Online Consent Enables a Randomized, Controlled Trial Testing a Patient-Centered Online Decision-Aid for Medicare Beneficiaries to Meet Recruitment Goal in Short Time Frame

Author:

Meehan Amy1ORCID,Bundorf Mary Kate2,Klimke Roman2,Stults Cheryl D.1,Chan Albert S13,Pun Ting4,Tai-Seale Ming15

Affiliation:

1. Palo Alto Medical Foundation Research Institute, Palo Alto, CA, USA

2. Department of Health Research and Policy, Stanford University, Stanford, CA, USA

3. Sutter Health, San Carlos, CA, USA

4. Patient-Centered Outcomes Research Institute Patient Advisory Council, Portola Valley, CA, USA

5. University of California San Diego School of Medicine, La Jolla, CA, USA

Abstract

Online consenting allows potential participants of research projects to deliberate their participation at their own pace and may be more cost-effective than conventional approaches. Yet, online consenting is not widespread in health services research due partly to concerns about security, confidentiality, and lack of established processes. We report our use of online consenting to successfully enroll over 1185 Medicare beneficiaries in a short 9-week time frame for a research study.

Funder

Patient-Centered Outcomes Research Institute

Publisher

SAGE Publications

Subject

Health Policy,Health (social science),Leadership and Management

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