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Sponsored by: |
Sheba Medical Center |
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Information provided by: | Sheba Medical Center |
ClinicalTrials.gov Identifier: | NCT00229307 |
Comparing the efficacy of 40 minutes PE treatment to 20 minutes of the same treatment
Condition | Intervention |
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PTSD |
Behavioral: Prolonged Exposure (PE) therapy |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Single Blind (Outcomes Assessor), Active Control, Parallel Assignment, Efficacy Study |
Estimated Enrollment: | 20 |
Study Start Date: | December 2005 |
Estimated Study Completion Date: | December 2009 |
Estimated Primary Completion Date: | December 2008 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
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1: Active Comparator |
Behavioral: Prolonged Exposure (PE) therapy
20 minutes exposure
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2: Active Comparator |
Behavioral: Prolonged Exposure (PE) therapy
40 minutes exposure
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Ages Eligible for Study: | 18 Years to 65 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contact: Leah Fostick, MA | +972-3-5357805 | Leah.Fostick@sheba.health.gov.il |
Israel | |
Chaim Sheba Medical Center | Recruiting |
Ramat-Gan, Israel, 52621 | |
Contact: Leah Fostick, MA +972-3-5357805 Leah.Fostick@sheba.health.gov.il |
Study Chair: | Nitza Nacasch, MD | Tel Aviv University |
Principal Investigator: | Joseph Zohar, MD | Tel Aviv University |
Responsible Party: | Chaim Sheba Medical Center ( Prof. Joseph Zohar ) |
Study ID Numbers: | SHEBA-05-3709-JZ-CTIL |
Study First Received: | September 28, 2005 |
Last Updated: | February 14, 2008 |
ClinicalTrials.gov Identifier: | NCT00229307 History of Changes |
Health Authority: | Israel: Israeli Health Ministry Pharmaceutical Administration |
Post traumatic stress disorder |
Anxiety Disorders Mental Disorders Stress Disorders, Post-Traumatic Stress Stress Disorders, Traumatic |
Anxiety Disorders Mental Disorders Stress Disorders, Post-Traumatic Stress Disorders, Traumatic |