Integrated Intervention for Substance Abusers With Depressive Disorders
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ClinicalTrials.gov Identifier: NCT00018655 |
Recruitment Status :
Terminated
(PI has been contacted numerous times for an update, with no response. ORD requested a close out of this project. 10/2011)
First Posted : July 5, 2001
Last Update Posted : December 10, 2014
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Condition or disease | Intervention/treatment | Phase |
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Substance-Related Disorders Depressive Disorder | Behavioral: Twelve Step Facilitation Behavioral: Integrated Cognitive Behavioral Treatment | Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 276 participants |
Allocation: | Randomized |
Intervention Model: | Factorial Assignment |
Masking: | Single (Outcomes Assessor) |
Primary Purpose: | Treatment |
Official Title: | Integrated Intervention for Substance Abusers With Depressive Disorders |
Study Start Date : | April 2000 |
Actual Primary Completion Date : | September 2009 |
Actual Study Completion Date : | September 2012 |

Arm | Intervention/treatment |
---|---|
Experimental: Arm 1
Twelve Step Facilitation
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Behavioral: Twelve Step Facilitation
Twelve Step Facilitation Therapy involves focusing on topics from 12-Step programs which support sobriety goals and personal growth. |
Experimental: Arm 2
Integrated Cognitive Behavioral Treatment
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Behavioral: Integrated Cognitive Behavioral Treatment
Integrated Cognitive Behavioral Treatment involves focusing on thoughts, activities, and interactions with people related to depressive symptoms and/or substance use. |
- Hamilton Depression Scale, Timeline Follow-back (substance measure) [ Time Frame: 18 months ]

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Veterans age 18 and older with alcohol, cannabinol, and/or stimulant dependence and independent mood disorders will be included.
Exclusion Criteria:
Psychotic disorders

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): NCT00018655
United States, California | |
VA San Diego Healthcare System, San Diego | |
San Diego, California, United States, 92161 |
Principal Investigator: | Susan Tate, PhD | VA San Diego Healthcare System, San Diego |
Publications of Results:
Other Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | US Department of Veterans Affairs |
ClinicalTrials.gov Identifier: | NCT00018655 History of Changes |
Other Study ID Numbers: |
MHBS-041-99S |
First Posted: | July 5, 2001 Key Record Dates |
Last Update Posted: | December 10, 2014 |
Last Verified: | December 2014 |
Keywords provided by VA Office of Research and Development ( US Department of Veterans Affairs ):
Mood Disorders Substance-Related Disorders |
Additional relevant MeSH terms:
Disease Depressive Disorder Depression Substance-Related Disorders Pathologic Processes |
Mood Disorders Mental Disorders Behavioral Symptoms Chemically-Induced Disorders |