Actively Recruiting

Phase Not Applicable
Age: 14Years - 19Years
FEMALE
NCT05368571

CHOICES-TEEN Randomized Controlled Trial

Led by University of Texas at Austin · Updated on 2025-06-19

400

Participants Needed

1

Research Sites

209 weeks

Total Duration

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Sponsors

U

University of Texas at Austin

Lead Sponsor

W

Wayne State University

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

CHOICES-TEEN Randomized Controlled Trial

Who Can Participate

Age: 14Years - 19Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Female adolescents aged 14 to 19 years
  • At risk of substance-exposed pregnancy and HIV/STI
  • Report sexual intercourse with a male in the last 3 months
  • Report inconsistent or ineffective condom use in the last 3 months
  • Report inconsistent or ineffective contraception use in the last 3 months
Not Eligible

You will not qualify if you...

  • Severe cognitive or psychiatric impairment preventing cooperation with study protocol
  • Do not speak or read/write in English
  • Unable to meet study requirements, including follow-up assessments

AI-Screening

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Trial Site Locations

Total: 1 location

1

Baylor University

Houston, Texas, United States, 77002

Actively Recruiting

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Research Team

D

Danielle E Parrish, Ph.D.

CONTACT

K

Kirk L von Sternberg, Ph.D.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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