NCT01154309

Brief Summary

The investigators will adapt and test an existing treatment (group CBT for depression) for use in outpatient substance use treatment settings as delivered by trained substance use counselors. The investigators expect that treatment will lead to improved depression and substance use outcomes.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
73

participants targeted

Target at P50-P75 for phase_1 depression

Timeline
Completed

Started Sep 2006

Typical duration for phase_1 depression

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 1, 2006

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2009

Completed
10 months until next milestone

First Submitted

Initial submission to the registry

June 29, 2010

Completed
1 day until next milestone

First Posted

Study publicly available on registry

June 30, 2010

Completed
Last Updated

November 16, 2011

Status Verified

November 1, 2011

Enrollment Period

3 years

First QC Date

June 29, 2010

Last Update Submit

November 10, 2011

Conditions

DepressionSubstance Use

Keywords

DepressionSubstance UseGroup Cognitive Behavioral Therapy

Outcome Measures

Primary Outcomes (2)

  • Reductions in depressive symptoms as measured by the BDI II

    Post treatment

  • Reductions in AOD use

    Post treatment

Study Arms (2)

1

EXPERIMENTAL

Clients are invited to attend 18 group CBT sessions

Behavioral: Group CBT for Depression and AOD Disorders

2

NO INTERVENTION

Clients receive usual care

Interventions

Group CBT for Depression and AOD DisordersBEHAVIORAL

18 sessions of 2-hour group CBT

1

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Enrolled in outpatient substance abuse program
  • BDI II score \>13
  • Probable alcohol or substance use problem

You may not qualify if:

  • Cognitive impairment (Short Blessed \> 10)
  • Probably bipolar or schizophrenic disorder

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Behavioral Health Services, Inc

Gardena, California, 90249, United States

Location

MeSH Terms

Conditions

DepressionSubstance-Related Disorders

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorChemically-Induced DisordersMental Disorders

Study Officials

  • Katherine E Watkins, MD, MSHS

    RAND

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 29, 2010

First Posted

June 30, 2010

Study Start

September 1, 2006

Primary Completion

September 1, 2009

Study Completion

September 1, 2009

Last Updated

November 16, 2011

Record last verified: 2011-11

Locations

US(1)