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Examining an Emergency Room Intervention for the Prevention of Post Traumatic Stress Disorder (PTSD)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01162044
Recruitment Status : Unknown
Verified July 2010 by Hadassah Medical Organization.
Recruitment status was:  Not yet recruiting
First Posted : July 14, 2010
Last Update Posted : July 14, 2010
Information provided by:
Hadassah Medical Organization

Brief Summary:
PTSD is a common and distressing possible outcome following exposure to a traumatic event. Recent studies show that memory processes may be central to the development of the disorder, and interrupting the consolidation of traumatic memories may prevent the disorder from developing. Specifically the use of a visual spatial task has been shown to reduce a key characteristic of PTSD, intrusions, in non-clinical populations. This study aims to administer a visual spatial task to recent trauma survivors in the Emergency Room, and compare PTSD and symptoms development in these patients as compared to a control group who did not carry out the task. The study hypothesizes that the task will result in less PTSD, lower levels of intrusions, dissociation and pain.

Condition or disease Intervention/treatment
Posttraumatic Stress Disorder Other: Computer game

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 80 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Prevention
Official Title: Interrupting Traumatic Memories: An Emergency Room Intervention for the Prevention of PTSD
Study Start Date : November 2010
Estimated Primary Completion Date : June 2011
Estimated Study Completion Date : September 2011

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Arm Intervention/treatment
No Intervention: No intervention
Subjects will be assessed, but no active intervention given
Experimental: Computer game
Subjects will play with computer game while in the Emergency Room
Other: Computer game
Playing with specially designed computer game while in emergency room

Primary Outcome Measures :
  1. PTSD symptoms [ Time Frame: 6 months ]
    PTSD status and symptoms as measured by the PSS

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 65 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

  • age 18-65,
  • no loss of consciousness,
  • ability to understand study procedures and give informed consent,
  • Hebrew as first language,
  • experienced a potentially traumatic event as defined in DSM (objective danger and subjective feeling of fear).

Exclusion Criteria:

  • current or past psychiatric treatment,
  • current or past PTSD.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01162044

Contact: Sara A Freedman, PhD 972544704636

Hadassah Medical Center Not yet recruiting
Jerusalem, Israel
Sponsors and Collaborators
Hadassah Medical Organization
Principal Investigator: Rena Cooper, MD Hadassah Medical Organization

Responsible Party: Dr Rena Cooper,, Hadassah Medical Center Identifier: NCT01162044     History of Changes
Other Study ID Numbers: ER-PTSD-HMO-CTIL
First Posted: July 14, 2010    Key Record Dates
Last Update Posted: July 14, 2010
Last Verified: July 2010

Keywords provided by Hadassah Medical Organization:

Additional relevant MeSH terms:
Stress Disorders, Traumatic
Stress Disorders, Post-Traumatic
Disease Attributes
Pathologic Processes
Trauma and Stressor Related Disorders
Mental Disorders