure.

bRCT: randomized controlled trial.

cCVD: cardiovascular disease.

dDASH: dietary approaches to stop hypertension.

Of the 34 studies, 4 (12%) qualitative studies highlighted participants’ perceived importance of personalization in digital interventions. Participants emphasized the need for digital interventions to be customizable, allowing for tailoring based on their preferences, such as personalizing functions for SMS text messages, the inclusion of all medications in the app, and the ability to adjust reminder settings [28,50]. A study on the design of a mobile app intervention found distinct differences in preferences between participants from a federally qualified health center and a university cardiovascular clinic; the former group placed greater value on social support themes and addressing health-related social needs [30]. McBride et al [38] found that participants using a mobile app for home BP monitoring felt the app’s visual feedback and medication reminders improved their understanding of their condition as well as their sense of control and responsibility, resulting in improved self-management practices.

Personalization Characteristics of the Digital Interventions
Modalities and Approaches

For the 30 studies that tested a personalized digital intervention (Table 4), the modality of intervention delivery occurred exclusively through mobile apps for half of the studies (n=16, 53%), phone calls only (n=5, 17%), SMS text messages only (n=2, 7%), and web- or tablet-based only (n=2, 7%). Of the 30 studies, 6 (20%) used ≥2 modalities (ie, phone calls, texts, emails, and mobile apps) for intervention delivery. Of the 30 studies, 19 (63%) used personnel (eg, case managers, patient navigators, and clinicians) for some aspect of the intervention design and delivery, while 11 (37%) studies relied solely on digital technology for intervention delivery.

Table 4. Personalization characteristics of the digital interventions (n=30).
First authorPersonnelHuman vs automated tailoringPersonalized elements of interventionStudy findings
Beran et al [20]PharmacistsHybrid
  • Tailored education
  • Individualized medication management
CSa
Blood et al [21]Pharmacists, patient navigators, and NPsb and MDscHybrid
  • Tailored education
  • Individualized medication management
SSd
Bosworth et al [22]PharmacistsHuman
  • Tailored education
  • Individualized medication management
NSe
Brewer et al [23]Community health workers and cliniciansHybrid
  • BPf and medication tracking on an app
  • Culturally tailored education
  • Assessment of SDoHg needs and referrals for services (housing and utilities)
CS
Chandler et al [24]hAutomated
  • Reminders, feedback, and motivational messages based on treatment adherence, and values, beliefs, or goals
SS
Choudhry et al [25]PharmacistsHybrid
  • Tailored education
  • Assessment of SDoH needs and referrals for social work and affordable prescription options
SS
David et al [26]Automated
  • Tailored education
  • Personalized feedback based on BP, goals, and treatment adherence
SS
Davidson et al [27]Automated
  • Culturally tailored SMS text messages based on treatment adherence and values, beliefs, or goals
SS
Guthrie et al [29]Multidisciplinary teamHybrid
  • AIi-assisted tailored feedback and education on self-management and treatment adherence
SS
Jeong et al [31]NursesHuman
  • Tailored education addressing self-management behaviors and treatment adherence
CS
Kario et al [32]Health professionals and chat-bot based virtual nursesHybrid
  • Personalized lifestyle program based on age, sex, lifestyle, social background, and behavior patterns
SS
Kassavou et al [33]CliniciansAutomated
  • Tailored messages on improving medication adherence based on patient beliefs, attitudes, self-efficacy, and emotional state
  • Medication refill reminders sent via SMS text messages
SS
Klein et al [34]Automated
  • Tailored SMS text messages to improve medication adherence comprising educational and motivational content
CS
Leitner et al [35]Automated
  • AI-driven personalized lifestyle recommendations based on clinical, behavior, and psychological data
CS
Lewinski et al [36]Case managerHuman
  • Tailored education on self-management behaviors and treatment adherence
NS
Lv et al [37]Case manager, dietitian, and pharmacistHuman
  • Individualized BP management plan
  • Tailored feedback on BP, medicines, weight, steps, and diet
SS
McGillicuddy et al [39]Automated
  • Tailored reminders, feedback, and summary reports including positive reinforcement and suggestions for improvement
  • Tailored to medication dosing schedule and BP goals
SS
Naqvi et al [40]NPs or MDs and pharmacistsHuman
  • Individualized consultations regarding symptoms and medication changes
  • BP infographics tailored to BP at discharge, available in English and Spanish
SS
Payne Riches et al [41]CliniciansHybrid
  • Individualized goal setting and feedback on participants’ food choices to help them identify lower-salt options
CS
Petrella et al [42]Exercise specialistsHuman
  • Tailored exercise program prescribed by an exercise specialist based on fitness level
NS
Rodriguez et al [43]CounselorsHuman
  • Tailored counseling based on the stage of change for adherence to exercise, diet, and medication adherence
  • Individualized assessment of barriers to behavior changes and solutions
SS
Rodriguez et al [44]CounselorsHuman
  • Tailored counseling based on the stage of change for DASHj diet, exercise, and medication adherence
SS
Saleh et al [45]Automated
  • Personalized reminders for appointments, laboratory tests, and examinations
  • Content tailored to language and health literacy
SS
Schoenthaler et al [46]Research assistantAutomated
  • Personalized list of adherence intervention strategies based on unique barriers to treatment adherence
SS
Shea et al [47]Automated
  • Tailored educational texts based on participants’ priority topics and most recent BP reading
CS
Steinberg et al [48]Automated
  • Tailored messages based on adherence to the DASH diet
  • Content was tailored for women and provided behavioral tips to reinforce dietary change and provide social support
NS
Thiboutot et al [49]Automated
  • Customized feedback and recommendations on questions to discuss with their health care providers
NS
Wang et al [51]Automated
  • Individual monitoring of treatment response and tailored recommendations for follow-up based on BP levels
CS
Willis et al [52]MDsHuman
  • Individualized remote treatment based on BP levels
SS
Zhang et al [53]Health facilitatorsHuman
  • Tailored feedback on self-management behaviors
CS

aCS: clinically significant but not statistically significant.

bNP: nurse practitioner.

cMD: medical doctor.

dSS: statistically significant.

eNS: no statistical or clinical significance.

fBP: blood pressure.

gSDoH: social determinants of health.

hNot applicable.

iAI: artificial intelligence.

jDASH: dietary approaches to stop hypertension.

Personalization strategies varied, with 13 (43%) of the 30 studies using a fully automated personalization approach without the need for human involvement. For example, interventions used automated SMS text messages to improve treatment adherence and provide feedback to participants [24,26,34] or used an artificial intelligence–driven system to generate weekly tailored lifestyle recommendations [35]. Of the 30 studies, 10 (33%) used human-driven personalization, in which study personnel were the primary avenues for personalization of the intervention. For example, nurses and case managers offered patients personalized education on self-management behaviors and treatment adherence [31,36], and pharmacists and physicians provided individualized medication adjustments based on treatment response [22,52]. Of the 30 studies, 7 (23%) used a hybrid approach (ie, both the technology and human study personnel contributed to the personalization of the intervention).

Most personalized intervention studies (25/30, 83%) had either statistically significant positive outcomes (16/30, 53%) or improved or clinically meaningful outcomes, although not statistically significant (9/30, 30%). The studies with nonsignificant, yet positive findings tended to be pilot studies or had small sample sizes (ie, <40 participants). Among the 25 studies with significant positive outcomes, 16 (64%) involved personnel in intervention delivery, with involvement levels varying from comprehensive multidisciplinary teams (pharmacists, nurse practitioners, physicians, and patient navigators) offering patient education, medication management, and monitoring [21], to minimal, such as research assistants giving participants tablet use instructions [46]. In addition, 48% (12/25) of these studies used an automated tailoring approach, followed by 28% (7/25) of the studies using human-led tailoring and 24% (6/25) using a combination of both human-led and automated tailoring.

Personalized Elements of the Interventions

Personalized interventions included tailored education on self-management (ie, medication adherence, diet, and exercise), along with motivational messages and feedback aligned with each participant’s adherence, values, beliefs, and goals. For instance, a culturally adapted mobile health intervention sent the following message to a Hispanic man hoping to find a wife and start a family: “Get back on track taking your meds for building that stronger, healthier body for when you meet that special woman” [24]. Studies also provided personalized reminders for medications, appointments, laboratory tests, and individualized medication management based on treatment adherence and BP levels. Of the 30 studies, only 2 (7%) provided assessment and referrals for social determinants of health needs (ie, housing, utilities, and affordable prescription options) [23,25].

Data Used for Personalization

Tailored intervention studies used a range of data types for personalization of the intervention (Table 5). From 8 categories of data available for personalization (eg, demographic, clinical, and behavioral), just over half the studies (16/30, 53%) used ≥3 types of data, with 14 (47%) studies using ≤2 data types. Of the 30 studies, 6 (20%) used 5 categories of data for personalization, with no studies using >5 data types. The 3 most common types of data used for personalization were behavioral (28/30, 93%), clinical (24/30, 80%), and psychological (17/30, 57%). Behavioral data were typically used to monitor patients’ adherence to key behaviors relevant to HTN management, such as taking medication, physical activity, and diet. Collecting real-time information on participants’ health behaviors allowed for individualized feedback in many studies. For example, in the study by Steinberg et al [48], participants reported their food intake and could receive texts with feedback and guidance, such as “You did best with reducing saturated fat and boosting your fiber intake and seemed to struggle with getting enough potassium and magnesium...to get more magnesium, try dried fruit as a snack!” Similarly, clinical data such as BP or medication-related information were used to offer feedback tailored to participant’s clinical metrics. For instance, Wang et al [51] developed a telehealth system that used decision rules to adjust care based on BP levels; if BP was optimal and participants were adherent to medications without side effects, follow-up appointments could be deferred and medication refills could be automatically prescribed. Psychological data included information on participants’ attitudes, beliefs, values, and goals. For example, a few studies assessed participants’ “stage of change” [43,44] and readiness to modify behaviors [25], while others took into account their values, attitudes, and beliefs [24,27,34] or their perceived barriers to self-management [25,36,43,46].

Table 5. Data types used for personalization in digital interventions (n=30).
StudyDemographic (n=4)Socioeconomic (n=6)Clinical (n=24)Behavioral (n=28)Psychologic (n=17)Health literacy (n=6)Physical environmentCultural (n=4)
Beran et al [20]

  
 
Blood et al [21]  
  
 
Bosworth et al [22]  ✓  
Brewer et al [23] ✓   ✓ 
Chandler et al [24]  
  ✓
Choudhry et al [25]  ✓   
David et al [26]      
Davidson et al [27]  ✓   ✓
Guthrie et al [29]     
Jeong et al [31] ✓    
Kario et al [32]✓ ✓    
Kassavou et al [33]      
Klein et al [34]      
Leitner et al [35]     
Lewinski et al [36]  ✓ ✓  
Lv et al [37]     
McGillicuddy et al [39]     
Naqvi et al [40]     
Payne Riches et al [41]    ✓   
Petrella et al [42]   ✓    
Rodriguez et al [43]  ✓ ✓    
Rodriguez et al [44]   ✓    
Saleh et al [45]   ✓    
Schoenthaler et al [46]  ✓ ✓   ✓ 
Shea et al [47]   ✓    
Steinberg et al [48]✓       
Thiboutot et al [49]  ✓ 
    
Wang et al [51]  ✓     
Willis et al [52]   ✓    
Zhang et al [53]  ✓     

The other types of data used for personalization were all used by less than one-third of the studies: health literacy (6/30, 20%), social and economic (6/30, 20%), demographics (4/30, 13%), and cultural (4/30, 13%). No studies obtained physical environment data for personalization of the intervention. For health literacy, the prevailing strategy involved designing interventions for a low-literacy population as a whole, rather than tailoring it at the individual participant level, and none of the studies tailored interventions to the level of digital literacy [36,45,54]. Similarly, studies implementing cultural tailoring primarily focused on specific populations as opposed to tailoring at the individual level. For example, Brewer et al [23] and Schoenthaler et al [46] both conducted studies with only Black participants and offered culturally tailored content geared for this population, such as education on the impact of racism and discrimination on BP. However, not all studies applied cultural tailoring broadly. Davidson et al [27] assessed cultural values and beliefs at an individual level, sending customized SMS text messages based on these insights.

Digital Phenotyping

There were 4 studies with a precision health focus on phenotyping [19,55-57] using a range of demographic, behavioral, clinical, and genetic data to apply phenotyping in diverse ways to enhance understanding and management of HTN (Table 6). Sample sizes ranged from 13 for a qualitative study [57] to 764,135 in a whole-genome sequencing analysis [19]. Digital tools used included mobile phones (2/4, 50%), web platform (1/4, 25%), electronic health record (EHR; 1/4, 25%), machine learning (ML) algorithms (1/4, 25%), BP monitor (1/4, 25%), and genomic databases (1/4, 25%).

Table 6. Summary of the studies on digital phenotyping for HTNa.
First authorStudy designSample sizeDigital technologyDescription of the study
Bakre et al [55]Secondary data analysis11,934Mobile phone and web platformThe study analyzed demographic, dietary, and clinical data of participants with stage 2 HTN who used a digital nutrition platform to identify characteristics associated with greater reductions in BPb.
Chen et al [56]Secondary data analysis2521EHRc and MLd algorithmThe study developed an ML framework to identify predictive features and cluster patients with HTN into 4 clinically meaningful groups of disease severity.
Hellem et al [57]Qualitative13Mobile phone and BP monitorThe study examined participants’ determinants of engagement from a digital intervention through interviews, phenotyping participants into high engagers, low engagers, and early enders.
Kelly et al [19]Genome sequencing764,135Genomic databasesThis is the first study to identify a promising but unconfirmed intergenic rare variant associated with BP. This variant lowered SBPe by an average of 33 mm Hg in carriers compared with noncarriers, and all participants were of Asian ancestry.

aHTN: hypertension.

bBP: blood pressure.

cEHR: electronic health record.

dML: machine learning.

eSBP: systolic blood pressure.

Of the 4 studies, 2 (50%) used secondary data analysis to apply phenotyping. Bakre et al [55] applied phenotyping by analyzing demographic, dietary, and clinical data of participants with stage 2 HTN who used a digital nutrition platform, identifying characteristics associated with a decrease in BP. They found that participants who achieved greater BP reductions had higher reductions in weight and dietary improvements, suggesting the effectiveness of digital nutrition guidance on management of HTN [55]. Chen et al [56] used EHR data to develop an ML framework to phenotype patients with HTN into 4 clinically meaningful groups, aiming to improve personalization of care and resource allocation. They used demographic and clinical data for cluster analysis, identifying 2 groups with mild disease and 2 with more severe disease profiles.

The qualitative study by Hellem et al [57] explored participants’ determinants of engagement from a SMS text messaging intervention to reduce BP among patients with HTN. Through interviews with participants purposely sampled from 3 engagement categories—high engagers, low engagers, and early enders—this study phenotyped individuals based on a mix of social, psychological, and environmental factors, including digital literacy and access. They found that high engagers had a better understanding of the intervention, the least number of social needs, and the greatest social support. In contrast, early enders and low engagers expressed greater amounts of social needs and less social support [57]. Finally, the study by Kelly et al [19] phenotyped participants at a genetic level, offering a direct link between genotype and phenotypic expression of BP, presenting a road map for targeted genetic interventions for personalized management of HTN.

Digital Prediction Tools

There were 8 studies with a precision health focus on prediction models (Table 7). These studies collectively explored advanced ML techniques for personalized risk prediction for HTN management. Study designs were primarily ML model development (7/8, 88%), with 1 (13%) proof-of-concept study [58] and 1 (13%) hybrid design comprising both ML model development and RCT [59]. Sample sizes varied from 7 for the proof-of-concept study [58] to 245,499 for the study using EHR data [60]. Digital technologies used for these studies included the following: ML algorithms (8/8, 100%), EHR (5/8, 63%), wearable devices (4/8, 50%), mobile phone and web platform (1/8, 13%), and BP monitor (1/8, 13%). Various ML models were used for each of these studies, with half of the studies using random forest models (4/8, 50%), with others including online recurrent extreme learning machine and long short-term memory.

Table 7. Summary of the studies on prediction models for HTNa (n=8).
First authorStudy designSample sizeDigital technologyStudy descriptionMLb models
Abrar et al [61]ML model development35ML algorithmsDevelopment of a personalized BPc prediction model tailored to individual physiology and lifestyle factorsOR-ELMd
Bernal et al [58]Proof of concept7ML algorithms, wearable device, mobile phone, and web platformDevelopment of an intelligent web-based ecosystem that integrates clinical, behavioral, and environmental data to predict adverse high BP eventsBayesian ridge, support vector regression, and random forest
Bertsimas et al [62]ML model development19,926ML algorithms and EHReDevelopment of ensemble ML models for personalized predictions and treatment recommendations, with significant improvements in HTN through optimal treatment prescriptions based on individual patient dataClassification models (eg, multivariate logistic regression and random forests) and regression models (eg, support vector regression and optimal regression trees)
Cano et al [63]ML model development86ML algorithms, wearable device, and EHRDevelopment of a system for improved discrimination between healthy individuals, individuals with prehypertension, and individuals with HTN using PPGf and ECGg signals, focusing on improving the accuracy of HTN detectionA total of 37 different classification models were used: logistic regression, support vector machines, and nearest neighbors, with the Coarse Tree model achieving the highest discrimination
Chiang et al [59]RCTh and ML model development25ML algorithms, wearable device, and BP monitorDevelopment of a personalized BP model for each individual using clinical and behavioral data, identifying the most important lifestyle factors impacting BP trend, and providing precise recommendations for HTN managementRandom forest with Shapley value–based feature selection model outperformed other models in prediction accuracy
Hu et al [64]ML model development42,792ML algorithms, wearable device, and EHRDevelopment of an ML model for personalized antihypertensive medication classes for patients with HTN using a robust algorithm that accommodates outliers in EHR dataThe distributionally linear regression–informed k-nearest neighbors model resulted in a 14.22 mm Hg reduction in SBPi on average
Jimeng et al [65]ML model development1294ML algorithms and EHRDevelopment of ML model to predict transition points in HTN control status, aiming to inform personalized management strategiesLogistic regression, naïve Bayes, and random forests
Ye et al [60]ML model development245,499ML algorithms and EHRDevelopment of deep learning models to predict individualized HTN treatment pathways based on EHR dataLSTMj and bidirectional LSTM

aHTN: hypertension.

bML: machine learning.

cBP: blood pressure.

dOR-ELM: online recurrent extreme learning machine.

eEHR: electronic health record.

fPPG: photoplethysmography.

gECG: electrocardiogram.

hRCT: randomized controlled trial.

iSBP: systolic blood pressure.

jLTSM: long short-term memory.

Emphasizing personalized health care, these studies demonstrate improved accuracy in HTN control by tailoring recommendations to individual patient profiles, challenging traditional one-size-fits-all approaches. One key difference lies in the scale and nature of the datasets used, with some researchers analyzing extensive patient data over extended periods [62], whereas others focus on smaller, more controlled patient groups [59]. In addition, the scope of each study varies; some studies aim to improve BP prediction accuracy, while others focus on optimizing treatment pathways [64], integrating lifestyle data [59], or providing real-time [58] and personalized health care recommendations [59].


Principal Findings

This scoping review provided a comprehensive mapping of the literature on the trends and gaps in digital precision health research for the management of HTN in adults. Analysis of 46 studies identified 3 main categories of precision health focus: personalization, phenotyping, and prediction. The predominance of personalization (34/46, 74% of studies), compared to prediction (8/46, 17%) and phenotyping (4/46, 9%), highlights a strong emphasis on tailored interventions but reveals limited attention to predictive modeling and comprehensive phenotyping, which are essential for predicting HTN outcomes and identifying and categorizing patient subgroups.

Gaps in Digital Precision Health Research

The review revealed geographic, disciplinary, and demographic gaps in digital precision health research for HTN. Most studies (30/46, 65%) reviewed were conducted in the United States, followed by Europe (7/46, 15%), Asia (6/46, 13%), and South America (1/46, 2%), with no studies from Africa or Oceania. This contrasts with high HTN prevalence rates in Africa and Oceania, underscoring the need for more region-specific research to better understand local challenges and develop culturally sensitive and effective strategies for HTN prevention and management [5].

Disciplinary gaps were evident, with >60% (29/46) of the studies originating solely from the medical and health sciences. Less than a third of the studies (15/46) involved interdisciplinary teams, highlighting the need for collaborative efforts across disciplines such as engineering, informatics, and social sciences. Transdisciplinary research, in which team members from diverse fields develop unified conceptual frameworks that transcend their respective disciplinary views, is essential for advancing precision health research in HTN [66].

Demographic reporting was inconsistent and insufficient across studies. While 96% (44/46) of the studies reported participants’ gender and age, 45% (21/46) did not report race and ethnicity, or only did so partially. Of those that reported race and ethnicity, the median percentages of participant representation were skewed heavily toward non-Hispanic White (51%), followed by African American (40%), with underrepresentation of Hispanic or Latinx (5%) and Asian (1%) groups. This lack of diversity raises concerns about generalizability of findings, concern for bias, and underscores the need to for transparency in reporting demographic data, which is especially salient in the context of precision health [67].

Personalized Digital Interventions: Tools, Modalities, and Data Types

Mobile phones were the predominant tools for digital HTN interventions (30/34, 88%), while only 50% (17/34) incorporated home BP monitors and 12% (4/34) used wearable devices. This highlights an opportunity to integrate wearable sensor devices for richer data collection (eg, sleep, heart rate, and physical activity), fostering a more holistic understanding of HTN and its management. Wearable BP monitoring devices is a growing area of research and offers noninvasive, continuous BP monitoring through methods such as photoplethysmography [68]. These devices offer a more comprehensive view of cardiovascular health over time, enabling continuous monitoring, personalized treatment plans, and enhanced predictive capabilities for early intervention. However, further research is needed to enhance their accuracy, calibration, and validation for clinical use [68].

Traditional communication methods such as phone calls and texting were still used (5/30, 17% and 2/30, 7% of studies, respectively), demonstrating their relevance especially for reaching underserved populations with limited digital literacy or access to advanced technology. However, only 20% (6/30) of the studies used multiple intervention delivery modalities (ie, phone calls, texting, and apps), suggesting the need for more integrative approaches to improve access, engagement, and efficacy of digital interventions by catering to different user preferences and needs.

Most studies used behavioral (28/30, 93%), clinical (24/30, 80%), and psychological (17/30, 57%) data for personalization, but only 7% (2/30) of the studies incorporated social determinants such as housing needs or prescription affordability [23,25]. No studies included physical environment or digital literacy data, highlighting key gaps in personalized digital interventions for HTN. Prior studies have documented poor digital literacy and lack of support and training as significant barriers to the use of digital health tools by populations considered disadvantaged [69]. This underscores the need to incorporate diverse sources of data to provide the additional context that can help address disparities in digital intervention engagement and efficacy. Health equity–focused frameworks, such as the Digital Health Equity framework [70], can be used to guide the development and implementation of digital interventions to ensure holistic data collection and personalization, mitigate intervention-generated inequalities, and better address existing health disparities in HTN.

Defining Personalization Strategies

This review identified a critical need for greater clarity and specificity in the use of terminology such as “personalization” or “tailoring” to improve the understanding and application of tailored interventions. As personalization is so broadly defined, it remains challenging to assess the most effective characteristics of personalization for digital interventions. For example, Steinberg et al [48] wrote that “only 28% of participants said they felt the texts were personalized, despite the use of an algorithm designed to personalize messages about intake of specific DASH nutrients.” Such findings indicate the importance of research that specifically delineates which strategies and approaches to personalization are most impactful for users; specifically, there is a need for tools to characterize these approaches to personalization. Fan and Poole [71] provide a useful classification scheme for how personalization can be implemented. Two of the dimensions they describe, in particular, are highly relevant to our corpus: the target of the intervention (either individual or categorical) and the automation approach (either explicit or configured by the user or implicit or automated by the system).

Studies in this review used both individual and categorical targets. For instance, in the study by Kario et al [32], personalization was implemented broadly to group characteristics through tailored BP infographics developed for the target population. This is in contrast to personalization at the individual level, such as in the study by Brewer et al [23], in which participants were assessed for individual social needs and referred for needed services (ie, housing and utilities). While categorical-level personalization strategies can be effective and impactful, we caution against their widespread use in personalization discussions, as precision health primarily focuses on individual-level differences within a patient population. Further research is needed to better understand the characteristics and levels of personalization that are most effective for diverse populations.

In addition, the distinction of whether personalization is automated or human driven is an important lens in understanding an intervention and its effects, and studies in this review leveraged both these approaches as well as hybrid versions of them. While automated models can streamline interventions, they may lack the adaptability of human-led approaches.

Hybrid methods, combining automated and human input, could address the limitations of each approach alone. For example, Schoenthaler et al [46] mentioned the following in their paper: “despite high acceptability, one-third of intervention participants recommended including a health educator as an adjunct to the mHealth intervention, suggesting that some in-person contact is important and could not be replaced by the design of this intervention.” Several papers in our review demonstrate hybrid approaches to personalization, which could guide future research. For example, the intervention developed by Choudhry et al [25] involved a pharmacist-led, semistructured consultation with specific guidelines for mapping barriers to adherence and developing corresponding response strategies. This human-driven, semistructured consultation is paired with automated, system-driven intervention elements, such as SMS text messages. Such hybrid approaches to the design of digital health interventions present a promising avenue for future research.

Digital Phenotyping

The 4 studies focusing on phenotyping within digital precision HTN management illuminate the potential for leveraging a wide spectrum of data—demographic, clinical, behavioral, and genetic—to identify unique phenotypes of participants with HTN to tailor treatment strategies. Multiple study designs, including qualitative interviews and whole-genome analysis, have been used to enhance understanding of HTN. Leveraging secondary data from EHRs and past RCTs for analysis using ML algorithms can help cluster phenotypes of patients with HTN and explain variations in treatment response [72]. Classifying individuals into meaningful groups based on HTN phenotypes is a crucial step toward personalized care and advancing precision health.

By contrast, qualitative approaches, despite having smaller sample sizes, have the ability to provide a more contextual, holistic, and nuanced understanding of the social and psychological determinants of HTN treatment adherence and outcomes from digital interventions, which is crucial for understanding disparities. Future areas of research should integrate the use of multiple sources of data, such as surveys, wearable devices, remote BP monitoring, and ecological momentary assessments, to derive digital phenotypes of participants’ self-management behaviors and provide more effective interventions [73].

Prediction Models

The 8 studies with a precision health focus on prediction models for digital HTN management highlight significant advancements and challenges in the field. These studies collectively demonstrate the innovative use of advanced ML techniques for personalized risk prediction and intervention strategies. Using a wide array of digital tools, including EHR data, wearable devices, mobile platforms, and remote monitoring, these studies are shifting the paradigm beyond one-size-fits-all approaches to care to offer more personalized and preventive care. ML models can help identify factors to predict individuals’ risk of HTN, potentially preventing the development of high BP through early intervention. There are a growing number of studies using diverse ML methods (eg, support vector machine, deep learning, and XGBoost) and data types (eg, genetic, behavioral, and sociodemographic) to accurately predict the development of HTN [74-76].

Despite the potential of prediction models to transform HTN care, these studies also illuminate the hurdles that must be overcome to realize this potential fully. For instance, the generalizability of findings is a significant concern, with varying sample sizes and potential biases from using specific datasets that may not be representative of the population at large. A recent analysis of 63 HTN research studies using ML methods found that only 46% of studies described the participant demographics, and none of the studies provided a rigorous assessment of algorithmic bias, with only 6 studies acknowledging a risk of bias [77]. Algorithmic bias occurs when the diversity of the input dataset used for model development does not match that of the target population, resulting in inaccurate predictions for underrepresented groups and disparities in outcomes [77]. The effectiveness of ML models to accurately predict risk and personalize care relies heavily on the quality of data on which they are trained. The lack of representativeness of participants in training data for these models poses significant concerns regarding their generalizability and potential for bias [67]. To address these limitations, reporting guidelines such as CONSORT-AI (Consolidated Standards of Reporting Trials–Artificial Intelligence) or TRIPOD-AI (Transparent Reporting of a Multivariable Prediction Model for Individual Prognosis or Diagnosis–Artificial Intelligence) should be used when reporting ML prediction models for HTN; these guidelines provide specific criteria for authors to follow, ensuring transparency, completeness, and standardization in study reporting [78,79]. These guidelines emphasize detailed reporting of model development, training, validation, performance metrics, data sources, and patient characteristics which enable comparisons across studies. Furthermore, the prediction models reviewed focused primarily on development, underscoring a key research gap in model deployment and real-world implementation. Advancing precision health in HTN management requires research on best practices for deploying, evaluating, and monitoring models in clinical care.

Strengths and Limitations

This scoping review on digital precision HTN management followed a systematic approach based on the framework developed by Arksey and O’Malley [17], ensuring a rigorous and comprehensive exploration of the field. By adopting a precision health lens, the review covers a broad spectrum of studies, including personalized interventions, prediction models, and phenotyping, offering valuable insights into these areas. The detailed analysis of personalized intervention studies, particularly regarding the characteristics of personalization and data used for personalization, adds depth to the understanding of how digital tools can optimize HTN care. In addition, the interdisciplinary composition of the review team, drawing expertise from nursing, informatics, and computer science, further strengthens this review by incorporating diverse perspectives.

However, the broad scope of this review and the heterogeneity of included studies introduce certain limitations. For example, a detailed examination of intervention effectiveness and statistical significance was limited due to diverse study designs, such as underpowered pilot studies or qualitative designs. The absence of a quality assessment for the included studies may also compromise the validity of the conclusions drawn, as it overlooks methodological rigor and potential biases within studies. Finally, our search terms included “precision health” and only the “personalization” derivatives (eg, precision medicine OR personalized OR tailored OR individualized), which could have limited the number of studies on prediction models or phenotyping. However, the review team chose to include the studies on prediction models and phenotyping as these were considered to be important aspects of precision health research. Future reviews could emphasize a more comprehensive search of these specific aspects of precision health research for digital HTN management.

Conclusions

This scoping review of 46 studies synthesized the current state of precision health research encompassing personalization, phenotyping, and prediction using digital health tools for the management of HTN in adults. The findings from our review demonstrate that the majority (34/46, 74%) of the included studies had a precision health focus of personalization in digital HTN management, followed by prediction models and phenotyping. Our analysis highlighted significant gaps in reporting of participant race and ethnicity data, geographic distribution of research in digital HTN management, and use of wearable devices for capturing passive data. Furthermore, the analysis of personalization characteristics in interventions underscores the need for the integration of multiple sources of data for personalization, such as social determinants of health, physical environment, and digital literacy, to promote health equity. There is a need for more precision in the use of the term “personalization” as well as further research that explores the impact of specific types of personalization on health outcomes. Finally, greater interdisciplinary collaboration and ultimately a transdisciplinary approach are needed to meaningfully advance the field of precision health for HTN risk prediction, prevention, and management.

Acknowledgments

The authors extend their sincere gratitude to Imelda Vetter, health sciences librarian, for her expert guidance in systematic database searches to identify eligible studies for this scoping review. Research reported in this publication was completed with support from the National Institute of Nursing Research of the National Institutes of Health (Award Number T32NR019035, Precision Health Intervention Methodology Training in Self-Management of Multiple Chronic Conditions). The funding agency played no role in the design, data collection, analysis, or writing of the manuscript.

Conflicts of Interest

Authors NC and AA were supported by the National Institute of Nursing Research of the National Institutes of Health (Award Number T32NR019035, Precision Health Intervention Methodology Training in Self-Management of Multiple Chronic Conditions). The funding agency played no role in the design, data collection, analysis, or writing of the manuscript.

Multimedia Appendix 1

PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) checklist.

PDF File (Adobe PDF File), 104 KB

Multimedia Appendix 2

Database search terms.

DOCX File , 17 KB

Multimedia Appendix 3

Characteristics of the included studies.

DOCX File , 50 KB

  1. Hypertension. World Health Organization. Mar 16, 2023. URL: https://www.who.int/news-room/fact-sheets/detail/hypertension [accessed 2024-04-29]
  2. Lawes CM, Vander Hoorn S, Rodgers A, International Society of Hypertension. Global burden of blood-pressure-related disease, 2001. Lancet. May 03, 2008;371(9623):1513-1518. [CrossRef] [Medline]
  3. GBD 2017 Risk Factor Collaborators. Global, regional, and national comparative risk assessment of 84 behavioural, environmental and occupational, and metabolic risks or clusters of risks for 195 countries and territories, 1990-2017: a systematic analysis for the Global Burden of Disease Study 2017. Lancet. Nov 10, 2018;392(10159):1923-1994. [FREE Full text] [CrossRef] [Medline]
  4. NCD Risk Factor Collaboration (NCD-RisC). Worldwide trends in hypertension prevalence and progress in treatment and control from 1990 to 2019: a pooled analysis of 1201 population-representative studies with 104 million participants. Lancet. Sep 11, 2021;398(10304):957-980. [FREE Full text] [CrossRef] [Medline]
  5. Zhou B, Perel P, Mensah GA, Ezzati M. Global epidemiology, health burden and effective interventions for elevated blood pressure and hypertension. Nat Rev Cardiol. Nov 28, 2021;18(11):785-802. [FREE Full text] [CrossRef] [Medline]
  6. Mills KT, Bundy JD, Kelly TN, Reed JE, Kearney PM, Reynolds K, et al. Global disparities of hypertension prevalence and control: a systematic analysis of population-based studies from 90 countries. Circulation. Aug 09, 2016;134(6):441-450. [FREE Full text] [CrossRef] [Medline]
  7. Schutte AE, Jafar TH, Poulter NR, Damasceno A, Khan NA, Nilsson PM, et al. Addressing global disparities in blood pressure control: perspectives of the International Society of Hypertension. Cardiovasc Res. Mar 31, 2023;119(2):381-409. [FREE Full text] [CrossRef] [Medline]
  8. Vrijens B, Vincze G, Kristanto P, Urquhart J, Burnier M. Adherence to prescribed antihypertensive drug treatments: longitudinal study of electronically compiled dosing histories. BMJ. May 17, 2008;336(7653):1114-1117. [FREE Full text] [CrossRef] [Medline]
  9. Hamrahian SM, Maarouf OH, Fülöp T. A critical review of medication adherence in hypertension: barriers and facilitators clinicians should consider. Patient Prefer Adherence. 2022;16:2749-2757. [FREE Full text] [CrossRef] [Medline]
  10. Dzau VJ, Hodgkinson CP. Precision hypertension. Hypertension. Apr 2024;81(4):702-708. [CrossRef]
  11. Minor L, Rees M. Discovering Precision Health: Predict, Prevent, and Cure to Advance Health and Well-Being. Hoboken, NJ. Wiley Blackwell; 2020.
  12. Gambhir SS, Ge TJ, Vermesh O, Spitler R. Toward achieving precision health. Sci Transl Med. Feb 28, 2018;10(430):52. [FREE Full text] [CrossRef] [Medline]
  13. Olstad DL, McIntyre L. Reconceptualising precision public health. BMJ Open. Sep 13, 2019;9(9):e030279. [FREE Full text] [CrossRef] [Medline]
  14. Fu MR, Kurnat-Thoma E, Starkweather A, Henderson WA, Cashion AK, Williams JK, et al. Precision health: a nursing perspective. Int J Nurs Sci. Jan 10, 2020;7(1):5-12. [FREE Full text] [CrossRef] [Medline]
  15. Hickey KT, Bakken S, Byrne MW, Bailey DC, Demiris G, Docherty SL, et al. Precision health: advancing symptom and self-management science. Nurs Outlook. 2019;67(4):462-475. [FREE Full text] [CrossRef] [Medline]
  16. Hekler E, Tiro JA, Hunter CM, Nebeker C. Precision health: the role of the social and behavioral sciences in advancing the vision. Ann Behav Med. Nov 01, 2020;54(11):805-826. [FREE Full text] [CrossRef] [Medline]
  17. Arksey H, O'Malley L. Scoping studies: towards a methodological framework. Int J Soc Res Methodol. Feb 2005;8(1):19-32. [CrossRef]
  18. Braun V, Clarke V. Using thematic analysis in psychology. Qual Res Psychol. Jan 2006;3(2):77-101. [CrossRef]
  19. Kelly TN, Sun X, He KY, Brown MR, Taliun SA, Hellwege JN, et al. Samoan Obesity‚ Lifestyle‚Genetic Adaptations Study (OLaGA) Group‚‡ NHLBI Trans-Omics for Precision Medicine TOPMed) Consortium. Insights from a large-scale whole-genome sequencing study of systolic blood pressure, diastolic blood pressure, and hypertension. Hypertension. Aug 2022;79(8):1656-1667. [FREE Full text] [CrossRef] [Medline]
  20. Beran M, Asche SE, Bergdall AR, Crabtree B, Green BB, Groen SE, et al. Key components of success in a randomized trial of blood pressure telemonitoring with medication therapy management pharmacists. J Am Pharm Assoc (2003). 2018;58(6):614-621. [CrossRef] [Medline]
  21. Blood AJ, Cannon CP, Gordon WJ, Mailly C, MacLean T, Subramaniam S, et al. Results of a remotely delivered hypertension and lipid program in more than 10 000 patients across a diverse health care network. JAMA Cardiol. Jan 01, 2023;8(1):12-21. [FREE Full text] [CrossRef] [Medline]
  22. Bosworth HB, Olsen MK, McCant F, Stechuchak KM, Danus S, Crowley MJ, et al. Telemedicine cardiovascular risk reduction in veterans: the CITIES trial. Am Heart J. May 2018;199:122-129. [CrossRef] [Medline]
  23. Brewer LC, Jones C, Slusser JP, Pasha M, Lalika M, Chacon M, et al. mHealth intervention for promoting hypertension self-management among African American patients receiving care at a community health center: formative evaluation of the FAITH! hypertension app. JMIR Form Res. Jun 16, 2023;7:e45061. [FREE Full text] [CrossRef] [Medline]
  24. Chandler J, Sox L, Kellam K, Feder L, Nemeth L, Treiber F. Impact of a culturally tailored mHealth medication regimen self-management program upon blood pressure among hypertensive Hispanic adults. Int J Environ Res Public Health. Apr 06, 2019;16(7):1226. [FREE Full text] [CrossRef] [Medline]
  25. Choudhry NK, Isaac T, Lauffenburger JC, Gopalakrishnan C, Lee M, Vachon A, et al. Effect of a remotely delivered tailored multicomponent approach to enhance medication taking for patients with hyperlipidemia, hypertension, and diabetes: the STIC2IT cluster randomized clinical trial. JAMA Intern Med. Sep 01, 2018;178(9):1182-1189. [FREE Full text] [CrossRef] [Medline]
  26. David CN, Iochpe C, Harzheim E, Sesin GP, Gonçalves MR, Moreira LB, et al. Effect of mobile health interventions on lifestyle and anthropometric characteristics of uncontrolled hypertensive participants: secondary analyses of a randomized controlled trial. Healthcare (Basel). Apr 08, 2023;11(8):1069. [FREE Full text] [CrossRef] [Medline]
  27. Davidson T, Favella A, McGillicuddy J, Mueller M, Brunner-Jackson B, Anderson A, et al. Evaluation of an mHealth medication regimen self-management program for African American and Hispanic uncontrolled hypertensives. J Pers Med. Nov 17, 2015;5(4):389-405. [FREE Full text] [CrossRef] [Medline]
  28. Glynn L, Casey M, Walsh J, Hayes PS, Harte RP, Heaney D. Patients' views and experiences of technology based self-management tools for the treatment of hypertension in the community: a qualitative study. BMC Fam Pract. Sep 09, 2015;16:119. [FREE Full text] [CrossRef] [Medline]
  29. Guthrie NL, Berman MA, Edwards KL, Appelbaum KJ, Dey S, Carpenter J, et al. Achieving rapid blood pressure control with digital therapeutics: retrospective cohort and machine learning study. JMIR Cardio. Mar 12, 2019;3(1):e13030. [FREE Full text] [CrossRef] [Medline]
  30. Hellem AK, Casetti A, Bowie K, Golbus JR, Merid B, Nallamothu BK, et al. A community participatory approach to creating contextually tailored mHealth notifications: myBPmyLife project. Health Promot Pract. May 27, 2024;25(3):417-427. [CrossRef] [Medline]
  31. Jeong S, Choi H, Gwon SH, Kim J. Telephone support and telemonitoring for low-income older adults. Res Gerontol Nurs. Jul 01, 2018;11(4):198-206. [CrossRef] [Medline]
  32. Kario K, Nomura A, Harada N, Okura A, Nakagawa K, Tanigawa T, et al. Efficacy of a digital therapeutics system in the management of essential hypertension: the HERB-DH1 pivotal trial. Eur Heart J. Oct 21, 2021;42(40):4111-4122. [FREE Full text] [CrossRef] [Medline]
  33. Kassavou A, Mirzaei V, Brimicombe J, Edwards S, Massou E, Prevost AT, et al. A highly tailored text and voice messaging intervention to improve medication adherence in patients with either or both hypertension and type 2 diabetes in a UK primary care setting: feasibility randomized controlled trial of clinical effectiveness. J Med Internet Res. May 19, 2020;22(5):e16629. [FREE Full text] [CrossRef] [Medline]
  34. Klein P, Aebi ME, Sajatovic M, Depp C, Moore D, Blixen C, et al. Differential medication attitudes to antihypertensive and mood stabilizing agents in response to an automated text-messaging adherence enhancement intervention. J Behav Cogn Ther. Apr 2020;30(1):57-64. [FREE Full text] [CrossRef] [Medline]
  35. Leitner J, Chiang PH, Khan B, Dey S. An mHealth lifestyle intervention service for improving blood pressure using machine learning and IoMTs. In: Proceedings of the 2022 IEEE International Conference on Digital Health. 2022. Presented at: ICDH '22; July 10-16, 2022:142-150; Barcelona, Spain. URL: https://ieeexplore.ieee.org/document/9861082 [CrossRef]
  36. Lewinski AA, Patel UD, Diamantidis CJ, Oakes M, Baloch K, Crowley MJ, et al. Addressing diabetes and poorly controlled hypertension: pragmatic mHealth self-management intervention. J Med Internet Res. Apr 09, 2019;21(4):e12541. [FREE Full text] [CrossRef] [Medline]
  37. Lv N, Xiao L, Simmons ML, Rosas LG, Chan A, Entwistle M. Personalized hypertension management using patient-generated health data integrated with electronic health records (EMPOWER-H): six-month pre-post study. J Med Internet Res. Sep 19, 2017;19(9):e311. [FREE Full text] [CrossRef] [Medline]
  38. McBride CM, Morrissey EC, Molloy GJ. Patients' experiences of using smartphone apps to support self-management and improve medication adherence in hypertension: qualitative study. JMIR Mhealth Uhealth. Oct 28, 2020;8(10):e17470. [FREE Full text] [CrossRef] [Medline]
  39. McGillicuddy JW, Gregoski MJ, Weiland AK, Rock RA, Brunner-Jackson BM, Patel SK, et al. Mobile health medication adherence and blood pressure control in renal transplant recipients: a proof-of-concept randomized controlled trial. JMIR Res Protoc. Sep 04, 2013;2(2):e32. [FREE Full text] [CrossRef] [Medline]
  40. Naqvi IA, Strobino K, Kuen Cheung Y, Li H, Schmitt K, Ferrara S, et al. Telehealth after stroke care pilot randomized trial of home blood pressure telemonitoring in an underserved setting. Stroke. Dec 2022;53(12):3538-3547. [CrossRef]
  41. Payne Riches S, Piernas C, Aveyard P, Sheppard JP, Rayner M, Albury C, et al. A mobile health salt reduction intervention for people with hypertension: results of a feasibility randomized controlled trial. JMIR Mhealth Uhealth. Oct 21, 2021;9(10):e26233. [FREE Full text] [CrossRef] [Medline]
  42. Petrella RJ, Stuckey MI, Shapiro S, Gill DP. Mobile health, exercise and metabolic risk: a randomized controlled trial. BMC Public Health. Oct 18, 2014;14:1082. [FREE Full text] [CrossRef] [Medline]
  43. Rodriguez MA, Friedberg JP, Wang B, Fang Y, Natarajan S. Sustain ability of a tailored behavioral intervention to improve hypertension control: outcomes of a randomized controlled trial. J Gen Intern Med. 2015;(7):S261-S262. [FREE Full text]
  44. Rodriguez MA, Friedberg JP, DiGiovanni A, Wang B, Wylie-Rosett J, Hyoung S, et al. A tailored behavioral intervention to promote adherence to the DASH diet. Am J Health Behav. Jul 01, 2019;43(4):659-670. [CrossRef] [Medline]
  45. Saleh S, Farah A, El Arnaout N, Dimassi H, El Morr C, Muntaner C, et al. mHealth use for non-communicable diseases care in primary health: patients' perspective from rural settings and refugee camps. J Public Health (Oxf). Dec 01, 2018;40(suppl_2):ii52-ii63. [FREE Full text] [CrossRef] [Medline]
  46. Schoenthaler A, Leon M, Butler M, Steinhaeuser K, Wardzinski W. Development and evaluation of a tailored mobile health intervention to improve medication adherence in black patients with uncontrolled hypertension and type 2 diabetes: pilot randomized feasibility trial. JMIR Mhealth Uhealth. Sep 23, 2020;8(9):e17135. [FREE Full text] [CrossRef] [Medline]
  47. Shea S, Thompson JL, Schwartz JE, Chen Y, de Ferrante M, Vanderbeek AM, et al. The Retail Outlet Health Kiosk Hypertension Trial (ROKHYT): pilot results. Am J Hypertens. Jan 05, 2022;35(1):103-110. [FREE Full text] [CrossRef] [Medline]
  48. Steinberg DM, Kay MC, Svetkey LP, Askew S, Christy J, Burroughs J, et al. Feasibility of a digital health intervention to improve diet quality among women with high blood pressure: randomized controlled feasibility trial. JMIR Mhealth Uhealth. Dec 07, 2020;8(12):e17536. [CrossRef] [Medline]
  49. Thiboutot J, Sciamanna CN, Falkner B, Kephart DK, Stuckey HL, Adelman AM, et al. Effects of a web-based patient activation intervention to overcome clinical inertia on blood pressure control: cluster randomized controlled trial. J Med Internet Res. Sep 04, 2013;15(9):e158. [FREE Full text] [CrossRef] [Medline]
  50. Van Emmenis M, Jamison J, Kassavou A, Hardeman W, Naughton F, A'Court C, et al. Patient and practitioner views on a combined face-to-face and digital intervention to support medication adherence in hypertension: a qualitative study within primary care. BMJ Open. Feb 28, 2022;12(2):e053183. [FREE Full text] [CrossRef] [Medline]
  51. Wang SQ, Leung M, Leung SY, Han J, Leung W, Hui E, et al. Correction: safety, feasibility, and acceptability of telemedicine for hypertension in primary care: a proof-of-concept and pilot randomized controlled trial (SATE-HT). J Med Syst. Jul 05, 2023;47(1):68. [CrossRef] [Medline]
  52. Willis M, Darwiche G, Carlsson M, Nilsson A, Wohlin J, Lindgren P. Real-world long-term effects on blood pressure and other cardiovascular risk factors for patients in digital therapeutics. Blood Press Monit. Apr 01, 2023;28(2):86-95. [FREE Full text] [CrossRef] [Medline]
  53. Zhang Y, Tao Y, Zhong Y, Thompson J, Rahmani J, Bhagavathula AS, et al. Feedback based on health advice via tracing bracelet and smartphone in the management of blood pressure among hypertensive patients: a community-based RCT trial in Chongqing, China. Medicine (Baltimore). Jul 15, 2022;101(28):e29346. [FREE Full text] [CrossRef] [Medline]
  54. Naqvi IA, Strobino K, Li J, Schmitt K, Garcon M, Li H, et al. Abstract 108: home blood pressure telemonitoring-enhanced versus usual post-acute stroke care in an underserved setting: the telehealth after stroke care pilot randomized clinical trial. Stroke. Feb 2022;53(Suppl_1):33. [CrossRef]
  55. Bakre S, Shea B, Langheier J, Hu EA. Blood pressure control in individuals with hypertension who used a digital, personalized nutrition platform: longitudinal study. JMIR Form Res. Mar 17, 2022;6(3):e35503. [FREE Full text] [CrossRef] [Medline]
  56. Chen R, Sun J, Dittus RS, Fabbri D, Kirby J, Laffer CL, et al. Patient stratification using electronic health records from a chronic disease management program. IEEE J Biomed Health Inform (Forthcoming). Jan 04, 2016. [FREE Full text] [CrossRef] [Medline]
  57. Hellem AK, Whitfield C, Casetti A, Robles MC, Dinh M, Meurer W, et al. Engagement in self-measured blood pressure monitoring among medically underresourced participants (the reach out trial): digital framework qualitative study. JMIR Cardio. Apr 07, 2023;7:e38900. [CrossRef] [Medline]
  58. Bernal SL, Valverde JM, Celdrán AH, Pérez GM. SENIOR: an intelligent web-based ecosystem to predict high blood pressure adverse events using biomarkers and environmental data. Appl Sci. Mar 11, 2021;11(6):2506. [CrossRef]
  59. Chiang PH, Wong M, Dey S. Using wearables and machine learning to enable personalized lifestyle recommendations to improve blood pressure. IEEE J Transl Eng Health Med. 2021;9:1-13. [CrossRef]
  60. Ye XY, Zeng QT, Facelli JC, Brixner DI, Conway M, Bray BE. Predicting optimal hypertension treatment pathways using recurrent neural networks. Int J Med Inform. Jul 2020;139:104122. [FREE Full text] [CrossRef] [Medline]
  61. Abrar S, Loo CK, Kubota N, Tahir GA. A personalised blood pressure prediction system using gaussian mixture regression and online recurrent extreme learning machine. In: Proceedings of the 2020 International Symposium on Community-centric Systems. 2020. Presented at: CcS '20; September 23-26, 2020:23-26; Tokyo, Japan. URL: https://ieeexplore.ieee.org/document/9231328 [CrossRef]
  62. Bertsimas D, Borenstein AR, Dauvin A, Orfanoudaki A. Ensemble machine learning for personalized antihypertensive treatment. Nav Res Logist. Dec 10, 2021;69(5):669-688. [CrossRef]
  63. Cano J, Hornero F, Quesada A, Martinez-Rodrigo A, Alcaraz R, Rieta JJ. Improved discrimination between healthy and hypertensive individuals combining photoplethysmography and electrocardiography. In: Proceedings of the 2021 Conference on Computing in Cardiology. 2021. Presented at: CinC '21; September 13-15, 2021:1-4; Brno, Czech Republic. URL: https://ieeexplore.ieee.org/document/9662894 [CrossRef]
  64. Hu Y, Huerta J, Cordella N, Mishuris RG, Paschalidis IC. Personalized hypertension treatment recommendations by a data-driven model. BMC Med Inform Decis Mak. Mar 01, 2023;23(1):44. [CrossRef] [Medline]
  65. Sun J, McNaughton CD, Zhang P, Perer A, Gkoulalas-Divanis A, Denny JC, et al. Predicting changes in hypertension control using electronic health records from a chronic disease management program. J Am Med Inform Assoc. Mar 01, 2014;21(2):337-344. [FREE Full text] [CrossRef] [Medline]
  66. Mabry PL, Olster DH, Morgan GD, Abrams DB. Interdisciplinarity and systems science to improve population health: a view from the NIH Office of Behavioral and Social Sciences Research. Am J Prev Med. Aug 2008;35(2 Suppl):S211-S224. [CrossRef] [Medline]
  67. Parikh RB, Teeple S, Navathe AS. Addressing bias in artificial intelligence in health care. JAMA. Dec 24, 2019;322(24):2377-2378. [FREE Full text] [CrossRef] [Medline]
  68. Konstantinidis D, Iliakis P, Tatakis F, Thomopoulos K, Dimitriadis K, Tousoulis D, et al. Wearable blood pressure measurement devices and new approaches in hypertension management: the digital era. J Hum Hypertens. Nov 23, 2022;36(11):945-951. [FREE Full text] [CrossRef] [Medline]
  69. Hood CM, Gennuso KP, Swain GR, Catlin BB. County health rankings: relationships between determinant factors and health outcomes. Am J Prev Med. Feb 2016;50(2):129-135. [CrossRef] [Medline]
  70. Richardson S, Lawrence K, Schoenthaler AM, Mann D. A framework for digital health equity. NPJ Digit Med. Aug 18, 2022;5(1):119. [FREE Full text] [CrossRef] [Medline]
  71. Fan H, Poole M. What is personalization? Perspectives on the design and implementation of personalization in information systems. J Organ Comput Electron Commer. 2006:16-202. [CrossRef]
  72. Chaikijurajai T, Laffin LJ, Tang WH. Artificial intelligence and hypertension: recent advances and future outlook. Am J Hypertens. Nov 03, 2020;33(11):967-974. [FREE Full text] [CrossRef] [Medline]
  73. Radhakrishnan K, Kim MT, Burgermaster M, Brown RA, Xie B, Bray MS, et al. The potential of digital phenotyping to advance the contributions of mobile health to self-management science. Nurs Outlook. 2020;68(5):548-559. [CrossRef] [Medline]
  74. Pei Z, Liu J, Liu M, Zhou W, Yan P, Wen S, et al. Risk-predicting model for incident of essential hypertension based on environmental and genetic factors with support vector machine. Interdiscip Sci. Mar 2018;10(1):126-130. [CrossRef] [Medline]
  75. Maxwell A, Li R, Yang B, Weng H, Ou A, Hong H, et al. Deep learning architectures for multi-label classification of intelligent health risk prediction. BMC Bioinformatics. Dec 28, 2017;18(Suppl 14):523. [FREE Full text] [CrossRef] [Medline]
  76. Ye C, Fu T, Hao S, Zhang Y, Wang O, Jin B, et al. Prediction of incident hypertension within the next year: prospective study using statewide electronic health records and machine learning. J Med Internet Res. Jan 30, 2018;20(1):e22. [FREE Full text] [CrossRef] [Medline]
  77. du Toit C, Tran TQ, Deo N, Aryal S, Lip S, Sykes R, et al. Survey and evaluation of hypertension machine learning research. J Am Heart Assoc. May 02, 2023;12(9):e027896. [FREE Full text] [CrossRef] [Medline]
  78. Liu X, Cruz Rivera S, Moher D, Calvert MJ, Denniston AK, SPIRIT-AICONSORT-AI Working Group. Reporting guidelines for clinical trial reports for interventions involving artificial intelligence: the CONSORT-AI extension. Nat Med. Sep 09, 2020;26(9):1364-1374. [FREE Full text] [CrossRef] [Medline]
  79. Collins GS, Moons KG, Dhiman P, Riley RD, Beam AL, Van Calster B, et al. TRIPOD+AI statement: updated guidance for reporting clinical prediction models that use regression or machine learning methods. BMJ. Apr 16, 2024;385:1-14. [FREE Full text] [CrossRef] [Medline]


BP: blood pressure
CONSORT-AI: Consolidated Standards of Reporting Trials–Artificial Intelligence
EHR: electronic health record
HTN: hypertension
ML: machine learning
PRISMA-ScR: Preferred Reporting Items for Systematic Reviews and Meta-Analyses
RCT: randomized controlled trial
TRIPOD-AI: Transparent Reporting of a Multivariable Prediction Model for Individual Prognosis or Diagnosis–Artificial Intelligence


Edited by A Mavragani; submitted 23.04.24; peer-reviewed by N Chapman, WX Lai; comments to author 22.10.24; revised version received 12.11.24; accepted 16.12.24; published 10.02.25.

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©Namuun Clifford, Rachel Tunis, Adetimilehin Ariyo, Haoxiang Yu, Hyekyun Rhee, Kavita Radhakrishnan. Originally published in the Journal of Medical Internet Research (https://www.jmir.org), 10.02.2025.

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