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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06074354
Enrollment
450
Registered
2023-10-10
Start date
2024-11-11
Completion date
2027-08-23
Last updated
2026-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

Brief summary

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

Interventions

BEHAVIORALAttention-control group

Participants will receive a one-hour general health promotion session from a nurse and be issued a phone that will deploy the EMA on the same schedule as the intervention arm. They will also receive usual care from the clinics, drop-in center, and shelter recruitment sites. Usual care includes accessing social workers and case managers for immediate housing, food, and clothing needs and assistance in navigating the local Continuum of Care system to access social services.

BEHAVIORALMY-RIDE group

MY-RIDE has three main components: 1) One nurse-led face-to-face session; 2) three months of Ecological Momentary Assessments (EMA) with personalized messaging delivered by phone in real-time in response to one's current risk; and 3) access to on-demand healthcare/PrEP navigation and referrals.

Sponsors

The University of Texas Health Science Center, Houston
Lead SponsorOTHER
National Institute of Nursing Research (NINR)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* 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.

Exclusion criteria

* Youth Experiencing Homelessness (YEH) who have low literacy based on the Rapid Estimate of Adult Literacy in Medicine-Short Form (scores \< 4)

Design outcomes

Primary

MeasureTime frame
Change in substance usebaseline, end of intervention (3 months after baseline), 3 months after intervention, 6 months after intervention, and 12 months after intervention

Secondary

MeasureTime frameDescription
Change in condom usebaseline, end of intervention (3 months after baseline), 3 months after intervention, 6 months after intervention, and 12 months after intervention
Change in PrEP uptake as assessed by the self reported toolbaseline, end of intervention (3 months after baseline), 3 months after intervention, 6 months after intervention, and 12 months after interventionPrEP uptake is defined as the self initiation of HIV prevention medication
Change in sexually transmitted infections (STIs)baseline, end of intervention (3 months after baseline), 3 months after intervention, 6 months after intervention, and 12 months after interventionThis will be assessed by a blood test to detect biomarkers for HIV and Syphilis, and urine test for Gonorrhea and Chlamydia

Countries

United States

Contacts

CONTACTDiane M Santa Maria, DrPH, MSN, RN, PHNA-BC, FSAHM
Diane.M.SantaMaria@uth.tmc.edu713-500-2002
CONTACTJennifer Jones
Jennifer.D.Torres@uth.tmc.edu713-500-9928
PRINCIPAL_INVESTIGATORDiane M Santa Maria, DrPH, MSN, RN, PHNA-BC, FSAHM

The University of Texas Health Science Center, Houston

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 14, 2026