RECRUITING

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

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

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

Quick Facts

Study Start:2024-11-11
Study Completion:2025-06-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06074354

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 25 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * have engaged in substance use (alcohol or illicit drugs)
  2. * speak English
  3. * are experiencing homelessness
  4. * engaged in sexual activity in the last 6 months or plan to in the next month
  5. * are not planning to move out of the metro area during the 12-month study period.
  1. * Youth Experiencing Homelessness (YEH) who have low literacy based on the Rapid Estimate of Adult Literacy in Medicine-Short Form (scores \< 4)

Contacts and Locations

Study Contact

Diane M Santa Maria, DrPH, MSN, RN, PHNA-BC, FSAHM,
CONTACT
713-500-2002
Diane.M.SantaMaria@uth.tmc.edu
Jennifer Jones
CONTACT
713-500-9928
Jennifer.D.Torres@uth.tmc.edu

Principal Investigator

Diane M Santa Maria, DrPH, MSN, RN, PHNA-BC, FSAHM,
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center, Houston

Study Locations (Sites)

The University of Texas Health Science Center at Houston
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center, Houston

  • Diane M Santa Maria, DrPH, MSN, RN, PHNA-BC, FSAHM,, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center, Houston

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-11-11
Study Completion Date2025-06-01

Study Record Updates

Study Start Date2024-11-11
Study Completion Date2025-06-01

Terms related to this study

Additional Relevant MeSH Terms

  • HIV Infections