Accelerated Resolution Therapy (ART) for Psychological Trauma
- Conditions
- Psychological TraumaPTSD
- Interventions
- Behavioral: Accelerated Resolution Therapy (ART)Behavioral: Waitlist
- Registration Number
- NCT01559688
- Lead Sponsor
- University of South Florida
- Brief Summary
Service members and veterans often experience symptoms of psychological trauma following combat deployments. While efforts are being made in the military and at the Veteran's Affairs to meet the large number of soldiers and veterans experiencing symptoms of psychological trauma, there remains a need to evaluate new treatments, particularly those that are designed to be brief in length.
A new therapy, known as Accelerated Resolution Therapy (ART), is a type of psychological therapy that is designed for rapid resolution of symptoms of psychological trauma. This approach uses a combination of talking and sets of eye movements guided by the therapist. During therapy, this interactive personal guidance is thought to be helpful in resolving problems (such as bad memories).
The purpose of this study is to:
1. Evaluate how effective ART is in treating symptoms of psychological trauma among non-active duty veterans who served in Operation Iraqi Freedom and Operation Enduring Freedom in Iraq and in Afghanistan or other combat conflicts.
2. Learn if there is improvement in symptoms of psychological trauma (such as bad memories, anxiety, depression, and guilt) after receiving Accelerated Resolution Therapy (ART).
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 63
- Non-active duty U.S. veteran of any prior deployment(s) with recruitment emphasis on those who previously served in Iraq and/or Afghanistan (OIF and OEF).
- At least 18 years of age.
- Symptoms indicative of psychological trauma. This includes a score of >40 on the PCL-M Checklist, or in the absence of a score >40, therapist assessment of symptoms of PTSD, as determined from the Checklist for Accelerated Resolution Therapy (ART) Standard Protocol. Individuals with previous treatment for psychological trauma, yet with residual symptoms, will be eligible.
- Ability to read and speak English to complete survey questions.
- Denial of suicidal ideation or intent, including homicidal ideation or intent, and no evidence of psychotic behavior or being in psychological crisis
- Brain injury prohibiting speech, writing, and purposeful actions
- Identified to have current suicidal ideation
- Major psychiatric disorder concomitant to symptoms of psychological trauma
- Currently undergoing substance abuse treatment
- Previous diagnosis of eye movement disorder
- Any medical condition that, in the judgment of the Principal Investigator and/or ART therapist, may place the individual at high risk due to a potential heightened emotional reaction
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description ART therapy group Accelerated Resolution Therapy (ART) Participants in this arm will receive 2-5 sessions of ART therapy, depending on individual progress. Each session will last 60-90 minutes over a 2-week period. Waitlist Waitlist Participants in this group will receive 2 fitness assessment or career counseling sessions. Each session will last 60-90 minutes over a 2-week period. Upon completion of this arm, participants will be offered the choice to start ART therapy.
- Primary Outcome Measures
Name Time Method Change in PTSD Checklist (PCL-M) score from baseline to end of treatment approximately 2 weeks This questionnaire asks about symptoms in response to "stressful military experiences."
- Secondary Outcome Measures
Name Time Method Change in sleep quality as measured by the Pittsburgh Sleep Quality Index (PSQI) from baseline to endpoint approximately 2 weeks Change in psychological wellness as measured by Brief Symptom Inventory from baseline to endpoint approximately 2 weeks Change in trauma-related guilt as measured by Trauma-Related Guilt Inventory from baseline to endpoint approximately 2 weeks Change in depressive symptoms as measured by the Center for Epidemiologic Depression (CES-D) scale from baseline to endpoint approximately 2 weeks Change in anxiety symptoms as measured by State-Trait Inventory from baseline to endpoint approximately 2 weeks Change in self-compassion scale score from baseline to endpoint approximately 2 weeks Change in anger as measured by Aggression Questionnaire from baseline to endpoint approximately 2 weeks
Trial Locations
- Locations (1)
University of South Florida
🇺🇸Tampa, Florida, United States