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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01656655
Other study ID # PTSDpar-2-hmo
Secondary ID
Status Recruiting
Phase N/A
First received August 1, 2012
Last updated August 2, 2012
Start date May 2012
Est. completion date June 2013

Study information

Verified date August 2012
Source Hadassah Medical Organization
Contact Rena Cooper, MD
Phone 972544704636
Email crena@hadassah.org.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

PTSD affects a wide variety of symptoms, some of which have been shown to disrupt family relationships. This study will examine some of the effects on parenting, from the perspective of the parent with PTSD.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date June 2013
Est. primary completion date December 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- ptsd (PSS>15) children under age 18

Exclusion Criteria:

- non ptsd (pss<15) children under age 18

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Locations

Country Name City State
Israel Hadassah Medical Organization Jerusalem Choose a State

Sponsors (2)

Lead Sponsor Collaborator
Hadassah Medical Organization Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

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