Participant Screening and Consent Sample Clauses

Participant Screening and Consent. The number of patients with uncontrolled HTN approached for participation is tracked as part of the Reach metric of the RE-AIM framework by the research assistant stationed at the practice for recruitment purposes. These data are entered by the research assistant into the study’s web-based data system. Once a participant has expressed interest, the study research assistant screens the prospective participant. For eligible prospective participants, the research assistant then provides an explanation of what participation entails: • Completing a baseline in-person assessment at the practice, • Completing a baseline telephone interview, • Providing several alternative telephone numbers to facilitate contact, • Completing 6-month and 12-month follow-up assessments, • Using a home BP monitor, and • Possibly working with a peer coach. The research assistant also explains randomization, which occurs at the practice level. Willing participants then provide informed consent, which is explained and read to the participants by the research assistant. The study research assistant answers any question the participant may have, and the participant then signs the informed consent (see Appendix 4). A copy of the consent form is provided to the participant. Only trained and quality controlled research assistants provide the information required to obtain informed consent.
Sample 1
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