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Counseling for Primary Care Office-based Buprenorphine

Primary Purpose

Opiate Dependence

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Manual-guided Physician Management (PM)
Physician Management (PM) combined with on-site manual-guided Cognitive Behavioral Therapy (CBT)
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Opiate Dependence focused on measuring Buprenorphine, Buprenorphine/naloxone, Counseling, Primary care

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • opioid dependence

Exclusion Criteria:

  • current dependence on alcohol, cocaine, benzodiazepines or sedatives
  • current suicide or homicide risk
  • current psychotic disorder or untreated major depression
  • inability to read or understand English
  • life-threatening or unstable medical problems

Sites / Locations

  • The APT Foundation, Inc. -- Welch Building
  • Yale New Haven Hospital Primary Care Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

1

2

Arm Description

Physician Management

Physician Management plus Cognitive Behavioral Therapy

Outcomes

Primary Outcome Measures

Illicit Opioid Abstinence
number of weeks of abstinence from illicit opioids, as documented by urine toxicology and self-report. Range 0 - 24.

Secondary Outcome Measures

Treatment Completion
The number of patients who completed the study (did not meet the criteria for protective transfer baseed on drug use, did not miss medication for more than seven days, or did not miss three or more Physician Management sessions) at 24 weeks.
Cocaine Abstinence
Total weeks of cocaine abstinence as documented by weekly urine toxicology analysis. Range from 0 to 24.
Criminal Activity- Addiction Severity Index (ASI) Legal Composite Score.
The ASI Legal Composite score ranges from 0 to 1 with higher scores corresponding to greater legal problems.
Overall Health- Short Form (36) Health Survey
Short Form (36) Health Survey overall score ranges from 0 to 100. Computed as the mean of all SF-36 subscales. The SF-36 is a multi-purpose, short-form health survey with only 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index. Lower scores are greater disability and higher scores are greater health functioning.

Full Information

First Posted
October 3, 2007
Last Updated
April 1, 2020
Sponsor
Yale University
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT00595764
Brief Title
Counseling for Primary Care Office-based Buprenorphine
Official Title
Counseling for Primary Care Office-based Buprenorphine
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
August 2005 (undefined)
Primary Completion Date
February 2011 (Actual)
Study Completion Date
February 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Yale University
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The major goal is to determine whether adding cognitive behavioral therapy to physician management will increase the efficacy of buprenorphine/naloxone treatment in an office-based primary care setting.
Detailed Description
To evaluate the need for drug counseling aimed at reducing illicit drug use and increasing buprenorphine/naloxone adherence, the proposed study compares manual-guided Physician Management (PM) and PM combined with on-site manual-guided Cognitive Behavioral Therapy (CBT) in a 24 week randomized clinical trial of buprenorphine/naloxone in a heterogeneous population of opioid dependent patients (N=140) in a primary care clinic. PM, consistent with federal regulations, is designed to reflect usual care by primary care physicians and includes referral to ancillary services. CBT will be provided by skilled psychologists in weekly sessions for the first 12 weeks and focuses on reducing illicit drug use and increasing buprenorphine/naloxone adherence. The study will test the hypothesis that that the addition of CBT to PM will lead to decreased illicit drug use, durable effects after counseling has been discontinued, improved buprenorphine/naloxone adherence and will demonstrate incremental cost-effectiveness in patients receiving buprenorphine/naloxone maintenance in primary care. Primary outcome measures include reductions in illicit opioid use and abstinence achievement, as assessed by weekly urine toxicology testing and self report. Secondary outcome measures include retention in treatment, reductions in cocaine use and HIV risk, decreased criminal activity and improved health and employment status. Utilization and costs of services, spillover effects in the PCC, and patient and staff perceptions of benefits and problems associated with primary care agonist maintenance treatment will also be evaluated. The results of this study will help define the role of professional evidence-based drug counseling in expanding access to treatment with buprenorphine/naloxone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Opiate Dependence
Keywords
Buprenorphine, Buprenorphine/naloxone, Counseling, Primary care

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
141 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Active Comparator
Arm Description
Physician Management
Arm Title
2
Arm Type
Experimental
Arm Description
Physician Management plus Cognitive Behavioral Therapy
Intervention Type
Behavioral
Intervention Name(s)
Manual-guided Physician Management (PM)
Intervention Description
Manual-guided Physician Management (PM) PM, consistent with federal regulations, is designed to reflect usual care by primary care physicians and includes referral to ancillary services.
Intervention Type
Behavioral
Intervention Name(s)
Physician Management (PM) combined with on-site manual-guided Cognitive Behavioral Therapy (CBT)
Intervention Description
CBT is provided by skilled psychologists in weekly sessions for the first 12 weeks and focuses on reducing illicit drug use and increasing Buprenorphine adherence.
Primary Outcome Measure Information:
Title
Illicit Opioid Abstinence
Description
number of weeks of abstinence from illicit opioids, as documented by urine toxicology and self-report. Range 0 - 24.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Treatment Completion
Description
The number of patients who completed the study (did not meet the criteria for protective transfer baseed on drug use, did not miss medication for more than seven days, or did not miss three or more Physician Management sessions) at 24 weeks.
Time Frame
6 months
Title
Cocaine Abstinence
Description
Total weeks of cocaine abstinence as documented by weekly urine toxicology analysis. Range from 0 to 24.
Time Frame
6 months
Title
Criminal Activity- Addiction Severity Index (ASI) Legal Composite Score.
Description
The ASI Legal Composite score ranges from 0 to 1 with higher scores corresponding to greater legal problems.
Time Frame
6 months
Title
Overall Health- Short Form (36) Health Survey
Description
Short Form (36) Health Survey overall score ranges from 0 to 100. Computed as the mean of all SF-36 subscales. The SF-36 is a multi-purpose, short-form health survey with only 36 questions. It yields an 8-scale profile of functional health and well-being scores as well as psychometrically-based physical and mental health summary measures and a preference-based health utility index. Lower scores are greater disability and higher scores are greater health functioning.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: opioid dependence Exclusion Criteria: current dependence on alcohol, cocaine, benzodiazepines or sedatives current suicide or homicide risk current psychotic disorder or untreated major depression inability to read or understand English life-threatening or unstable medical problems
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David A. Fiellin, MD
Organizational Affiliation
Yale University
Official's Role
Principal Investigator
Facility Information:
Facility Name
The APT Foundation, Inc. -- Welch Building
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06519
Country
United States
Facility Name
Yale New Haven Hospital Primary Care Center
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06519
Country
United States

12. IPD Sharing Statement

Citations:
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
result

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Counseling for Primary Care Office-based Buprenorphine

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