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Mobile Messaging Intervention to Present New HIV Prevention Options for Men Who Have Sex With Men (MSM) — MMI4MSM RCT  

Human Immunodeficiency Virus Clinical Trial

Official title:
Mobile Messaging Intervention to Present New HIV Prevention Options for MSM - Randomized Controlled Trial

Clinical Trial Summary

The study will evaluate the use and effectiveness of mobile-messaging platforms as a public health strategy for improving sexual health outcome measures among men who have sex with men (MSM) by determining whether exposure to the message-delivery platform results in improvements in participants' self-reported sexual health and prevention behaviors, beliefs and attitudes. The study will enroll men into a randomized controlled trial. Participants randomized to the messaging intervention will have access to a smartphone-based messaging platform for three months while those assigned to the waitlist group will be offered access to the messaging platform after all follow up is complete. Participants will complete surveys at baseline, after the end of the 3 month intervention, and follow up surveys 6 and 9 months after the baseline survey.

Clinical Trial Description

This study aims to evaluate the use and effectiveness of a smartphone-based messaging platform as a public health strategy for improving participants' self-reported sexual health and prevention behaviors, beliefs and attitudes. The study will enroll 1,206 men into a randomized controlled trial. They will be assigned to either the immediate intervention group ("intervention arm") or the waitlist-control group ("waitlist-control arm"). All participants will take an assessment survey at baseline, and the intervention group will be oriented on the installation and use of the messaging app upon randomization to that group. All men in the randomized controlled trial will complete short follow-up surveys at 3-month intervals during the 9-month follow-up period. When the intervention arm activities and assessments have concluded, participants in the waitlist-control arm will then be given the option of accessing to the intervention app and participation in intervention post-test activities. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03666247
Study type Interventional
Source Emory University
Contact
Status Completed
Phase N/A
Start date January 24, 2018
Completion date December 18, 2019
View Details
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