A Pilot Trial of an Individualized Web-Based Condom Use Intervention

Not Applicable

Completed

• Conditions: HIV
• Interventions: Behavioral: Condom-HIM

• Registration Number: NCT01726153
• Lead Sponsor: Centre hospitalier de l'Université de Montréal (CHUM)

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Status Verified: 2012-11
• Study Start: 2012-11
• Study First Submitted: 2012-11-06
• Study First Submitted QC: 2012-11-09
• Study First Posted: 2012-11-14
• Primary Completion: 2013-11
• Study Completion: 2014-11
• Last Update Submitted: 2020-07-22
• Last Update Posted: 2020-07-24

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 60

Inclusion Criteria

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

Exclusion Criteria

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Condom-HIM	Condom-HIM	Individuals assigned to this arm must follow an on-line one session tailored intervention.

Primary Outcome Measures

Name	Time	Method
Change from Baseline in participants self-efficacy in condom use at 2-weeks post-intervention	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.

Secondary Outcome Measures

Name	Time	Method
Change from Baseline in participants intention to use condoms at 2-weeks post-intervention	Baseline and 2-weeks post intervention	The intention to use condoms measure asks participants their intention to consistently use condoms. The psychometric properties of the measure have been examined and have shown to have good internal consistency with Cronbach's alpha coefficient of 0.89.

Trial Locations

Locations (1)

Ryerson University; 🇨🇦 Toronto, Ontario, Canada