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Behavioral Intervention
Contingency Management + Coaching for Substance Use Disorders (PEERS Trial)
N/A
Recruiting
Research Sponsored by Chestnut Health Systems
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline to 30 months
Awards & highlights
No Placebo-Only Group
Summary
This trial looks at how coaches with lived experience can help young adults access and use evidence-based substance use practices.
Who is the study for?
This trial is for two groups: paraprofessional coaches aged 18-30 without life-threatening conditions, and emerging adult clients aged 18-26 on parole or probation with substance use disorders. Clients must have a stable address and not qualify for federal disability that would interfere with coaching.
What is being tested?
The study tests Contingency Management (CM) combined with vocational/educational coaching to reduce drug use in young adults involved in the justice system. It focuses on how well non-professional coaches can help these individuals engage in treatment.
What are the potential side effects?
Since this trial involves behavioral interventions rather than medications, traditional side effects are not applicable. However, participants may experience stress or emotional discomfort when discussing substance use and lifestyle changes.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ post-training, an average of one month, to post-service delivery of two more clients, an average of one year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~post-training, an average of one month, to post-service delivery of two more clients, an average of one year
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Changes from baseline to 6 months post-baseline in Emerging Adult Client Urine Drug Screens (measured at 0, 4, and 6 months).
Changes from baseline up to 30 months post-baseline in Paraprofessional Coach Urine Drug Screens (measured at 0, 6, 12, 18, 24, and 30 months).
Secondary study objectives
Attitudes at 6 months post-baseline in Emerging Adult Client Attitudes Toward the Services Provided (measured at 6 months).
Changes from Baseline scores compared to up to 30 months post-baseline in Paraprofessional Coach Contingency Management (CM) Adherence (measured monthly for 30 months).
Changes from baseline to 6 months in Emerging Adult Client Session Attendance and Vocational/Educational Activity Completion (measured at 1, 2, 3, 4, 5, and 6 months).
+24 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: CM combined with Vocational/educational Coaching from Coaches without Lived ExperienceExperimental Treatment1 Intervention
This group will receive contingency management (CM) combined with vocational/educational coaching from paraprofessional coaches without lived experience in community settings.
Group II: CM combined with Vocational/educational Coaching from Coaches with Lived ExperienceActive Control1 Intervention
This group will receive contingency management (CM) combined with vocational/educational coaching from paraprofessional coaches with lived experience in community settings.
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Who is running the clinical trial?
Chestnut Health SystemsLead Sponsor
23 Previous Clinical Trials
23,520 Total Patients Enrolled
Oregon Social Learning CenterLead Sponsor
35 Previous Clinical Trials
10,695 Total Patients Enrolled
National Institute on Drug Abuse (NIDA)NIH
2,582 Previous Clinical Trials
3,326,960 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- I receive federal disability benefits that prevent me from participating in educational or vocational coaching.I am between 18 and 26 years old.I am between 18 and 30 years old.I do not have any life-threatening conditions needing immediate treatment.
Research Study Groups:
This trial has the following groups:- Group 1: CM combined with Vocational/educational Coaching from Coaches with Lived Experience
- Group 2: CM combined with Vocational/educational Coaching from Coaches without Lived Experience
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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