Trial of Art Therapy During Cognitive Processing Therapy for PTSD
NCT ID: NCT02610049
Last Updated: 2017-08-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
31 participants
INTERVENTIONAL
2013-11-30
2017-02-13
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Control
Subjects will receive 8 sessions of Cognitive Processing Therapy.
Cognitive Processing therapy
8 sessions of standard CPT from CPT manual developed by Dr. S Resick, Monson \& Chard (11/2010)
Experimental
Subjects will receive 8 sessions of CPT + Art Therapy 8 sessions of individual therapy.
Art + CPT
8 sessions of individual therapy of mixes techniques Art + CPT 8 sessions of standard CPT (same 8 as in control group) from manual developed by Dr.s Resick, Monson \& Chard (11/2010)
Experimental 2
Subject to receive 8 sessions of individual therapy for Art + CPT Cognitive Processing Therapy intervention pre-specified to be administered separately.
CPT + Art Therapy
Subjects to complete 8 sessions of standard Cognitive Processing Therapy from manual developed by Dr. S. Resick, Monson \& Chard (1/2010) CPT + Art Therapy of mixed individual techniques
Interventions
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Cognitive Processing therapy
8 sessions of standard CPT from CPT manual developed by Dr. S Resick, Monson \& Chard (11/2010)
Art + CPT
8 sessions of individual therapy of mixes techniques Art + CPT 8 sessions of standard CPT (same 8 as in control group) from manual developed by Dr.s Resick, Monson \& Chard (11/2010)
CPT + Art Therapy
Subjects to complete 8 sessions of standard Cognitive Processing Therapy from manual developed by Dr. S. Resick, Monson \& Chard (1/2010) CPT + Art Therapy of mixed individual techniques
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Both genders,
* All ethnicities,
* Veterans in treatment for PTSD,
Exclusion Criteria
* No active suicidal or homicidal ideation,
* No psychosis
18 Years
ALL
No
Sponsors
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Hampton VA Medical Center
FED
Responsible Party
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Principal Investigators
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Barbara Cross, Ph.D., FNP
Role: STUDY_CHAIR
IRB Chair
Locations
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Hampton VA Medical Center
Hampton, Virginia, United States
Countries
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Other Identifiers
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13-04
Identifier Type: -
Identifier Source: org_study_id
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