NCT00229307

Brief Summary

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

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
39

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2005

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 28, 2005

Completed
1 day until next milestone

First Posted

Study publicly available on registry

September 29, 2005

Completed
2 months until next milestone

Study Start

First participant enrolled

December 1, 2005

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2010

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2010

Completed
Last Updated

January 29, 2013

Status Verified

January 1, 2013

Enrollment Period

5 years

First QC Date

September 28, 2005

Last Update Submit

January 26, 2013

Conditions

PTSD

Keywords

Post traumatic stress disorder

Outcome Measures

Primary Outcomes (1)

  • PSS-i

    15 weeks and 1-year follow-up

Study Arms (2)

1

ACTIVE COMPARATOR
Behavioral: Prolonged Exposure (PE) therapy

2

ACTIVE COMPARATOR
Behavioral: Prolonged Exposure (PE) therapy

Interventions

Prolonged Exposure (PE) therapyBEHAVIORAL

20 minutes exposure

1

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • PTSD

You may not qualify if:

  • Psychotic symptoms
  • Dissociation
  • Drug or Alcohol dependence

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Chaim Sheba Medical Center

Ramat Gan, 52621, Israel

Location

MeSH Terms

Conditions

Stress Disorders, Post-Traumatic

Interventions

Therapeutics

Condition Hierarchy (Ancestors)

Stress Disorders, TraumaticTrauma and Stressor Related DisordersMental Disorders

Study Officials

  • Nitza Nacasch, MD

    Sheba Medical Center

    STUDY CHAIR

  • Joseph Zohar, MD

    Sheba Medical Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

September 28, 2005

First Posted

September 29, 2005

Study Start

December 1, 2005

Primary Completion

December 1, 2010

Study Completion

December 1, 2010

Last Updated

January 29, 2013

Record last verified: 2013-01

Locations

IL(1)