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

NCT01726153 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2020-07-24

No results posted yet for this study

Summary

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

Conditions

Interventions

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.

Sponsors & Collaborators

  • Centre hospitalier de l'Université de Montréal (CHUM)

    lead OTHER

Principal Investigators

  • Joyal Miranda, PhD · Ryerson University and Centre hospitalier de l'Universite de Montreal (CHUM)

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2013-11-30
Completion
2014-11-30

Countries

  • Canada

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01726153 on ClinicalTrials.gov