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Clinical Trials/NCT03308097
NCT03308097CompletedNot Applicable

A Mobile Intervention to Improve Uptake of PrEP for Southern Black MSM

Rhode Island Hospital2 sites in 1 country70 target enrollmentStarted: November 20, 2018Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
70
Locations
2
Primary Endpoint
Number of PrEP Services Appointments Attended-Full Sample

Study Overview

Brief Summary

This study will develop and test an interactive mobile messaging intervention to improve engagement in care related to Pre-exposure Prophylaxis (PrEP) and decrease HIV risk behaviors for Black men who have sex with men living in the Southern U.S. The mobile messaging intervention will include interactive text messaging and free, publicly available links to websites and YouTube videos. During the intervention participants will gain information about their health, improve motivation for engagement in PrEP related care, and build skills for healthy behaviors. Participants will also receive intervention materials to help decrease frequent barriers to care. If the intervention is found to be effective, it can be tested in a larger study and then disseminated.

Detailed Description

The uptake of Pre-Exposure Prophylaxis (PrEP) has been slow for young Black men who have sex with men (BMSM) living in the Southern United States. This is a significant issue because eight of the ten states with the highest rates of new HIV infections are located in the South. Jackson, Mississippi (MS) (the site of this project) has the second highest AIDS diagnosis rate in the nation, and the highest rate of HIV infection for young urban Black men who have sex with men. This study will develop and test an engaging, interactive, and cost effective mobile messaging intervention to improve linkage to PrEP care for BMSM (18-35 yrs) living in Jackson, MS. BMSM eligible for PrEP, receiving care at the University of Mississippi Medical Center sexually-transmitted infections (STI)/HIV testing clinics, will be texted interactive links to publicly available, online content about PrEP and HIV prevention. Links will be sent to PrEP eligible BMSM by 8-16 interactive text messages over 4 weeks. The material used in the intervention will be consistent with the Information Motivation Behavior (IMB) Model and will address cultural and structural barriers to initiating PrEP care. A small randomized controlled study among 66 new participants in the clinics will examine the preliminary efficacy of the intervention compared to enhanced standard of care on attendance at a PrEP Services Appointment (the first step in initiating PrEP care). It is hypothesized that, compared to BMSM receiving enhanced standard of care, BMSM receiving the PrEP Mobile Messaging Intervention will show greater attendance at a PrEP Services Appointment and decreased HIV risk behavior at 4 and 16 weeks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 35 Years (Adult)
Sex
Male
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • English speaking
  • Black MSM
  • Eligible for PrEP
  • Visit STI/HIV testing clinics at University of Mississippi Medical Center
  • Able to give consent/assent and not impaired by cognitive or medical limitations as per clinical assessment

Exclusion Criteria

  • Involved in another PrEP or HIV prevention related study

Outcomes

Primary Outcomes

Number of PrEP Services Appointments Attended-Full Sample

Time Frame: 16 weeks

With participant consent, staff at the STI/HIV testing clinic will abstract from the electronic medical record any PrEP Services Appointment, and any PrEP related care.

Number of Participants Who Received a PrEP Prescription-Restricted Sample

Time Frame: 16 weeks

Staff at the testing clinic will abstract any prescription written for PrEP at 16 weeks for the participant. Restricted sample is those who did not receive a PrEP prescription the same day as enrollment.

Number of PrEP Services Appointments Attended- Restricted Sample

Time Frame: 16 weeks

With participant consent, staff at the STI/HIV testing clinic will abstract from the electronic medical record any PrEP Services Appointment, and any PrEP related care. Restricted Sample is only those who did not receive a PrEP prescription the same day as enrollment.

Number of Participants Who Received a PrEP Prescription-Full Sample

Time Frame: 16 weeks

Staff at the testing clinic will abstract any prescription written for PrEP at 16 weeks for the participant.

Secondary Outcomes

  • Change in PrEP Knowledge-Restricted Sample(Baseline, 16 weeks)
  • Change in Social Motivational Readiness for PrEP Care-Full Sample(Baseline, 16 weeks)
  • Change in Social Motivational Readiness for PrEP Care-Restricted Sample(Baseline, 16 weeks)
  • Change in PrEP Self-efficacy-Full Sample(Baseline, 16 weeks)
  • Change in PrEP Self-efficacy-Restricted Sample(Baseline, 16 weeks)
  • Change in PrEP Knowledge-Full Sample(Baseline, 16 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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