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This paper is in the following e-collection/theme issue:

Demographics of Users, Social & Digital Divide (1309) Participatory Medicine & E-Patients (1000) Quality/Credibility of eHealth Information and Trust Issues (947) Participatory Cancer Care (148) Patient Education for Cancer (330) Design and Usability of Websites for Special User Groups (295) Precision Medicine (445) Innovations in Cancer Diagnostic and Decision Support (156)

Published on in Vol 27 (2025)

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/64228, first published .
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Trust and Privacy Concerns Among Cancer Survivors Who Did Not Visit a Research Website Offering Free Genetic Counseling Services for Families: Survey Study

Trust and Privacy Concerns Among Cancer Survivors Who Did Not Visit a Research Website Offering Free Genetic Counseling Services for Families: Survey Study

Authors of this article:

James A Shepperd1 Author Orcid Image ;   Colleen M McBride2 Author Orcid Image ;   Weihua An3 Author Orcid Image ;   Jingsong Zhao2 Author Orcid Image ;   Rebecca D Pentz4 Author Orcid Image ;   Cam Escoffery2 Author Orcid Image ;   Kevin Ward5 Author Orcid Image ;   Yue Guan2 Author Orcid Image
Article Authors Cited by (2) Tweetations Metrics

Journals

  1. Ronan I, Santin O. Strategies to promote the dissemination of psychosocial digital health resources for those affected by cancer: scoping review. Supportive Care in Cancer 2026;34(5) View
  2. Zhao J, McBride C, Shepperd J, An W, Escoffery C, Ward K, Pentz R, Guan Y. Survivors’ Responses to an Online Intervention to Promote Discussions of Cancer Genetic Risk with Blood Relatives. Public Health Genomics 2026;29(1):232 View