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Clinical Trials/NCT01162044
NCT01162044UnknownNot Applicable

Interrupting Traumatic Memories: An Emergency Room Intervention for the Prevention of PTSD

Hadassah Medical Organization1 site in 1 country80 target enrollmentStarted: November 1, 2010Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Enrollment
80
Locations
1
Primary Endpoint
PTSD symptoms

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
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.

Arms & Interventions

No intervention

No Intervention

Subjects will be assessed, but no active intervention given

Computer game

Experimental

Subjects will play with computer game while in the Emergency Room

Intervention: Computer game (Other)

Outcomes

Primary Outcomes

PTSD symptoms

Time Frame: 6 months

PTSD status and symptoms as measured by the PSS

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other

Study Sites (1)

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