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Clinical Trials/NCT04417946
NCT04417946
Completed
Not Applicable

Peer-led Social Media Intervention to Prevent HIV Among Young Men Who Have Sex With Men (YMSM)

Yale University2 sites in 1 country227 target enrollmentJune 5, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pre-Exposure Prophylaxis
Sponsor
Yale University
Enrollment
227
Locations
2
Primary Endpoint
PrEP uptake
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to examine the effect of social media intervention on the use of pre-exposure prophylaxis (PrEP) by young men who have sex with men (YMSM) in the greater New Haven area.

Detailed Description

There are three specific aims of this study. In the first specific aim, two focus group discussions (FGDs) of YMSM will be conducted to assess the feasibility and acceptability of social media intervention. In the second specific aim of the study, a quasi-pre-post experimental study will be conducted to examine the effect of social media intervention on PrEP uptake (primary outcome) and PrEP use intention, HIV testing, PrEP knowledge, self-efficacy and social support (secondary outcome). In the third specific aim of the study, the most important topics around PrEP will be assessed on the Facebook page of the intervention group by conducting a content analysis.

Registry
clinicaltrials.gov
Start Date
June 5, 2018
End Date
April 1, 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Male

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Biologically male or transgender man
  • Self-identification as gay or bi-sexual
  • Resident of greater New Haven area
  • Willing and able to use Facebook during the span of the study

Exclusion Criteria

  • • Women will not be included in the study
  • Under the age of 18 and over the age of 29
  • Unable to provide informed consent
  • Verbally or physically threatening to research staff

Outcomes

Primary Outcomes

PrEP uptake

Time Frame: PrEP uptake (Yes/No) at 24-weeks

Actual PrEP uptake: participants self report if they use prep (Yes/No)

Secondary Outcomes

  • PrEP use intention(PrEP use intention at 24-weeks)
  • HIV testing(24-weeks)
  • self efficacy to use PrEP(self efficacy to use PrEP at 24-weeks)
  • motivation to use PrEP(motivation to use PrEP at 24-weeks)
  • PrEP stigma(PrEP stigma at 24-weeks)
  • PrEP knowledge(PrEP knowledge at 24-weeks)
  • Social support for PrEP use(Social support for PrEP use at 24-weeks)

Study Sites (2)

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