Actively Recruiting

Phase Not Applicable
Age: 18Years - 25Years
All Genders
NCT06074354

Assessing the Use of MY-RIDE, a Just-in-time Adaptive Intervention, to Improve HIV Prevention and Substance Use in Youth Experiencing Homelessness

Led by The University of Texas Health Science Center, Houston · Updated on 2026-05-13

450

Participants Needed

1

Research Sites

145 weeks

Total Duration

On this page

Sponsors

T

The University of Texas Health Science Center, Houston

Lead Sponsor

N

National Institute of Nursing Research (NINR)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to determine whether Motivating Youth to Reduce Infections, Disconnections, and Emotion dysregulation (MY-RIDE) decreases substance use , to determine whether MY-RIDE increases human immunodeficiency virus (HIV) prevention strategies and to evaluate MY-RIDE effects on willingness to take Pre-Exposure Prophylaxis (PrEP), stress, substance use urge, and use of mental health and substance use services when compared to attention control youth

CONDITIONS

Official Title

Assessing the Use of MY-RIDE, a Just-in-time Adaptive Intervention, to Improve HIV Prevention and Substance Use in Youth Experiencing Homelessness

Who Can Participate

Age: 18Years - 25Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have engaged in substance use (alcohol or illicit drugs)
  • Speak English
  • Are experiencing homelessness
  • Engaged in sexual activity in the last 6 months or plan to in the next month
  • Are not planning to move out of the metro area during the 15-month study period
Not Eligible

You will not qualify if you...

  • Youth experiencing homelessness with low literacy (score less than 4 on the Rapid Estimate of Adult Literacy in Medicine-Short Form)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The University of Texas Health Science Center at Houston

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

D

Diane M Santa Maria, DrPH, MSN, RN, PHNA-BC, FSAHM

CONTACT

J

Jennifer Jones

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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