Medication Adherence Clinical Trial
Official title:
A Mobile Phone Intervention Using a Relational Human Talking Avatar to Promote Multiple Stages of the HIV Care Continuum in African American MSM
The investigators propose to determine the efficacy of "My Personal Health Guide," a theory-based innovative talking relational human Avatar mobile phone application to engage HIV-positive AAMSM in adherence and retention in care. Providing an empathetic talking Avatar source of HIV-related information, motivation, and behavioral skills that is as private and convenient as their own mobile phone might produce a high impact by overcoming barriers to HIV adherence and retention in care such as stigma and health literacy.
Status | Recruiting |
Enrollment | 295 |
Est. completion date | November 30, 2023 |
Est. primary completion date | July 31, 2023 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 18 Years to 34 Years |
Eligibility | Inclusion Criteria: - Self-reported African American MSM - 18 to 34 years old - Smartphone owners - Prescribed ART - Have a viral load detectable within the past 4 weeks or self-reported or provider-reported history of adherence or treatment engagement problems. - Participants may be initiating ART or already on ART. Exclusion Criteria: - Cannot speak English - Decline to participate - Participated in the usability and Beta testing phase of the app refinement that preceded this RCT - Do not have a routine clinic appointment scheduled during the observation time. |
Country | Name | City | State |
---|---|---|---|
United States | University of Illinois at Chicago | Chicago | Illinois |
Lead Sponsor | Collaborator |
---|---|
University of Illinois at Chicago | Emory University, National Institute of Mental Health (NIMH), Ruth M. Rothstein CORE Center, University of Mississippi Medical Center |
United States,
Dworkin M, Chakraborty A, Lee S, Monahan C, Hightow-Weidman L, Garofalo R, Qato D, Jimenez A. A Realistic Talking Human Embodied Agent Mobile Phone Intervention to Promote HIV Medication Adherence and Retention in Care in Young HIV-Positive African American Men Who Have Sex With Men: Qualitative Study. JMIR Mhealth Uhealth. 2018 Jul 31;6(7):e10211. doi: 10.2196/10211. — View Citation
Dworkin MS, Lee S, Chakraborty A, Monahan C, Hightow-Weidman L, Garofalo R, Qato DM, Liu L, Jimenez A. Acceptability, Feasibility, and Preliminary Efficacy of a Theory-Based Relational Embodied Conversational Agent Mobile Phone Intervention to Promote HIV Medication Adherence in Young HIV-Positive African American MSM. AIDS Educ Prev. 2019 Feb;31(1):17-37. doi: 10.1521/aeap.2019.31.1.17. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Viral suppression | The investigators will review medical records for HIV viral load measurements including the detectable measurement at study entry and all measurements that occur during the 6 months of follow-up and 2 months after. To ensure a high proportion of subjects have a follow-up viral load for comparison to their study entry viral load, the investigators will collect a fingerprick dried blood spot for viral load at the follow-up interview. | From study enrollment until 2 months after study conclusion (9 months). | |
Secondary | Antiretroviral therapy adherence | The investigators will use the Wisepill real-time electronic monitoring adherence device. The device obtains daily adherence information that can be analyzed as 7 monthly adherence measurements (1 month baseline and 6 months follow-up) calculated as proportion of doses taken out of days in the month. To supplement this measure, in the follow-up questionnaire the investigators will also collect the number of missed doses during the past month by self-report. | 6 months before enrollment through two months after study conclusion (15 months). | |
Secondary | Retention in care | To measure retention in care, the investigators will query participant's medical record to determine the number of HIV-related visits during the 6-months of follow-up. | From app installation until study conclusion (6 months). |
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