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Completed

NCT Number: NCT01726153

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

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

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Key information

Conditions

HIV

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

Ryerson University

Toronto, Ontario, M5B 2K3, Canada

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

-

Treatment and study plan

Condom-HIM

Behavioral

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.

Primary outcomes

  1. 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.

Secondary outcomes

  1. Change from Baseline in participants intention to use condoms at 2-weeks post-intervention

    Time frame: 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.

Other outcomes

  1. Change from Baseline in participants condom use at 2-weeks post-intervention Condom Use

    Time frame: baseline and 2-weeks post intervention

Sponsors and collaborators

Lead sponsor

Centre hospitalier de l'Université de Montréal (CHUM)

Other

Registry information

Official study title

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

Important dates

Study start
2012
Primary completion
2013
Study completion
2014
First posted
Nov 14, 2012
Registry last updated
Jul 24, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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