Counseling for Primary Care Office-based Buprenorphine
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT00595764 |
Recruitment Status :
Completed
First Posted : January 16, 2008
Results First Posted : October 6, 2014
Last Update Posted : April 3, 2020
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Opiate Dependence | Behavioral: Manual-guided Physician Management (PM) Behavioral: Physician Management (PM) combined with on-site manual-guided Cognitive Behavioral Therapy (CBT) | Phase 4 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 141 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Counseling for Primary Care Office-based Buprenorphine |
Study Start Date : | August 2005 |
Actual Primary Completion Date : | February 2011 |
Actual Study Completion Date : | February 2011 |

Arm | Intervention/treatment |
---|---|
Active Comparator: 1
Physician Management
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Behavioral: Manual-guided Physician Management (PM)
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. |
Experimental: 2
Physician Management plus Cognitive Behavioral Therapy
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Behavioral: Physician Management (PM) combined with on-site manual-guided Cognitive Behavioral Therapy (CBT)
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. |
- Illicit Opioid Abstinence [ Time Frame: 6 months ]number of weeks of abstinence from illicit opioids, as documented by urine toxicology and self-report. Range 0 - 24.
- Treatment Completion [ Time Frame: 6 months ]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 [ Time Frame: 6 months ]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. [ Time Frame: 6 months ]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 [ Time Frame: 6 months ]
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.

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years to 65 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
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

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00595764
United States, Connecticut | |
The APT Foundation, Inc. -- Welch Building | |
New Haven, Connecticut, United States, 06519 | |
Yale New Haven Hospital Primary Care Center | |
New Haven, Connecticut, United States, 06519 |
Principal Investigator: | David A. Fiellin, MD | Yale University |
Responsible Party: | Yale University |
ClinicalTrials.gov Identifier: | NCT00595764 |
Obsolete Identifiers: | NCT00632151 |
Other Study ID Numbers: |
0504027657 5R01DA019511 ( U.S. NIH Grant/Contract ) |
First Posted: | January 16, 2008 Key Record Dates |
Results First Posted: | October 6, 2014 |
Last Update Posted: | April 3, 2020 |
Last Verified: | April 2020 |
Buprenorphine Buprenorphine/naloxone Counseling Primary care |
Opioid-Related Disorders Narcotic-Related Disorders Substance-Related Disorders Chemically-Induced Disorders Mental Disorders |