- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02112201
The ProGirls Study
September 14, 2020 updated by: Oregon Research Institute
Preventing HIV/STI Risk Behavior in Girls With Delinquency, Drug Abuse, & Trauma
Girls in the juvenile justice system who have high rates of delinquency, drug abuse, and trauma are particularly at risk for engaging in risky sexual behavior and for contracting HIV/AIDS or other sexually transmitted infections (STIs).
No effective prevention programs for girls who have this combination of behaviors is known to exist at this time.
Researchers are developing, assessing, and implementing a family-centered prevention program to decrease girls' participation in the risky behaviors associated with the spread of HIV and STIs.
The program also includes a group-based training and support program for parents.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study aims to test an intervention to reduce HIV/STI risk behavior among girls in the juvenile justice system with the triple-threat risk of delinquency, drug abuse, and trauma.
This is a competing continuation of the ProTeens study (Preventing Drug Abuse & HIV/AIDS in Delinquent Youths: An Integrated Intervention) which focused on testing a family-centered intervention for treating HIV risk, drug use, and delinquency in boys.
The current study will adapt the ProTeens intervention for girls.
Girls and their parent(s) will be randomly assigned to either a family-centered intervention condition (INT; n = 100) or to an active comparison condition (n = 100) consisting of group therapy and case management (GCM).
The INT condition will consist of individually administered HIV preventive intervention for adolescent girls involved in the juvenile justice system that integrally addresses delinquency, drug abuse, and trauma exposure, along with group-based training and support for parents.
The girl and parent components will run concurrently for three months.
The GCM condition will consist of group therapy and case management for girls provided as usual by the juvenile justice department.
We will examine intervention effects on proximal outcomes measured at 12 months, the effects of childhood adversity on proximal outcomes, and the mediation of intervention effects.
Longer term outcomes will be measured at 24 months.
Data will be collected through in-person interviews and questionnaires from focal participants and their parents, official arrest records, and urinary analysis.
Study Type
Interventional
Enrollment (Actual)
416
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Oregon
-
Eugene, Oregon, United States, 97403
- Oregon Research Institute
-
-
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.
Eligibility Criteria
Ages Eligible for Study
13 years to 18 years (ADULT, CHILD)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- female, age 13-18 years
- living in Lane County, Oregon
- living at home (biological/adoptive, foster, or other relative care)
- at least one criminal referral and on probation or a formal accountability contract with the juvenile justice system
- documented drug use from juvenile justice risk assessment
- traumatic exposure
- no imminent plans to be placed in out-of-home care
Exclusion Criteria:
- meet criteria for posttraumatic stress disorder
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Integrated intervention for parents and adolescent girls
Twelve session parent education and support group; twelve session one-on-one adolescent skills training intervention
|
The intervention will consist of individually administered preventive curriculum for adolescent girls involved in the juvenile justice system that integrally addresses delinquency, drug abuse, and trauma exposure, along with group-based training and support for parents.
|
|
NO_INTERVENTION: Treatment as usual
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reduction in HIV/STIs risk behavior in delinquent girls
Time Frame: Baseline and post intervention (6 mos); 12 & 24 month follow-ups
|
Girls in the intervention condition are expected to have significantly lower rates of HIV/STI risk behaviors compared to girls in the control condition at each of the time-points post-baseline.
Data will be collected through in-person interviews and questionnaires from focal participants and their parents.
|
Baseline and post intervention (6 mos); 12 & 24 month follow-ups
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reduction in criminal offending
Time Frame: Baseline and post intervention (6 mos); 12 & 24 month follow-ups
|
Girls in the intervention condition are expected to have significantly lower rates of criminal offending behavior compared to girls in the control condition at each of the time points post-baseline.
Data will be collected through in-person interviews and questionnaires from focal participants and their parents and official arrest records.
|
Baseline and post intervention (6 mos); 12 & 24 month follow-ups
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reduction in substance use
Time Frame: Baseline and post intervention (6 mos); 12 & 24 month follow-ups
|
Girls in the intervention condition are expected to have significantly lower rates of substance use compared to girls in the control condition at each of the time-points post-baseline.
Data will be collected through in-person interviews and questionnaires from focal participants and their parents and urinary analysis.
|
Baseline and post intervention (6 mos); 12 & 24 month follow-ups
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Dana K Smith, PhD, Oregon Research Institute
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 Major Dates
Study Start
September 1, 2013
Primary Completion (ACTUAL)
August 1, 2018
Study Completion (ACTUAL)
May 1, 2020
Study Registration Dates
First Submitted
April 3, 2014
First Submitted That Met QC Criteria
April 9, 2014
First Posted (ESTIMATE)
April 11, 2014
Study Record Updates
Last Update Posted (ACTUAL)
September 16, 2020
Last Update Submitted That Met QC Criteria
September 14, 2020
Last Verified
September 1, 2020
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DA025857
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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