- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06003725
Cultural Adaptation of Drug Treatment for DJJ Youth (CAST)
The Cultural Adaptation of an Alcohol and Other Drug Use Treatment for Black Justice Involved Youth
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Brittany E Bryant, DSW
- Phone Number: 843-973-0867
- Email: brittany.bryant@ucsf.edu
Study Locations
-
-
California
-
San Francisco, California, United States, 94110
- Recruiting
- University of California, San Francisco
-
Contact:
- Brittany Bryant, DSW
- Phone Number: 843-973-0867
- Email: brittany.bryant@ucsf.edu
-
-
South Carolina
-
Charleston, South Carolina, United States, 29425
- Completed
- Medical University of South Carolina
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
For Focus Groups and Interviews:
Black JIY Participants:
Inclusion Criteria:
• 1) Between the ages of 13-17; 2) identify as Black or African American; and 3) on community probation.
Exclusion Criteria:
• Will be excluded if they do not have parental consent to participate.
For Focus Groups and Interviews:
Adult Participants
Inclusion Criteria:
- A guardian of JIY
- An advocate (someone who supports change and reform in the justice community) for Black JIY.
Exclusion Criteria:
• Will be excluded if they do not provide consent to participate.
For pilot feasibility study:
Black JIY Participants:
Inclusion Criteria:
- Between the ages of 13 and 17
- Identify as Black or African American
- Be on community probation
- Meet criteria for alcohol, cannabis, or other drug misuse as defined by the DSM 5
- Be experiencing at least 1 problem related to AOD;
- The frequency of AOD must be weekly use over a 3-month period
Exclusion Criteria:
- Will be excluded if they do not have parental consent to participate
- Parole violation
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: ADAP-ITT Phase 8
Phase 8 consists of piloting the culturally adapted CYT intervention with 30 Black JIY to examine feasibility and acceptability.
|
The Cannabis Youth Treatment Series (CYT) (MET/CBT12 model) aims to reduce alcohol and cannabis use.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility and Acceptability
Time Frame: After study completion, an average of 3 months
|
Participants will complete feasibility and acceptability questionnaires and provide qualitative data on likes and dislikes about the intervention, delivery, session structure, and content.
|
After study completion, an average of 3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in substance use
Time Frame: Baseline, after each study visit, at study completion, up to 3 months post-intervention, an average of 6 months.
|
Participants will complete urinalysis
|
Baseline, after each study visit, at study completion, up to 3 months post-intervention, an average of 6 months.
|
|
Change in discrimination distress
Time Frame: baseline, after study completion, and up to 3 months post-intervention, an average of 6 months.
|
Participants will complete a discrimination distress assessment measure
|
baseline, after study completion, and up to 3 months post-intervention, an average of 6 months.
|
|
Change in mental health symptoms
Time Frame: Baseline, after each study visit, at study completion, up to 3 months post-intervention, an average of 6 months.
|
Participants will complete measures and questionnaires to monitor anxiety, depression, and trauma symptoms
|
Baseline, after each study visit, at study completion, up to 3 months post-intervention, an average of 6 months.
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Brittany Bryant, DSW, University of California, San Francisco
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 23-40126
- K23DA057412 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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