Clinical Trials Logo

Clinical Trial Summary

Posttraumatic stress disorder (PTSD) is a condition that involves intense memories of a traumatic event and intense, persistent feelings of anxiety. There are several effective therapies for PTSD, but they are often time consuming. The investigators want to see if the investigators can shorten treatment time while keeping therapy effective by adding a medication called methylene blue, USP, taken orally as a pill, to the therapy. The specific aims are: 1) To see whether medication plus psychotherapy improves PTSD symptoms more than placebo plus psychotherapy or a waitlist; 2) To examine the long-term outcome of those receiving medication plus psychotherapy 1 and 3 months after treatment has ended; 3) To examine whether medication plus psychotherapy helps with depression, trauma-related cognitions, and functioning.


Clinical Trial Description

The psychotherapy the investigators are offering in this study is a type of cognitive behavioral therapy called imaginal exposure. In imaginal exposure, the investigators encourage the client to approach the memory of the trauma by recounting the trauma story to the therapist and discussing his or her reactions to the memory. ;


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01188694
Study type Interventional
Source University of Washington
Contact
Status Completed
Phase Phase 2
Start date September 2009
Completion date April 2013

See also
  Status Clinical Trial Phase
Completed NCT01024140 - Open Trial of Escitalopram Treatment for Male Subjects With Posttraumatic Stress Disorder N/A
Terminated NCT01574118 - Enhancing Exposure Therapy for Post-traumatic Stress Disorder Phase 2
Completed NCT00329992 - Brief Eclectic Psychotherapy for PTSD - a Randomized Controlled Trial Phase 3