4.5 Article

Leave me out: Patients' characteristics and reasons for opting out of a pragmatic clinical trial involving medication adherence

期刊

MEDICINE
卷 100, 期 51, 页码 -

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MD.0000000000028136

关键词

clinical trial methodology; informed consent; patient centered outcomes research; population health; pragmatic clinical trial; research activities; veteran health

资金

  1. National Institutes of Health (NIH) Health Care Systems Research Collaboratory from the National Heart, Lung, and Blood Institute [UG3HLD144163]
  2. NIH Health Care Systems Research Collaboratory by the NIH Common Fund from the Office of Strategic Coordination within the Office of the NIH Director [U24AT009676]

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In a pragmatic clinical trial evaluating the effect of text messages on medication adherence, 10% of patients opted out of participation. Those who opted out tended to be older, white, and non-Hispanic. Survey results showed that a high level of trust in healthcare providers, research, and the system influenced patients' decision to opt-out, with time concerns being a common reason for opting out.
Opt-out procedures are sometimes used instead of standard consent practices to enable patients to exercise their autonomous preferences regarding research participation while reducing patient and researcher burden. However, little is known about the characteristics of patients who opt-out of research and their reasons for doing so. We gathered such information in a large pragmatic clinical trial (PCT) evaluating the effect of theory informed text messages on medication adherence. Eligible patients, identified through electronic health records, were sent information about the study and provided with an opportunity to opt-out. Those opting out were asked to complete a voluntary survey regarding their reasons for doing so. Demographic data were compared among patients opting-out vs those included in the study using chi-squared tests and a log binomial regression model. Of 9046 patients receiving study packets, 906 (10.0%) patients returned opt-out forms. Of those, 451 (49.8%) returned the opt-out survey. Patients who opted out were more likely to be older, white, and nonHispanic than those who were included in the PCT. Survey respondents expressed high levels of trust in their health care providers, research, and system. Nearly half (46.6%) reported concerns about time as a reason to opt-out. In this PCT, 10% of patients receiving packets opted out, with significant differences in age, race, gender, and ethnicity compared to those included. Future trials should further investigate representativeness and reasons patients choose to opt-out of participating in research.

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