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

C

Centre hospitalier de l'Université de Montréal (CHUM)

Status

Completed

Conditions

HIV

Treatments

Behavioral: Condom-HIM

Study type

Interventional

Funder types

Other

Identifiers

NCT01726153
R0018767

Details and patient eligibility

About

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

Enrollment

60 patients

Sex

Male

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Web sites
No Intervention group
Description:
Individuals assigned to this arm are given a list of websites where they can view additional information relating to condom use.
Condom-HIM
Experimental group
Description:
Individuals assigned to this arm must follow an on-line one session tailored intervention.
Treatment:
Behavioral: Condom-HIM

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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