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Psychotherapy Treatment of Deployment-Related PTSD in Primary Care Settings

Psychotherapy Treatment of Deployment-related PTSD in Primary Care Settings

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00974402
Enrollment
35
Registered
2009-09-10
Start date
2008-03-31
Completion date
2012-06-30
Last updated
2014-09-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Combat Disorders, Post-Traumatic Stress Disorders, Stress Disorders

Keywords

Active duty, Afghanistan, Anger, Anxiety, Avoidance, BAMC, Brooke Army Medical Center, Cognitive Behavioral Therapy, Combat, Combat Disorder, Coping, Counseling, Counselor, Deployment, Depression, Exposure, Fear, Feeling alone, Flashbacks, Guard, Guilt, Hospitalization, Iraq, Mental Health, Military, Military member, Military personnel, Neuroses, Nightmares, OEF, OIF, Prolonged Exposure Therapy, Psychiatric, Psychiatric medication, Psychological distress, Psychotherapy, Reserve, Retired, Sadness, Separated, Sleeplessness, Soldier, Stress, Stress disorder, Stress management, STRONG STAR, Suicidal, Suicide, Therapy, Trauma, Traumatic Event, Trouble Sleeping, Veteran, Veterans, War, WHMC, Wilford Hall Medical Center, PTSD, Posttraumatic Stress Disorders

Brief summary

The purpose of this study is to evaluate Cognitive-behavioral therapy (CBT) for deployment-related post-traumatic stress disorder (PTSD) that can be used by behavioral health consultants working with Service Members in the primary care clinic. CBT is a well-researched, very effective individual (one-to-one) treatment that is designed to help people to directly deal with traumatic events they have suffered in the past, including combat. Many Service Members prefer to see behavioral health providers in primary care rather than the mental health clinic. The researchers hope to learn if a brief treatment for PTSD in primary care can be just as useful as more traditional treatment given in the mental health clinic. This study will enroll approximately 45 participants overall; with approximately 30 participants at Wilford Hall Medical Center or Brooke Army Medical Center, and 15 participants to be enrolled at the South Texas Veterans Health Care System over a period of one year.

Interventions

BEHAVIORALCognitive Behavioral Therapy

The study investigators have developed a 4-session PTSD treatment plan including a behavioral health consultants (BHC) manual and a patient guide for use in primary care. Therapists will be psychologists who are functioning as behavioral health consultants (BHC) in an integrated primary care clinic. The study will adapt intervention methods for use in the time-constrained primary care environment from Cognitive Behavioral Therapy(ies) that have proven effective for PTSD in specialty mental health care settings. Study participants will receive four 30-minute treatment sessions over six weeks.

Sponsors

Brooke Army Medical Center
CollaboratorFED
59th Medical Wing
CollaboratorFED
South Texas Veterans Health Care System
CollaboratorFED
The University of Texas Health Science Center at San Antonio
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* The target population for the study is active duty, reserve, guard, separated, or retired OIF/OEF veterans (minimum age 18 and English speaking) in the primary care population who are symptomatic for deployment-related PTSD and interested in treatment. * Symptomatic for PTSD will be defined as a minimum score of 32 on the PTSD CheckList - Military (PCL-M).

Exclusion criteria

* The

Design outcomes

Primary

MeasureTime frameDescription
PTSD symptomatologyBaseline, post-treatment, 6-month and 12-monthPTSD symptoms as assessed by an evaluator-administered interview (PTSD Symptom Scale Interview - PSSI) and self-report form (PTSD Checklist - Military Version - PCL-M).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026