NCT05368571 CHOICES-TEEN Randomized Controlled Trial
| NCT ID | NCT05368571 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Texas at Austin |
| Condition | Risk for an Alcohol-Exposed Pregnancy |
| Study Type | INTERVENTIONAL |
| Enrollment | 400 participants |
| Start Date | 2022-04-08 |
| Primary Completion | 2026-04-10 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 400 participants in total. It began in 2022-04-08 with a primary completion date of 2026-04-10.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
This randomized controlled trial will: 1) Test the efficacy of the CHOICES-TEEN (CT) intervention compared with an Attentional Control (AC) condition on reducing the risk of substance-exposed pregnancy (SEP) and HIV/STI among high-risk female youth involved with the juvenile justice system by reducing alcohol use, increasing marijuana cessation, reducing risk of pregnancy, and increasing condom use; 2) Test the efficacy of CT, compared to AC, on increasing cognitive self-regulation abilities; 3) Test proposed intervention mediators/mechanisms of action for CT overall and by race/ethnicity; and 4) Test the moderating effect of initial readiness to change on risk of SEP and risk of HIV/STI.
Eligibility Criteria
Inclusion Criteria: Female adolescents between 14-19 years of age, of any race, who are at risk of substance-exposed pregnancy and HIV/STI will be eligible. Specifically, they must report the following behaviors within the last 3 months: * sexual intercourse with a male * inconsistent/ineffective condom use AND * inconsistent/ineffective contraception use Exclusion Criteria: * severe cognitive and/or psychiatric impairment that precludes cooperation with study protocol, per judgement of the interventionist or research staff * do not speak or read/write in English * unable to meet study requirements, including follow-up assessments
Contact & Investigator
Danielle E Parrish, Ph.D.
PRINCIPAL INVESTIGATOR
Baylor University
Frequently Asked Questions
Who can join the NCT05368571 clinical trial?
This trial is open to female participants only, aged 14 Years or older, up to 19 Years, studying Risk for an Alcohol-Exposed Pregnancy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT05368571 currently recruiting?
Yes, NCT05368571 is actively recruiting participants. Contact the research team at danielle_parrish@baylor.edu for enrollment information.
Where is the NCT05368571 trial being conducted?
This trial is being conducted at Houston, United States.
Who is sponsoring the NCT05368571 clinical trial?
NCT05368571 is sponsored by University of Texas at Austin. The principal investigator is Danielle E Parrish, Ph.D. at Baylor University. The trial plans to enroll 400 participants.