CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 673 enrolled
Drug / intervention
Survey +2 moreother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03360422
NCT03360422N/ACompleted

Advancing New Computer-based Health Outcomes Regarding Sexual Behavior(ANCHORS) Study: UH2 Project

University of Florida·interventional·Posted Dec 4, 2017·Updated Jul 11, 2024

In Brief

A clinical study evaluating Survey, Focus Group, and 1 other intervention for HIV-1-infection. Completed, enrolled 673 participants across 1 site.

Detailed Summary

According to the National HIV/AIDS Strategy, men who have sex with men (MSM), young adults, Black and Latino men and people in the Southern U.S. are at highest HIV risk and should be targeted with cost-effective, scalable interventions. The study team propose a synergistic mobile intervention to reduce alcohol and HIV risk in young adult MSM that combines 3 efficacious approaches.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHIV-1-infection
CountriesUnited States

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedDec 4, 2017
Enrollment StartDec 1, 2017
Primary CompletionJun 19, 2020
Study CompletionJul 1, 2023
TodayJul 2, 2026
Enrollment to primary: 2.6 yearsPosted 8.6 years ago

Interventions

Surveyother

Respondents meeting inclusion criteria will be informed they were selected for the longer survey and continue to the survey. Upon completion, the survey will generate a study identification (ID) that respondents will provide to study staff with additional contact information via phone, text or email to be compensated

Focus Groupother

After informed consent, participants will complete the web-based intervention component in development. Afterward, participants will be engaged by an experienced facilitator in a discussion of aspects of the intervention they liked and disliked and suggestions they have for enhancing its cultural appropriateness to young MSM.

Usability studyother

After informed consent, participants will utilize the mobile intervention in development for 30 days to establish usability, acceptability and correct any functionality issues.