- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00725959
Online Social Networking for HIV Prevention
November 1, 2017 updated by: Sheana Bull, Colorado School of Public Health
In this randomized controlled trial, we will identify social networks on Facebook, an randomly assign each network to control or intervention status.
We will then intervene at the level of the network with dynamic, interactive HIV prevention messages (intervention) or static messages about HIV prevention (control).
We will develop the intervention content with input from our target audience (Facebook users) and will measure baseline, and 3 and 6 month assessments of condom use and abstinence among all participants
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
1578
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years to 24 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Facebook user with an existing Facebook page
- at least 16
- no older than 24
- English speaker
Exclusion Criteria:
- older than 24 or younger than 16
- non English speaker
- does not have a Facebook page
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Facebook Arm
Participants in this arm will have exposure to innovative, dynamic and regularly updated HIV Prevention messages on Facebook
|
messages about HIV posted in online social networking sites
|
|
Active Comparator: Control arm
Participants in this arm will have exposure to static information on HIV prevention currently available online
|
messages about HIV posted in online social networking sites
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Proportion of Condom Usage
Time Frame: two months
|
number of times condom used divided by number of times person had sex in past 60 days
|
two months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Condom and Abstinence Norms, Attitudes, Self-efficacy and Intentions
Time Frame: two months
|
two months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Sheana Bull, Ph.D., University of Colorado at Denver and Health Sciences
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2008
Primary Completion (Actual)
December 1, 2010
Study Completion (Actual)
December 1, 2011
Study Registration Dates
First Submitted
July 29, 2008
First Submitted That Met QC Criteria
July 29, 2008
First Posted (Estimate)
July 31, 2008
Study Record Updates
Last Update Posted (Actual)
November 7, 2017
Last Update Submitted That Met QC Criteria
November 1, 2017
Last Verified
October 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- COMIRB 07-0459
- R01NR010492 (U.S. NIH Grant/Contract)
- 1R01NR01492-01
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.