- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00600418
Identifying Toddlers and Their Parents Who Are Suffering From Posttraumatic Distress Following War and Terror
Identifying Posttraumatic Distress Among Toddlers and Their Parents Following Ongoing Exposure to Terrorism or War
Study Overview
Status
Conditions
Detailed Description
A. Screening of young children and implementation of treatment The screening will consist of self-report questionnaires and a clinical interview with parents, conducted by trained professional about exposure to traumatic events and resulting post-traumatic specific symptoms among the toddlers and their parents. The screening procedure is bases on the accumulated clinical experience and empirical data gained in the ongoing similar project in Sderot. The level of cooperation by parents and teachers in the ongoing project has been exceptionally high, indicating a tremendous need for knowledge, skills and support. Based upon our previous experience, it is anticipated well-baby clinic nurses will also be extremely interested participation.
B. Workshops for parents, teachers, nurses The knowledge and skills of preschool teachers and nurses working in all our projects sights (well baby clinics, day care centers and kindergartens) as well as parents will be increased by providing training regarding the impact of war related trauma on preschool children. Workshops will better equip teachers, nurses and parents with knowledge about the emotional impact of trauma on young children and will increase the skills to help preschool children contain emotional distress as well as to help them in coping with the emotional consequences of trauma exposure.
C. Treatment Interventions All toddlers identified with posttraumatic distress will receive dyadic treatment focused on dealing with posttrauma. Dyadic treatment involving parents and children is aimed at increasing the attunement of parents to their toddlers and their needs in times of crises. Local practitioners in Sderot implementing this cutting-edge treatment received specialized training adjusted to the context of terror and trauma by a child trauma specialist from Mount Sinai Medical Center in New York.
D. Evaluation of treatment Evaluation of treatment efficacy (dyadic treatment) will be assessed by pre and post interviews that will be conducted by trained professionals with all parents participating in the dyadic treatments in each of the three cities
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Jerusalem, Israel
- Isreal Center for the Treatment of Psychotrauma
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Families with children between the age 1-6 years.
- Families living in Sderot, Kyriat Shmona and Haifa
Exclusion Criteria:
- Severe developmental problems
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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PTSD and behavioral and emotional problems
Time Frame: April 2007- December 2008
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April 2007- December 2008
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
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Maternal depression and PTSD
Time Frame: Aprol 2007- December 2008
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Aprol 2007- December 2008
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Other Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Maternal flexibility
Time Frame: April 2008- December 2008
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April 2008- December 2008
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Ruth Pat-Horenczyk, Ph.d, Isreal Center for the Treatment of Psychotrauma
- Principal Investigator: Ruth Pat-Horenczyk, Ph.D, The Israel Center for the Treatment of Psychotrauma
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Rpat2CTIL
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