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

HIV Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01726153
• Other study ID #: R0018767
• Status: Completed
• Phase: N/A
• Start date: November 2012
• Est. completion date: November 2014

Study information

• Verified date: November 2012
• Source: Centre hospitalier de l'Université de Montréal (CHUM)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: November 2014
• Est. primary completion date: November 2013
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years and older

Eligibility

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:

-

Related Conditions & MeSH terms

• HIV

Intervention

Behavioral:
• Condom-HIM
The tailored on-line Condom-HIM intervention is composed of a single session involving activities to increase individuals self-efficacy and intention to use condoms.

Locations

Country	Name	City	State
Canada	Ryerson University	Toronto	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
Centre hospitalier de l'Université de Montréal (CHUM)

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change from Baseline in participants condom use at 2-weeks post-intervention Condom Use		baseline and 2-weeks post intervention
Primary	Change from Baseline in participants self-efficacy in condom use at 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.	baseline and 2-weeks post intervention
Secondary	Change from Baseline in participants intention to use condoms at 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.	Baseline and 2-weeks post intervention