- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02424643
Improving Survey Procedures for Young Men Who Have Sex With Men in Web-based HIV Prevention: Retention Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Men who have sex with men (MSM) are the risk population most heavily impacted by HIV in the United States by any measure; in 2009, at least 61% of new HIV infections were estimated to have occurred in MSM. MSM are experiencing an increase in HIV transmission that has been occurring since at least 1990, and accelerated in multiple North American and European countries from 2000-2005. The expansion of the HIV epidemic has been proposed to be attributable, in part, to the extent to which the internet has facilitated sexual connectivity among MSM.
Researchers have attempted to reach MSM for HIV prevention research and intervention on the internet. In the past 10 years, there has been a proliferation of internet surveys and HIV research studies among men who have sex with men that utilize the internet for data collection and, in some cases, the delivery of HIV prevention content. The development of internet-based interventions has been recently identified as especially promising because of its potential for scalability. However, there are also important limitations to internet-based data collections and prevention studies. The most important of these relate to representativeness and opportunities to introduce bias to data collections and differences in access to and use of internet among different subgroups of MSM. Equally important, although less discussed, are the unique ethical and human research protections challenges posed by online sexual health prevention studies.
The investigators will conduct an experiment to improve knowledge of how to conduct internet-based HIV prevention research with MSM in ways that decrease biases in data collections. The design will consist of a randomized controlled trials of MSM recruited online. A total of 1000 MSM will be enrolled to determine how to best improve retention in online surveys.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Georgia
-
Atlanta, Georgia, United States, 30322
- Rollins School of Public Health, Emory University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- male
- aged 18 to 34 years
- have had sex with another man in the past 12 months
Exclusion Criteria:
- female or transgender
- younger than 18 years of age
- older than 34 years of age
- have not had sex with another man in the past 12 months.
Study Plan
How is the study designed?
Design Details
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: No Incentive
Participants in this arm will receive no compensation for taking the online survey.
|
|
Experimental: Monetary Incentive
Participants in this arm will receive a $20 Amazon.com
incentive for participating in the online survey.
|
$20 Amazon.com gift card
|
Experimental: Altruistic Incentive
Participants in this arm will receive altruistic messages throughout the length of the survey in hopes of improving survey completion.
|
A preliminary statement of the importance of participation, and periodic "inspirational" messages throughout the length of the survey emphasizing the value to men's health by completing the survey
|
Experimental: Dashboard Incentive
Participants in this arm will receive a dashboard at the end of the survey that will compare their data entered into the survey to other participants who have taken the survey.
A preview of this dashboard will be shown at the beginning of the survey as a teaser in the hopes to improve survey completion.
|
A sample "dashboard" will compare data subjects enter in their survey to the data already collected from other men who have taken the survey.
For the dashboard, men who complete the survey will be shown how their own reported data about certain topics compared to other men's data.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Proportion of survey completed before dropping out.
Time Frame: At baseline survey
|
We expect that the average participant will complete 40 screens of survey in about 45 minutes.
Based on historical data, about 75% of participants will complete all screens.
Analyses will take a time-to-event approach and hazard of discontinuing survey will be calculated.
|
At baseline survey
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IRB00065333a
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.
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