A Pilot Randomized Control Trial (RCT) of an Individualized Condom-HIM Web-based Intervention for Condom USe Among HIV+ Gay Males

Centre hospitalier de l'Université de Montréal (CHUM)1 site in 1 country60 target enrollmentNovember 2012

ConditionsHIV

Overview

Phase: N/A
Intervention: Not specified
Conditions: HIV
Sponsor: Centre hospitalier de l'Université de Montréal (CHUM)
Enrollment: 60
Locations: 1
Primary Endpoint: Change from Baseline in participants self-efficacy in condom use at 2-weeks post-intervention
Status: Completed
Last Updated: 5 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

The purpose of this study is to evaluate the efficacy of an online intervention in increasing condom use among HIV+ gay males.

Registry

clinicaltrials.gov

Start Date

November 2012

End Date

November 2014

Last Updated

5 years ago

Study Type

Interventional

Study Design

Parallel

Sex

Male

Investigators

Sponsor

Centre hospitalier de l'Université de Montréal (CHUM)

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•are HIV-seropositive,
•Men who are having sex with men,
•engaging in unprotected anal intercourse with a partner who is serostatus negative or unknown
•age 18 years and older,
•ability to read English
•have access to a computer and internet.

Exclusion Criteria

Not provided

Outcomes

Primary Outcomes

Change from Baseline in participants self-efficacy in condom use at 2-weeks post-intervention

Time Frame: baseline and 2-weeks post intervention

The Self-Efficacy for condom use measure contains a set of items to rate participant's belief that they will be able to use condoms every time they have anal sex in a variety of situations. A four-point response scale, ranging from 'strongly agree' (0) to 'strongly disagree' (4) is used. The psychometric properties of the measure have been examined and have been shown to have good internal consistency with Cronbach's alpha coefficient of 0.96.