search
Back to results

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

Primary Purpose

Opioid Use Disorder

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
12 Week Manualized Cognitive-Behavioral Therapy Intervention
Sponsored by
Philadelphia College of Osteopathic Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opioid Use Disorder

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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")

Sites / Locations

  • Prevention Point PhiladelphiaRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

12 Week Manualized Cognitive-Behavioral Therapy Intervention

Arm Description

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

Outcomes

Primary Outcome Measures

Urinalysis-confirmed Reduction or Elimination of Illicit Opioid Use

Secondary Outcome Measures

The Patient Health Questionnaire-9 (PHQ-9)
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.
The Brief Assessment of Recovery Capital (BARC-10)
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).
The Client Satisfaction Questionnaire-8 (CSQ-8)
The CSQ-8 is a brief, eight-item treatment satisfaction questionnaire.

Full Information

First Posted
August 17, 2023
Last Updated
August 17, 2023
Sponsor
Philadelphia College of Osteopathic Medicine
Collaborators
Prevention Point Philadelphia
search

1. Study Identification

Unique Protocol Identification Number
NCT06008769
Brief Title
Cognitive-Behavioral Therapy for Opioid Use Disorder: A Manualized Pilot Study
Official Title
Cognitive-Behavioral Therapy for Opioid Use Disorder: A Manualized Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 6, 2023 (Actual)
Primary Completion Date
May 2024 (Anticipated)
Study Completion Date
August 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Philadelphia College of Osteopathic Medicine
Collaborators
Prevention Point Philadelphia

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. 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.
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opioid Use Disorder

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
12 Week Manualized Cognitive-Behavioral Therapy Intervention
Arm Type
Experimental
Arm Description
Participants will receive a once-per-week, 12 week manualized cognitive-behavioral therapy intervention.
Intervention Type
Behavioral
Intervention Name(s)
12 Week Manualized Cognitive-Behavioral Therapy Intervention
Intervention Description
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.
Primary Outcome Measure Information:
Title
Urinalysis-confirmed Reduction or Elimination of Illicit Opioid Use
Time Frame
Baseline, 12 weeks
Secondary Outcome Measure Information:
Title
The Patient Health Questionnaire-9 (PHQ-9)
Description
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.
Time Frame
Baseline, 12 weeks
Title
The Brief Assessment of Recovery Capital (BARC-10)
Description
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).
Time Frame
Baseline, 12 weeks
Title
The Client Satisfaction Questionnaire-8 (CSQ-8)
Description
The CSQ-8 is a brief, eight-item treatment satisfaction questionnaire.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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")
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michelle R Lent, PhD
Phone
2158716138
Email
michellele@pcom.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Hannah R Callahan, MPH
Phone
2158716628
Email
hannahca@pcom.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michelle R Lent, PhD
Organizational Affiliation
Philadelphia College of Osteopathic Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prevention Point Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19134
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Denise Botcheos, LCSW
Phone
215-285-1999
Email
deniseb@ppponline.org
First Name & Middle Initial & Last Name & Degree
Chad Gurdgiel, MSW, LSW
Email
chadgurdgiel@ppponline.org

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26406300
Citation
Kampman K, Jarvis M. American Society of Addiction Medicine (ASAM) National Practice Guideline for the Use of Medications in the Treatment of Addiction Involving Opioid Use. J Addict Med. 2015 Sep-Oct;9(5):358-67. doi: 10.1097/ADM.0000000000000166.
Results Reference
background
PubMed Identifier
22514846
Citation
Center for Substance Abuse Treatment. Clinical Guidelines for the Use of Buprenorphine in the Treatment of Opioid Addiction. Rockville (MD): Substance Abuse and Mental Health Services Administration (US); 2004. Report No.: (SMA) 04-3939. Available from http://www.ncbi.nlm.nih.gov/books/NBK64245/
Results Reference
background
PubMed Identifier
23762965
Citation
Guidelines for the Psychosocially Assisted Pharmacological Treatment of Opioid Dependence. Geneva: World Health Organization; 2009. Available from http://www.ncbi.nlm.nih.gov/books/NBK143185/
Results Reference
background
PubMed Identifier
26808307
Citation
Dugosh K, Abraham A, Seymour B, McLoyd K, Chalk M, Festinger D. A Systematic Review on the Use of Psychosocial Interventions in Conjunction With Medications for the Treatment of Opioid Addiction. J Addict Med. 2016 Mar-Apr;10(2):93-103. doi: 10.1097/ADM.0000000000000193.
Results Reference
background
PubMed Identifier
29596405
Citation
Seth P, Scholl L, Rudd RA, Bacon S. Overdose Deaths Involving Opioids, Cocaine, and Psychostimulants - United States, 2015-2016. MMWR Morb Mortal Wkly Rep. 2018 Mar 30;67(12):349-358. doi: 10.15585/mmwr.mm6712a1.
Results Reference
background
PubMed Identifier
20599130
Citation
McHugh RK, Hearon BA, Otto MW. Cognitive behavioral therapy for substance use disorders. Psychiatr Clin North Am. 2010 Sep;33(3):511-25. doi: 10.1016/j.psc.2010.04.012.
Results Reference
background
Citation
Substance Abuse and Mental Health Services Administration. Behavioral health treatments and services; 2017. Retrieved from https://www.samhsa.gov/treatment. Accessed September 6. 2018.
Results Reference
background
Citation
Beck AT. Cognitive therapy: nature and relation to behavior therapy. Behav Ther. 1970;1(2),184-200.
Results Reference
background
Citation
Ellis A. Reason and Emotion in Psychotherapy. New York, NY: Stuart; 1962.
Results Reference
background
Citation
Festinger DS, Lent MR. Cognitive-Behavioral Therapy (CBT) for the Treatment of Opioid Use Disorder. Trafford Publishing; 2022 Aug 18.
Results Reference
background
PubMed Identifier
33971028
Citation
Lent MR, Callahan HR, Womer P, Mullen PM, Shook CB, DiTomasso RA, Felgoise SH, Festinger DS. A mental health professional survey of cognitive-behavioral therapy for the treatment of opioid use disorder. J Clin Psychol. 2021 Jul;77(7):1607-1613. doi: 10.1002/jclp.23170. Epub 2021 May 10.
Results Reference
background
PubMed Identifier
22614936
Citation
Moore BA, Barry DT, Sullivan LE, O'connor PG, Cutter CJ, Schottenfeld RS, Fiellin DA. Counseling and directly observed medication for primary care buprenorphine maintenance: a pilot study. J Addict Med. 2012 Sep;6(3):205-11. doi: 10.1097/ADM.0b013e3182596492.
Results Reference
background
PubMed Identifier
23260506
Citation
Fiellin DA, Barry DT, Sullivan LE, Cutter CJ, Moore BA, O'Connor PG, Schottenfeld RS. A randomized trial of cognitive behavioral therapy in primary care-based buprenorphine. Am J Med. 2013 Jan;126(1):74.e11-7. doi: 10.1016/j.amjmed.2012.07.005.
Results Reference
background
PubMed Identifier
23734858
Citation
Ling W, Hillhouse M, Ang A, Jenkins J, Fahey J. Comparison of behavioral treatment conditions in buprenorphine maintenance. Addiction. 2013 Oct;108(10):1788-98. doi: 10.1111/add.12266. Epub 2013 Jul 12.
Results Reference
background
PubMed Identifier
11556941
Citation
Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med. 2001 Sep;16(9):606-13. doi: 10.1046/j.1525-1497.2001.016009606.x.
Results Reference
background
PubMed Identifier
17874169
Citation
Gilbody S, Richards D, Brealey S, Hewitt C. Screening for depression in medical settings with the Patient Health Questionnaire (PHQ): a diagnostic meta-analysis. J Gen Intern Med. 2007 Nov;22(11):1596-602. doi: 10.1007/s11606-007-0333-y. Epub 2007 Sep 14.
Results Reference
background
PubMed Identifier
28578224
Citation
Vilsaint CL, Kelly JF, Bergman BG, Groshkova T, Best D, White W. Development and validation of a Brief Assessment of Recovery Capital (BARC-10) for alcohol and drug use disorder. Drug Alcohol Depend. 2017 Aug 1;177:71-76. doi: 10.1016/j.drugalcdep.2017.03.022. Epub 2017 May 19.
Results Reference
background

Learn more about this trial

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

We'll reach out to this number within 24 hrs