Cognitive Behavioral Treatment of Posttraumatic Stress Disorder Enhanced by Virtual Reality for Individuals With PTSD and Substance Abuse

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Joann Difede, Weill Medical College of Cornell University
ClinicalTrials.gov Identifier:
NCT00656344
First received: April 7, 2008
Last updated: December 6, 2013
Last verified: December 2013

April 7, 2008
December 6, 2013
October 2006
December 2013   (final data collection date for primary outcome measure)
posttraumatic stress symptomatology [ Time Frame: prior to treatment, during the treatment, immediately following treatment and 6 months after the completion of treatment ] [ Designated as safety issue: No ]
posttraumatic stress symptomatology [ Time Frame: prior to treatment, immediately following treatment and 6 months after the completion of treatment ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00656344 on ClinicalTrials.gov Archive Site
substance use symptomatology [ Time Frame: prior to treatment, during treatment, immediately following treatment, and 6 months after the completion of treatment ] [ Designated as safety issue: No ]
substance use symptomatology [ Time Frame: prior to treatment, immediately following treatment, and 6 months after the completion of treatment ] [ Designated as safety issue: No ]
Not Provided
Not Provided
 
Cognitive Behavioral Treatment of Posttraumatic Stress Disorder Enhanced by Virtual Reality for Individuals With PTSD and Substance Abuse
Cognitive Behavioral Treatment of Posttraumatic Stress Disorder Enhanced by Virtual Reality for Individuals With PTSD and Substance Abuse

This study is exploring the use of an intervention designed to treat PTSD in individuals with comorbid PTSD and substance abuse resulting from the attacks of September 11 or from military service in Iraq. A cognitive behavioral treatment protocol will be used to treat PTSD. The exposure component of the protocol will be enhanced with the use of virtual reality in which the client will view a virtual environment while describing their trauma.

Not Provided
Interventional
Not Provided
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Posttraumatic Stress Disorder
  • Substance Abuse
Other: Cognitive behavioral treatment enhanced by virtual reality
A cognitive behavioral protocol with cognitive and behavioral techniques will be used to treat symptoms. The exposure part of the treatment will be enhanced with the use of a virtual environment.
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
3
December 2013
December 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • English-speaking
  • Between the ages of 18 and 70
  • Exposed to the WTC Attacks (were in towers or in the immediate area) or veterans of the Iraq War
  • Diagnosed with PTSD symptoms
  • Current substance abuse disorder or history of substance abuse disorder

Exclusion Criteria:

  • Presence of current organic mental disorder
  • Presence or history of schizophrenia, bipolar disorder or depression with psychotic features, delusional disorder
  • Active suicidal ideation, intent, or plan
  • Active homicidal ideation, intent, or plan
  • Use of pacemaker
  • Medically unstable
  • History of seizures
Both
18 Years to 70 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00656344
9603000551
Yes
Joann Difede, Weill Medical College of Cornell University
Weill Medical College of Cornell University
Not Provided
Principal Investigator: JoAnn Difede Weill Medical College of Cornell University
Weill Medical College of Cornell University
December 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP