Development of a Tailored HIV Prevention Intervention for Young Men



Status:Completed
Conditions:HIV / AIDS
Therapuetic Areas:Immunology / Infectious Diseases
Healthy:No
Age Range:18 - 24
Updated:5/11/2017
Start Date:November 2016
End Date:May 2017

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This study uses an interactive design and development process to develop tailored messages
that align YMSM's relationship experiences and desires with HIV prevention strategies. The
study includes a tailored online prevention, intervention, as well as an attention control
non--tailored HIV prevention (NTHP) comparison intervention. The pilot RCT will compare the
intervention (N=120) to NTHP (N=60) to assess intervention feasibility and acceptability,
and gather preliminary behavioral data to inform a subsequent application. Follow-up
assessments will be collected at thirty (30), sixty (60), and ninety (90) days
post-intervention.

A resurgence of new HIV cases among young men who have sex with men (YMSM; ages 18--24) has
underscored the importance of developing culturally- and developmentally- informed HIV
programs for YMSM. The investigators are developing and pilot testing a tailored, web- based
intervention called myDEx that focuses on delivering HIV prevention messages based on single
YMSM's relationship expectations and partner--seeking behaviors. To maximize intervention
appeal and appropriateness, the investigators have convened a youth advisory board (YAB) to
provide insight and feedback during the 3--stage intervention development process. Using an
iterative design and development process, they have developed tailored messages that align
YMSM's relationship experiences and desires with HIV prevention strategies. The
investigators designed and developed the myDEx tailored online prevention intervention, as
well as an attention- control non--tailored HIV/AIDS prevention (NTHP) comparison
intervention. After developing both interventions, the investigators used usability testing
procedures to collect preliminary data from 16 YMSM on the proposed intervention's design
and acceptability. Recommended changes were added to the intervention prior to launching a
small pilot randomized controlled trial (RCT). The pilot RCT will compare myDEx (N=120) to
NTHP (N=60) to assess intervention feasibility and acceptability, and gather preliminary
behavioral data to inform a subsequent application. Assessments will be collected at 30, 60,
and 90 days follow--up.

Specific Aims include:

1. To develop a tailored (myDEx) and non-tailored (NTHP) HIV prevention intervention
focused on addressing HIV risk behaviors among single YMSM;

2. To collect preliminary data on the feasibility, acceptability, and intervention content
of the myDEx (N=16) in preparation for a small pilot RCT; and,

3. To implement a small pilot RCT of the refined myDEx (N=120) as compared to the NTHP
(N=60) intervention, in order to evaluate its feasibility and acceptability and gather
preliminary efficacy results in reducing sexual risk behaviors.

Inclusion Criteria:

- Cis-gender male

- Self-report as being single

- Self report as HIV-negative at baseline

- Speak and read English

- Report unprotected anal intercourse with a male partner in prior six (6) months

- Have access to computer or smartphone device

Exclusion Criteria:

- Transgender identity

- HIV positive diagnosis

- Not residing in the United States

- Does not engage in male-to-male sexual behavior
We found this trial at
1
site
3451 Walnut St
Philadelphia, Pennsylvania 19104
1 (215) 898-5000
Principal Investigator: Jose A Bauermeister, PhD
Phone: 215-898-9993
Univ of Pennsylvania Penn has a long and proud tradition of intellectual rigor and pursuit...
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