CompletedNot Applicable

Acceptability, Feasibility, and Preliminary Impact of a Web-based, HIV Prevention Toolkit With Cisgender Male Couples in Lima, Peru

United States148 participantsStarted 2022-12-27

Plain-language summary

This digital couples-based HIV/STI prevention intervention project will determine preliminary efficacy to improve uptake of evidence-based strategies and a tailored prevention plan among cisgender male couples who are in a relationship (defined as greater than 3 months or more).

Who can participate

Age range18 Years

SexMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. being assigned male at birth and currently identifying as male (cis-gender);
✓. having had anal sex with each other in the past 3 months;
✓. referring to each other as being in a relationship, defined as "someone you feel emotionally or romantically committed to above all others, and may be referred to as partner, husband, partner, etc.";
✓. being in a relationship with each other for 3 months or longer;
✓. being at least 18 years of age;
✓. not having any history of intimate partner violence since their relationship began;
✓. self-reporting not feeling coerced by their partner to take part in the study activities;
✓. having their own Internet/web-connected device (e.g. smartphone, laptop, tablet, computer);

Exclusion criteria

✕Does not meet one or more of the inclusion criteria

What they're measuring

Changes in the creation of a detailed risk reduction plan by comparing responses from baseline to 3-months, 3-months to 6-months, and baseline to 6-months.

Timeframe: baseline to 3-months, 3-months to 6-months, and baseline to 6-months

Changes in the creation of a detailed agreement by comparing responses from baseline to 3-months, 3-months to 6-months, and baseline to 6-months.

Timeframe: baseline to 3-months, 3-months to 6-months, and baseline to 6-months.

Changes in adherence to risk-reduction plan by comparing responses from baseline to 3-months, 3-months to 6-months, and baseline to 6-months.

Timeframe: baseline to 3-months, 3-months to 6-months, and baseline to 6-months.

Changes in adherence to agreement by comparing responses from baseline to 3-months, 3-months to 6-months, and baseline to 6-months.

Timeframe: baseline to 3-months, 3-months to 6-months, and baseline to 6-months

Changes in the number of evidence-based prevention strategies being used over time by comparing responses from baseline to 3-months, 3-months to 6-months, and baseline to 6-months.

Timeframe: baseline to 3-months, 3-months to 6-months, and baseline to 6-months

Change in HIV incidence by comparing results from testing at baseline to 6-months.

Timeframe: baseline to 6 months

Trial details

NCT IDNCT05873855

SponsorFlorida International University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-04-26

View on ClinicalTrials.gov More HIV Infections trials

Who can participate

Age range18 Years

SexMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. being assigned male at birth and currently identifying as male (cis-gender);
✓. having had anal sex with each other in the past 3 months;
✓. referring to each other as being in a relationship, defined as "someone you feel emotionally or romantically committed to above all others, and may be referred to as partner, husband, partner, etc.";
✓. being in a relationship with each other for 3 months or longer;
✓. being at least 18 years of age;
✓. not having any history of intimate partner violence since their relationship began;
✓. self-reporting not feeling coerced by their partner to take part in the study activities;
✓. having their own Internet/web-connected device (e.g. smartphone, laptop, tablet, computer);

Exclusion criteria

✕Does not meet one or more of the inclusion criteria