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Feasibility and Cultural Adaptation of a Community-Engaged Physical Activity Intervention for Hispanic Older Adults: Pilot Study

Feasibility and Cultural Adaptation of a Community-Engaged Physical Activity Intervention for Hispanic Older Adults: Pilot Study

Participants were between the ages of 55 and 70 years, 90% (n=9) were women, 90% preferred Spanish (n=9), and they had a mean education of 11.8 (SD 3.8) years (Table 1). Pre-post pilot participant characteristics (N=10). a Some values are missing from the participant characteristics table due to participant nonresponse: education (n=2); race (n=1); employment status (n=1), and high cholesterol (n=1). All health indicators are based on participant self-report during the baseline screening phone call.

Zvinka Z Zlatar, Mikael Anne Greenwood-Hickman, Lazaro N Martinez Lujan, Julie Cooper, Stefani Florez-Acevedo, David X Marquez, Rosa Gutierrez Aceves, Andrea Paula Vargas, Dori E Rosenberg

JMIR Form Res 2025;9:e65489

Developing a Core Outcome Set for Pediatric and Adult Acute and Chronic Pain Extended Reality Trials: Delphi Consensus-Building Process

Developing a Core Outcome Set for Pediatric and Adult Acute and Chronic Pain Extended Reality Trials: Delphi Consensus-Building Process

A total of 194 articles were included in data extraction (n=104, 53.6% adult; n=90, 46.4% pediatric), with 4 studies being coded as both pediatric and adult given that the study sample spanned both populations.

Courtney W Hess, Deirdre E Logan, Brittany N Rosenbloom, Giulia Mesaroli, Laura E Simons, Carley Ouellette, Cynthia Nguyen, Fahad Alam, Jennifer N Stinson

J Med Internet Res 2025;27:e58947

Size and Composition of Caregiver Networks Who Manage Medications for Persons Living With Dementia: Cross-Sectional Analysis of the 2011-2022 National Health and Aging Trends Study

Size and Composition of Caregiver Networks Who Manage Medications for Persons Living With Dementia: Cross-Sectional Analysis of the 2011-2022 National Health and Aging Trends Study

Among non-Hispanic White caregivers who manage medications (n=1633), the mean number of participants assisting with medications was 2.4 (range 1-9). Caregivers who helped with medications were 17.3% (282/1633) spouses, 33.9% (555/1633) children, 2.9% (48/1633) grandchildren, 9.6% (157/1633) others, 35.5% (580/1633) paid helpers, and 0.7% (11/1633) siblings. Among Black or African American caregivers (n=799), the mean number of caregivers assisting with medications was 2.8 (range 1-9).

Reed WR Bratches, Frank Puga, Paul J Barr, Amanda N Leggett, Meredith Masel, James Nicholas Odom, Rita Jablonski

Interact J Med Res 2025;14:e64499

The American Transformative HIV Study: Protocol for a US National Cohort of Sexual and Gender Minority Individuals With HIV

The American Transformative HIV Study: Protocol for a US National Cohort of Sexual and Gender Minority Individuals With HIV

We aimed to enroll a cohort of participants at high risk for HIV that was geographically diverse (ie, with representation from every US state), racially and ethnically diverse (n=3031, 56.5% are participants of color), and young (n=1704, 31.8% aged 16‐29 years). We overenrolled persons who reported recent ( Enrollment for AMETHST began in August 2022 and concluded in August 2023. Participants were recruited via advertisements on men-for-men geosocial sexual networking mobile phone apps.

Christian Grov, Alexa B D'Angelo, Chloe Mirzayi, Michelle Dearolf, Elena Hoeppner, Yan Guo, Nicole Richards, Rifa Ehsan, Sarah Kulkarni, Denis Nash, Viraj V Patel, Dustin T Duncan, Meredith Ray, Tyler Bartholomew, Jennifer Manuzak, Jennifer Manuel, Kathryn McCollister, Drew Westmoreland, Adam W Carrico

JMIR Public Health Surveill 2025;11:e66921

Toward a Domain-Overarching Metadata Schema for Making Health Research Studies FAIR (Findable, Accessible, Interoperable, and Reusable): Development of the NFDI4Health Metadata Schema

Toward a Domain-Overarching Metadata Schema for Making Health Research Studies FAIR (Findable, Accessible, Interoperable, and Reusable): Development of the NFDI4Health Metadata Schema

The majority of these resources were studies (n=243), data dictionaries (n=143), questionnaires (n=78), substudies (n=49), and other data collection instruments (n=35). Remaining resources included datasets (n=19), manuals of operations (SOPs; n=15), other study documents (n=15), registries or secondary data sources (n=9), case report forms (n=5), codebooks (n=5), interview schemes and themes (n=4), data management plans (n=3), other resource types (n=2), and statistical analysis plans (n=1).

Haitham Abaza, Aliaksandra Shutsko, Sophie A I Klopfenstein, Carina N Vorisek, Carsten Oliver Schmidt, Claudia Brünings-Kuppe, Vera Clemens, Johannes Darms, Sabine Hanß, Timm Intemann, Franziska Jannasch, Elisa Kasbohm, Birte Lindstädt, Matthias Löbe, Katharina Nimptsch, Ute Nöthlings, Marisabel Gonzalez Ocanto, Tracy Bonsu Osei, Ines Perrar, Manuela Peters, Tobias Pischon, Ulrich Sax, Matthias B Schulze, Florian Schwarz, Carolina Schwedhelm, Sylvia Thun, Dagmar Waltemath, Hannes Wünsche, Atinkut A Zeleke, Wolfgang Müller, Martin Golebiewski

JMIR Med Inform 2025;13:e63906