CClinicalTrials.gg
Status unknownNCT01162044Updated Jul 14, 2010

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

An interventional study of Computer game in Posttraumatic Stress Disorder, sponsored by Hadassah Medical Organization. Status unknown at 1 site in Israel. Open to participants aged 18 Years to 65 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2010-07-14.

Sponsored by Hadassah Medical Organization · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Jul 2010), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Study 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.

02

Conditions studied

  • Posttraumatic Stress Disorder

Keywords

  • PTSD
  • prevention
03

In context

Emergencies

1,694 studies on the registry are indexed under Emergencies; 332 are open to participants now.

This study's planned enrollment of 80 is below the median of 145 across 932 interventional studies indexed under Emergencies.

Browse Emergencies studies →

Lead sponsor

Hadassah Medical Organization is the lead sponsor of 660 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
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

Exclusion Criteria:

  • current or past psychiatric treatment,
  • current or past PTSD.
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
80 participants (estimated)

Study arms

  • 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

Interventions

  • OtherComputer game

    Playing with specially designed computer game while in emergency room

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What researchers measure

Primary outcomes

  1. PTSD symptoms

    PTSD status and symptoms as measured by the PSS

    Time frame: 6 months

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Study locations

1 site
  • Hadassah Medical Center
    Jerusalem, Israel
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 14, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01162044
Lead sponsor
Hadassah Medical Organization
First posted
Jul 14, 2010
Start date
Nov 2010
Primary completion
Jun 2011 (estimated)
Completion
Sep 2011 (estimated)
Last update
Jul 14, 2010

Study contacts

Sara A Freedman, PhD
Contact
sarafreedman@gmail.com
972544704636
Rena Cooper, MD
principal investigator · Hadassah Medical Organization

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2010. You cannot join it, but the record below documents what was studied.

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