Cognitive-Behavioral Therapy for Opioid Use Disorder: A Manualized Pilot Study

Sponsor
Philadelphia College of Osteopathic Medicine (Other)
Overall Status
Recruiting
CT.gov ID
NCT06008769
Collaborator
Prevention Point Philadelphia (Other)
20
1
1
11.9
1.7

Study Details

Study Description

Brief Summary

The goal of this pilot clinical trial is to test the feasibility of a 12-week manualized cognitive-behavioral therapy treatment for opioid use disorder in reducing or stopping illicit opioid use in a community setting. Participants will complete 12 weeks of therapy with a behavioral health counselor and will complete assessments at baseline and 12 weeks. Other outcomes include changes in mood and perceptions of recovery-related support after 12 weeks of therapy.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: 12 Week Manualized Cognitive-Behavioral Therapy Intervention
N/A

Detailed Description

Cognitive-Behavioral Therapy (CBT) is one of the most well-supported and widely used psychosocial treatments for substance use disorders (SUDs); however, few studies have evaluated the efficacy of CBT for opioid use disorder (OUD). This prospective, longitudinal pilot study (pre-post design) will assess the feasibility of the first manualized CBT treatment for OUD in adults (N = 20) in a community-based setting (Prevention Point Philadelphia). This study will utilize clinical (urinalysis), patient-reported, and provider-reported outcomes (mood, support, feasibility, satisfaction with treatment) over 12 weeks of a manualized cognitive-behavioral treatment for OUD. This prospective, longitudinal pilot study will evaluate the feasibility of a novel psychotherapy for OUD. This study will utilize both clinical (urinalysis) and patient or provider-reported (mood, support, feasibility) outcomes to assess the feasibility of 12 weeks of manualized cognitive-behavioral treatment for OUD. All study recruitment, consent and intervention delivery will occur at Prevention Point (2913-15 Kensington Ave, Philadelphia, PA). Outcomes will include participant-reported treatment satisfaction, as well as EMR-extracted clinical data (session attendance, urinalysis, mood, demographics, medical information, and recovery-related support).

We hypothesize that individuals with OUD will demonstrate a reduction illicit opioid use from baseline to week 12 as assessed by urinalysis (% change, positive/negative). As a secondary outcome, use of other substances will also be assessed from baseline to week 12 (e.g., alcohol, cocaine). Use of medication for OUD (MOUD; e.g., buprenorphine. methadone) will be accounted for in analyses.

We hypothesize that mood and perceptions of recovery-related resources will improve from baseline to week 12.

As an exploratory aim, we will evaluate intervention feasibility through electronic medical record (EMR) data of number of sessions attended over 12 weeks, treatment fidelity checklists, and a participant survey of treatment satisfaction.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Cognitive-Behavioral Therapy for Opioid Use Disorder: A Manualized Pilot Study
Actual Study Start Date :
Aug 6, 2023
Anticipated Primary Completion Date :
May 1, 2024
Anticipated Study Completion Date :
Aug 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: 12 Week Manualized Cognitive-Behavioral Therapy Intervention

Participants will receive a once-per-week, 12 week manualized cognitive-behavioral therapy intervention.

Behavioral: 12 Week Manualized Cognitive-Behavioral Therapy Intervention
The manualized intervention, Cognitive Behavioral Therapy for Opioid Use Disorder, was co-written and developed by the study PI, Dr. Lent (see Appendix). The manual consists of one module (Module 0) on assessment and 12 modules of CBT. This study will focus on delivery of Modules 1-12 that focus on several tenets of CBT, including skill development (cognitive restructuring, refusal skills, problem-solving, coping strategies), functional analysis (triggers, reinforcement) and utilizing the cognitive model.

Outcome Measures

Primary Outcome Measures

  1. Urinalysis-confirmed Reduction or Elimination of Illicit Opioid Use [Baseline, 12 weeks]

Secondary Outcome Measures

  1. The Patient Health Questionnaire-9 (PHQ-9) [Baseline, 12 weeks]

    The PHQ-9 is a nine-item instrument (0-3 Likert type scale) for monitoring and measuring depression severity over the past two weeks. The PHQ-9 has strong validity and reliability and is frequently used in clinical settings.

  2. The Brief Assessment of Recovery Capital (BARC-10) [Baseline, 12 weeks]

    The BARC-10 is a 10-item measure assessing the perceived characteristics and assets and individual develops on their recovery journey. The BARC-10 has high internal consistency (α = .90).

  3. The Client Satisfaction Questionnaire-8 (CSQ-8) [12 weeks]

    The CSQ-8 is a brief, eight-item treatment satisfaction questionnaire.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patient at Prevention Point Philadelphia

  • 18 years or older

  • Living with opioid use disorder

  • Has a goal to reduce or eliminate illicit opioid use

  • Able to provide informed consent

Exclusion Criteria:
  • Not comfortable receiving psychotherapy in English

  • Under custodial supervision through the legal justice system (e.g., halfway house following incarceration, involuntary detention or confinement, status as a "prisoner")

Contacts and Locations

Locations

Site City State Country Postal Code
1 Prevention Point Philadelphia Philadelphia Pennsylvania United States 19134

Sponsors and Collaborators

  • Philadelphia College of Osteopathic Medicine
  • Prevention Point Philadelphia

Investigators

  • Principal Investigator: Michelle R Lent, PhD, Philadelphia College of Osteopathic Medicine

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Philadelphia College of Osteopathic Medicine
ClinicalTrials.gov Identifier:
NCT06008769
Other Study ID Numbers:
  • H23-025
First Posted:
Aug 24, 2023
Last Update Posted:
Aug 24, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 24, 2023