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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-11-30

Study Completion Date

2014-11-30

Brief Summary

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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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Detailed Description

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Conditions

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HIV

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Web sites

Individuals assigned to this arm are given a list of websites where they can view additional information relating to condom use.

Group Type NO_INTERVENTION

No interventions assigned to this group

Condom-HIM

Individuals assigned to this arm must follow an on-line one session tailored intervention.

Group Type EXPERIMENTAL

Condom-HIM

Intervention Type 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.

Interventions

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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.

Intervention Type BEHAVIORAL

Eligibility Criteria

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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.