Effect of Post Traumatic Stress Disorder on Parenting

The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2012 by Hadassah Medical Organization.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
Hillel Yaffe Medical Center
Information provided by (Responsible Party):
Rena Cooper, Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT01656655
First received: August 1, 2012
Last updated: August 2, 2012
Last verified: August 2012
  Purpose

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.


Condition
Post Traumatic Stress Disorder

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Cross-Sectional
Official Title: Parenting With and Without PTSD: The Effect of Attachment, Symptoms and Posttraumatic Growth

Resource links provided by NLM:


Further study details as provided by Hadassah Medical Organization:

Estimated Enrollment: 120
Study Start Date: May 2012
Estimated Study Completion Date: June 2013
Estimated Primary Completion Date: December 2012 (Final data collection date for primary outcome measure)
Groups/Cohorts
PTSD group
Patients with PTSD
Control Group
non PTSD group

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Sampling Method:   Non-Probability Sample
Study Population

patients with ptsd

Criteria

Inclusion Criteria:

  • ptsd (PSS>15) children under age 18

Exclusion Criteria:

  • non ptsd (pss<15) children under age 18
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01656655

Contacts
Contact: Rena Cooper, MD 972544704636 crena@hadassah.org.il

Locations
Israel
Hadassah Medical Organization Recruiting
Jerusalem, Choose a State, Israel, 92200
Contact: Sara Freedman, PhD    972544704636    sarafreedman@gmail.com   
Contact: Rena Cooper, MD       crena@hadassah.org.il   
Sub-Investigator: Sara Freedman, PhD         
Principal Investigator: Rena Cooper, MD         
Sponsors and Collaborators
Hadassah Medical Organization
Hillel Yaffe Medical Center
Investigators
Principal Investigator: rena Cooper, MD Hadassah Medical Organization
  More Information

No publications provided

Responsible Party: Rena Cooper, Head Outpatient Psychiatry, Hadassah Medical Organization
ClinicalTrials.gov Identifier: NCT01656655     History of Changes
Other Study ID Numbers: PTSDpar-2-hmo
Study First Received: August 1, 2012
Last Updated: August 2, 2012
Health Authority: Israel: Ministry of Health

Keywords provided by Hadassah Medical Organization:
ptsd, parenting

Additional relevant MeSH terms:
Disease
Stress Disorders, Post-Traumatic
Stress Disorders, Traumatic
Anxiety Disorders
Mental Disorders
Pathologic Processes

ClinicalTrials.gov processed this record on October 23, 2014