Charles R. Drew University of Medicine and Science
Los Angeles, California, 90059, United States
NCT Number: NCT05805306
This is a randomized controlled trial with an attention placebo control group. The goal of this study is to decrease HIV incidence in Latino men who have sex with men by engaging their siblings in PrEP-use promotion. In the intervention arm, siblings will be trained to engage their gay brother in PrEP conversations. In the control arm, siblings will be trained to engage their gay brother in conversations about vaccines to prevent COVID, Hepatitis A/B, or MPOX.
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Notify Me18 year–39 year
All sexes
Interventional
Not applicable
Los Angeles, California, 90059, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Latino Men Who Have Sex with Men
Exclusion criteria
Latino Men Who Have Sex with Men
Inclusion criteria
Siblings
Exclusion criteria
Siblings
The intervention unfolds as follows: (Week 1) the research team, Latino MSM, & sibling will all engage in a PrEP Conversation followed by an individual Sibling Training for siblings to learn communication strategies for promoting health behaviors; (Week 2) we will send siblings reminders and a link to motivational interviewing techniques; (Week 3) we will conduct brief Follow-ups with siblings to determine if their brother changed his behavior; (Week 4) we will send a reminder to Latino MSM that they will have a follow-up the following week; (Week 5) we will conduct 30-day Follow-up with Latino MSM to determine if there was uptake of the new behavior change; (Week 7) same as week 5 above; (Week 10) send siblings information on motivational interviewing; (Week 12) final follow-up for both Latino MSM and siblings.
The intervention unfolds as follows: (Week 1) the research team, Latino MSM, & sibling will all engage in a Health Conversation about vaccines for COVID, Hep A/B, or MPOX, followed by an individual Sibling Training for siblings to learn communication strategies for promoting health behaviors; (Week 2) we will send siblings reminders and a link to motivational interviewing techniques; (Week 3) we will conduct brief Follow-ups with siblings to determine if their brother changed his behavior; (Week 4) we will send a reminder to Latino MSM that they will have a follow-up the following week; (Week 5) we will conduct 30-day Follow-up with Latino MSM to determine if there was uptake of the new behavior change; (Week 7) same as week 5 above; (Week 10) send siblings information on motivational interviewing; (Week 12) final follow-up for both Latino MSM and siblings.
Time frame: 90 days
This measures how many participants in the experiment group started taking PrEP (baseline = 0 participants).
Tool: Pictures. Participants will submit a picture of their pill bottle to report PrEP use.
Time frame: 90 days
This measures whether participants in the control group decided to get vaccinated for COVID, Hep A/B, or MPOX.
Tool: Pictures. Participants will submit a picture of their proof-of-vaccination card to report vaccination status.
Time frame: 90 days
This measures whether participants progress along the stages of change (e.g., pre-contemplation, contemplation, action) in their willingness to try PrEP if it were available to them.
Tool: Stages of Change questionnaire administered at baseline and 90 days.
Time frame: 90 days
This measures whether participants progress along the stages of change (e.g., pre-contemplation, contemplation, action) in their willingness to get vaccinated against COVID, Hep A/B, or MPOX if it were available to them.
Tool: Stages of Change questionnaire administered at baseline and 90 days.
Charles Drew University of Medicine and Science
Other
Promoting HIV PrEP Among MSM: a Randomized Control Trial - Aim 3
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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