Stress Disorders, Post-Traumatic Clinical Trial
— STRIVEOfficial title:
Suicide and Trauma Reduction Initiative Among VEterans
NCT number | NCT03933059 |
Other study ID # | 300841 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | March 21, 2019 |
Est. completion date | December 31, 2022 |
Verified date | May 2023 |
Source | University of Utah |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The present study is a pragmatic clinical trial that will examine the effectiveness of Cognitive Processing Therapy (CPT) in reducing PTSD symptom severity, depression symptoms, and suicidal thoughts among military personnel and veterans with PTSD when delivered in three different formats: (1)12 sessions delivered once per week in an office/clinic setting; (2) 12 sessions delivered once per day in an office/clinic setting; and (3) 12 sessions delivered once per day in a recreational setting.
Status | Completed |
Enrollment | 45 |
Est. completion date | December 31, 2022 |
Est. primary completion date | December 31, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. 18 years of age or older; 2. Current or prior service in the U.S. military; 3. Currently meet criteria for a diagnosis of posttraumatic stress disorder (as determined by the CAPS-5); 4. Be able to complete the informed consent process. Exclusion Criteria: 1. Current substance dependence disorder; 2. Severe suicide ideation during the past two weeks (as determined by the BSSI and clinical interview) warranting hospitalization; 3. Suicide attempt during the previous three months; 4. Impaired mental status that precludes ability to provide informed consent (e.g., intoxication, psychosis, mania). |
Country | Name | City | State |
---|---|---|---|
United States | University of Utah | Salt Lake City | Utah |
Lead Sponsor | Collaborator |
---|---|
University of Utah | The Boeing Company |
United States,
Bryan CJ, Leifker FR, Rozek DC, Bryan AO, Reynolds ML, Oakey DN, Roberge E. Examining the effectiveness of an intensive, 2-week treatment program for military personnel and veterans with PTSD: Results of a pilot, open-label, prospective cohort trial. J Clin Psychol. 2018 Dec;74(12):2070-2081. doi: 10.1002/jclp.22651. Epub 2018 Jun 19. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in PTSD symptom severity since baseline measured by the Clinician Administered PTSD Scale | Interviewer administered measure to determine the severity of PTSD. Items are summed to create a total score (Range: 0-80) where higher scores indicate greater symptom severity. | Past month symptoms, assessed within a month of completing treatment, and 6-months, 12-months, 18-months, and 24 months after completing treatment | |
Primary | Change in PTSD symptom severity since baseline measured by the Clinician Administered PTSD Scale | Interviewer administered measure to determine the severity of PTSD. Items are summed to create a total score (Range: 0-80) where higher scores indicate greater symptom severity. | Past week symptoms, assessed the last day of treatment for those completing the two week treatment retreats | |
Secondary | Change in suicidal thoughts and behaviors since baseline measured by the Scale for Suicidal Ideation | Self-report assessment of severity of suicidal thoughts and behaviors. Items are summed (range: 0-63) and higher scores indicate greater suicide severity. | Past week symptoms, assessed within a month of completing treatment, and 6-months, 12-months, 18-months, and 24 months after completing treatment | |
Secondary | Change in depression symptom severity since baseline measured by the Patient Health Questionnaire | Self-report assessment of depression symptom severity. Items are summed (range: 0-27) and higher scores indicate greater depression symptom severity. | Past two week symptoms, assessed within a month of completing treatment, and 6-months, 12-months, 18-months, and 24 months after completing treatment |
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