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Clinical Trials/NCT00229307
NCT00229307CompletedNot Applicable

Prolonged Exposure (PE) Treatment for Post Traumatic Stress Disorder (PTSD) 20 Minutes Versus 40 Minutes

Sheba Medical Center2 sites in 1 country39 target enrollmentStarted: December 2005Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
39
Locations
2
Primary Endpoint
PSS-i
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

Comparing the efficacy of 40 minutes PE treatment to 20 minutes of the same treatment

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • •Psychotic symptoms
  • •Dissociation
  • •Drug or Alcohol dependence

Outcomes

Primary Outcomes

PSS-i

Time Frame: 15 weeks and 1-year follow-up

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other Gov
Responsible Party
Sponsor

Study Sites (2)

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Prolonged Exposure (PE) Treatment for Post... | Clinical Trial