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Effectiveness of Trauma Management Therapy and Prolonged Exposure Therapy

Not Applicable
Completed
Conditions
PTSD
Registration Number
NCT04549493
Lead Sponsor
University of Central Florida
Brief Summary

The purpose of this requirement is to identify an effective exposure psychotherapy paradigm for the treatment of Post-Traumatic Stress Disorder (PTSD) in active duty service members and veterans by comparing different exposure psychotherapy modalities. The long-term goal of exposure psychotherapy is to improve the mental health of U.S. service members and veterans with military-related PTSD. Recovery from PTSD will reduce the economic burden not only for those persons experiencing PTSD, but also for the health care system and society as a whole (Galovski \& Lyons, 2004).

Detailed Description

This study will provide an evaluation of performance and suitability of the compressed versions of exposure psychotherapy to support the capability gap for the treatment of active duty service members and veterans with PTSD by comparing different exposure psychotherapy modalities. The overall objective of this study is to determine if compressed psychotherapy can be used as an effective alternative treatment for PTSD and to compare the impact of TMT and PE on social, familial, and occupational impairment. The primary objectives will be to compare 1) 3 week TMT with 12 week PE and 2) 3 week TMT with 2 week PE for the effectiveness of reducing PTSD symptoms in a gated approach or some other method to control for multiplicity. Outcomes will be determined based upon self-report, clinician ratings, as well as other aspects of psychopathology, and social/emotional functioning. The addition of the TMT group component will be assessed in particular to determine its impact on social, familial, and occupational impairment. Blood samples should be collected from participants at baseline and at the end of the treatment period in order to identify PTSD biomarkers, e.g. predictors of response, biological subtypes of PTSD, and therapeutic markers. Collection, storage, and transfer of the blood samples to DoD should be performed according to standardized protocols provided by the DoD. One or more site visits may occur in order to assess adherence to standardized protocols.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
134
Inclusion Criteria
  • Active duty military personnel with a diagnoses of PTSD
  • Traumatic event must have occurred during military service
  • Military sexual trauma limited to attempted or completed sexual assault.
Exclusion Criteria
  • Acute cardiac difficulties
  • Severe comorbid substance use disorders.
  • Diagnosis of schizophrenia or other psychotic disorders
  • Diagnosis of antisocial personality disorder
  • Moderate or severe traumatic brain injury (TBI)
  • Use of benzodiazepines

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Change from Baseline on the Clinician-Administered PTSD Scale for DSM-56 months posttreatment

PTSD symptoms rating scale (severity and frequency) administered by blinded clinician

Secondary Outcome Measures
NameTimeMethod
Change from Baseline on the Traumatic Life Events Questionnaire (TLEQ)6 months posttreatment

self-report measure assessing lifetime history of 22 traumatic events

Change from Baseline on the Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5)6 months posttreatment

Patient Self Report of PTSD symptoms

Sleep actigraphy - change from baseline in total sleep time6 months posttreatment

Objective assessment of sleep

Sleep actigraphy - change from baseline in sleep efficiency6 months posttreatment

Objective assessment of sleep (% of time in bed spent sleeping)

Change from Baseline on the Posttraumatic Cognitions Inventory (PTCI)6 months posttreatment

36-item measure assessing 3 domains of trauma-related cognitions (Negative Cognitions about Self, Negative Cognitions about the World, and Self-Blame)

Change from baseline on the World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0)6 months posttreatment

patient report of impairment in six domains: cognition, mobility, self-care, getting along with people, life activities (at home and work), and participation in society

Change from baseline on the Generalized Anxiety Disorder-7 (GAD-7)6 months posttreatment

Patient report measure of general anxiety symptoms

Change from Baseline on the Trauma-Related Guilt Inventory (TRGI)6 months posttreatment

32-item measure rating 3 domains of trauma-related guilt cognitions (Global Guilt, Distress, and Guilt Cognitions)

Change from Baseline on the Moral Injury Event Scale (MIES)6 months posttreatment

patient-report measure assessing psychological distress associated with violations of moral standards.

Change from baseline on the Quality of Life Scale (QOLS)6 months posttreatment

Patient report of 6 domains of life: independence, recreation, personal development and fulfillment, material and physical well-being, relationships with others, and community and civic involvement

Change from baseline on the Connor-Davidson Resilience Scale (CD-RISC)6 months posttreatment

Patient report of coping ability

Change from baseline on the Clinical Global Impressions Scales (CGI)6 months posttreatment

Clinician rated scales to evaluate the severity of pretreatment psychopathology and treatment change

Sleep actigraphy - change from baseline in wake minutes after sleep onset6 months posttreatment

Objective assessment of sleep (# of minutes awake after falling asleep)

Change from baseline on the Patient Health Questionnaire-9 (PHQ-9)6 months posttreatment

Patient report measure of depression symptoms

Change from baseline on the Dimensions of Anger Reactions-5 (DAR-5)6 months posttreatment

Patient report measure of anger

Sleep actigraphy - change from baseline in sleep onset latency6 months posttreatment

Objective assessment of sleep (# of minutes to sleep onset after getting into bed)

Trial Locations

Locations (1)

UCF RESTORES, University of Central Florida

🇺🇸

Orlando, Florida, United States

UCF RESTORES, University of Central Florida
🇺🇸Orlando, Florida, United States

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