Facilitating Implementation of Cognitive Behavioral Therapy in Primary Care and Community Clinics
1 other identifier
interventional
23
1 country
1
Brief Summary
The investigators propose to test the effect of external facilitation on the extent that brief cognitive behavioral therapy (CBT) for depression is incorporated into routine practice in primary care and community based clinics in the VA. The investigators will provide training in brief CBT to mental health providers in participating clinics. To the investigators' knowledge, this will be the first study of the effect of external facilitation on outcomes of a training intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable depression
Started May 2008
Longer than P75 for not_applicable depression
1 active site
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
May 1, 2008
CompletedFirst Submitted
Initial submission to the registry
May 9, 2008
CompletedFirst Posted
Study publicly available on registry
May 13, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2015
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2015
CompletedSeptember 23, 2015
September 1, 2015
7.3 years
May 9, 2008
September 21, 2015
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
CBT progress notes
Monthly post-training for 6 months
Study Arms (1)
Facilitation
EXPERIMENTALTherapists receive assistance with adopting CBT
Interventions
Study facilitator meets regularly with therapists to aid implementation of CBT
Eligibility Criteria
You may qualify if:
- mental health clinicians in selected clinics who do or are willing to do psychotherapy.
You may not qualify if:
- clinicians who do not do psychotherapy in eligible clinics.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Michael E. DeBakey VA Medical Center
Houston, Texas, 77030, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Michael R Kauth, PhD
South Central MIRECC
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Intervention Model
- PARALLEL
- Sponsor Type
- FED
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Director for Education, SC MIRECC
Study Record Dates
First Submitted
May 9, 2008
First Posted
May 13, 2008
Study Start
May 1, 2008
Primary Completion
September 1, 2015
Study Completion
September 1, 2015
Last Updated
September 23, 2015
Record last verified: 2015-09