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Participants were randomly assigned to the Intervention + Web Booster (N=246) or Intervention + Peer Booster interventions (N=246), or to a control a that did not contain intervention content (N=248).
JMIR Ment Health 2021;8(10):e29397
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As described in a study by Rabbi et al [47], to develop and refine SARA, we conducted (1) a web-based survey to assess user perceptions about design features, (2) focus groups to obtain in-depth qualitative feedback on the app, and (3) a preliminary microrandomized trial (MRT; n=18) to refine app features [47-49].
JMIR Mhealth Uhealth 2021;9(1):e24424
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