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Tytuł pozycji:

Increasing HIV Testing and Viral Suppression via Stigma Reduction in a Social Networking Mobile Health Intervention Among Black and Latinx Young Men and Transgender Women Who Have Sex With Men (HealthMpowerment): Protocol for a Randomized Controlled Trial

Tytuł:
Increasing HIV Testing and Viral Suppression via Stigma Reduction in a Social Networking Mobile Health Intervention Among Black and Latinx Young Men and Transgender Women Who Have Sex With Men (HealthMpowerment): Protocol for a Randomized Controlled Trial
Autorzy:
Muessig, Kathryn Elizabeth
Golinkoff, Jesse M
Hightow-Weidman, Lisa B
Rochelle, Aimee E
Mulawa, Marta I
Hirshfield, Sabina
Rosengren, A Lina
Aryal, Subhash
Buckner, Nickie
Wilson, M Skye
Watson, Dovie L
Houang, Steven
Bauermeister, José Arturo
Temat:
Medicine
Computer applications to medicine. Medical informatics
R858-859.7
Źródło:
JMIR Research Protocols, Vol 9, Iss 12, p e24043 (2020)
Wydawca:
JMIR Publications, 2020.
Rok publikacji:
2020
Kolekcja:
LCC:Medicine
LCC:Computer applications to medicine. Medical informatics
Typ dokumentu:
article
Opis pliku:
electronic resource
Język:
English
ISSN:
1929-0748
Relacje:
https://www.researchprotocols.org/2020/12/e24043; https://doaj.org/toc/1929-0748
DOI:
10.2196/24043
Dostęp URL:
https://doaj.org/article/e16a80ab71a74c4c887e6d308b10f9e7  Link otwiera się w nowym oknie
Numer akcesji:
edsdoj.16a80ab71a74c4c887e6d308b10f9e7
Czasopismo naukowe
BackgroundStigma and discrimination related to sexuality, race, ethnicity, and HIV status negatively impact HIV testing, engagement in care, and consistent viral suppression (VS) among young Black and Latinx men who have sex with men and transgender women who have sex with men (YBLMT). Few interventions address the effects of intersectional stigma among youth living with HIV and those at risk for HIV within the same virtual space. ObjectiveBuilding on the success of the HealthMpowerment (HMP) mobile health (mHealth) intervention (HMP 1.0) and with the input of a youth advisory board, HMP 2.0 is an app-based intervention that promotes user-generated content and social support to reduce intersectional stigma and improve HIV-related outcomes among YBLMT. The primary objective of this study is to test whether participants randomized to HMP 2.0 report improvement in HIV prevention and care continuum outcomes compared with an information-only control arm. We will also explore whether participant engagement, as measured by paradata (data collected as users interact with an mHealth intervention, eg, time spent using the intervention), mediates stigma- and HIV care–related outcomes. Finally, we will assess whether changes in intersectional stigma and improvements in HIV care continuum outcomes vary across different types of social networks formed within the intervention study arms. MethodsWe will enroll 1050 YBLMT aged 15 to 29 years affected by HIV across the United States. Using an HIV-status stratified, randomized trial design, participants will be randomly assigned to 1 of the 3 app-based conditions (information-only app-based control arm, a researcher-created network arm of HMP 2.0, or a peer-referred network arm of HMP 2.0). Behavioral assessments will occur at baseline, 3, 6, 9, and 12 months. For participants living with HIV, self-collected biomarkers (viral load) are scheduled for baseline, 6, and 12 months. For HIV-negative participants, up to 3 HIV self-testing kits will be available during the study period. ResultsResearch activities began in September 2018 and are ongoing. The University of Pennsylvania is the central institutional review board for this study (protocol #829805) with institutional reliance agreements with the University of North Carolina at Chapel Hill, Duke University, and SUNY Downstate Health Sciences University. Study recruitment began on July 20, 2020. A total of 205 participants have been enrolled as of November 20, 2020. ConclusionsAmong a large sample of US-based YBLMT, this study will assess whether HMP 2.0, an app-based intervention designed to ameliorate stigma and its negative sequelae, can increase routine HIV testing among HIV-negative participants and consistent VS among participants living with HIV. If efficacious and brought to scale, this intervention has the potential to significantly impact the disproportionate burden of HIV among YBLMT in the United States. Trial RegistrationClinicalTrials.gov NCT03678181; https://clinicaltrials.gov/ct2/show/study/NCT03678181. International Registered Report Identifier (IRRID)DERR1-10.2196/24043

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