Completed

Improving Survey Procedures for Young Men Who Have Sex With Men in Web-based HIV Prevention: Retention Study

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What is being tested

Monetary Incentive

+ Altruistic Incentive

+ Dashboard Incentive

Behavioral
Who is being recruted

From 18 to 34 Years
+7 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Interventional
Study Start: April 2015
See protocol details

Summary

Principal SponsorEmory University
Last updated: January 27, 2026
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Study start date: April 1, 2015

Actual date on which the first participant was enrolled.

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.

Official TitleImproving Survey Procedures for Young Men Who Have Sex With Men in Web-based HIV Prevention: Retention Study
NCT02424643
Principal SponsorEmory University
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

1131 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Criteria

Male

Biological sex of participants that are eligible to enroll.

From 18 to 34 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Criteria

3 inclusion criteria required to participate
male

aged 18 to 34 years

have had sex with another man in the past 12 months

4 exclusion criteria prevent from participating
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

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

3 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Participants in this arm will receive a $20 Amazon.com incentive for participating in the online survey.

Group II

Experimental
Participants in this arm will receive altruistic messages throughout the length of the survey in hopes of improving survey completion.

Group III

Experimental
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.

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Rollins School of Public Health, Emory University

Atlanta, United StatesOpen Rollins School of Public Health, Emory University in Google Maps
CompletedOne Study Center