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

NCT ID: NCT01162044

Last Updated: 2010-07-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-11-30

Study Completion Date

2011-09-30

Brief Summary

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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.

Detailed Description

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Conditions

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Posttraumatic Stress Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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No intervention

Subjects will be assessed, but no active intervention given

Group Type NO_INTERVENTION

No interventions assigned to this group

Computer game

Subjects will play with computer game while in the Emergency Room

Group Type EXPERIMENTAL

Computer game

Intervention Type OTHER

Playing with specially designed computer game while in emergency room

Interventions

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Computer game

Playing with specially designed computer game while in emergency room

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hadassah Medical Organization

OTHER

Sponsor Role lead

Responsible Party

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Hadassah Medical Center

Principal Investigators

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Rena Cooper, MD

Role: PRINCIPAL_INVESTIGATOR

Hadassah Medical Organization

Locations

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Hadassah Medical Center

Jerusalem, , Israel

Site Status

Countries

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Israel

Central Contacts

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Sara A Freedman, PhD

Role: CONTACT

972544704636

Other Identifiers

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ER-PTSD-HMO-CTIL

Identifier Type: -

Identifier Source: org_study_id

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