- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02226393
Evaluating Effectiveness of Dyadic Prolonged Exposure on 2-4 Years Old vs. Toddler-parent Focused Treatment
Evaluating Effectiveness of Dyadic Prolonged Exposure Treatment on 2-4 Years Old vs. Toddler-parent Focused Treatment
Traumatic events have potentially debilitating long-lasting effects on the child's normal development and, therefore, should be effectively treated. Prolonged Exposure (PE) therapy has been found to be effective in reducing posttraumatic stress disorder symptoms in adults and in adolescents. It has not yet been tested in toddlers.
The purpose of this study is to examine the treatment efficacy of 2 methods of treatment for toddlers with PTSD and their parents. A randomized control trial could examine the efficacy of PE versus dyadic play therapy (TP-CT). Exploration of these questions under more rigorous conditions would help broaden our knowledge about developmentally sensitive treatment tools for this age group.
Our research hypotheses are:
- PE would more effective than TP-CT in reducing post-traumatic symptoms in toddlers.
- PE would more effective than TP-CT in reducing post-traumatic symptoms of the toddlers' parents.
- These results will be preserved in a follow-up of 3-6 months post treatment. Following psychiatric assessment, 100 toddlers will be randomly assigned to PE and TP-CT (50 participants in each group).
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Petah-Tikva, Israel
- Rabin Medical Center
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Tel Aviv, Israel
- Association for Children at Risk's Cohen Harris Resilience Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Hebrew speaking toddlers with PTSD related to traumatic experience that occured at least 1 month prior to the study enrollment
- Toddlers whose parents are living together
Exclusion Criteria:
- Toddlers which are still dealing with an active life threatening illness and are hence going through medical procedures.
- Toddlers with intelectual developmental disorder
- Toddlers with an active psychosis
- Toddlers with blindness or deafness
- Toddlers who are currently taking psychotropic medication
- Toddlers and parents that receive psycotherapy outside of the study for their PTSD symptoms
- Toddlers diagnozed with autism spectrum disorder
- Toddlers who were exposed to domestic or sexual violence
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Prolonged exposure
See intervention description
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The PE treatment includes 12-15 60 minutes' sessions.
The 2 main components of the treatment are psychoeducation about common reactions to trauma and in-vivo exposures (gradual exposure to trauma related situations and objects) and repeated recounting of the traumatic memory, Trauma memory recounting and in-vivo exposures are conducted during several successive sessions so the child learns that the exposures themselves pose no real harm to him, indicating that when one confronts what one is afraid of it becomes easier to manage.
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Active Comparator: Child-parent Play Therapy
see intervention description
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Is consisted of 12-15 weekly 60 minute sessions of parent-child centered therapy it focus on establishing a trusting, empowering, and validating therapeutic relationship.
Participants are allowed to choose when, how, and whether or not to address their trauma memory.
Therapists provide active listening, empathy,and encouragement to talk about feelings and express belief in the participants ability to cope.
In sessions 4 and 8, participants are asked how they feel about their trauma.
With this exception, participants direct the sessions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Change from baseline in post traumatic symptoms: clinical assessment and Young child ptsd checklist (YCPC, Scheeringa & Haslett, 2010).
Time Frame: Parents' pre-treatment, post treatment and follow-up 3,6,12 months post treatment
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Change from baseline in post traumatic symptoms will be assessed using the Classification of Mental Health and Developmental Disorders of Infancy and Early Childhood) and the Young Child PTSD Checklist (YCPC, Scheeringa & Haslett, 2010).
The YCPC assesses probable diagnosis formed the basis for the new DSM-5 disorder for posttraumatic stress disorder for children 6 years and younger.
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Parents' pre-treatment, post treatment and follow-up 3,6,12 months post treatment
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Beck Depression Inventory (BDI)
Time Frame: Parents' pre-treatment, post treatment (after 12-15 sessions) and follow-up 3-6 months post treatment
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A self-report questionnaire for depression among adults
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Parents' pre-treatment, post treatment (after 12-15 sessions) and follow-up 3-6 months post treatment
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The Posttraumatic Stress Symptom Scale-Self report (PSS-SR; Foa, Riggs, Dancu & Rothbaum, 1993)
Time Frame: Parents' pre-treatment, during treatment (every 2 sessions), post treatment (after 12-15 sessions) and follow-up 3-6 months post treatment
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A self report questionnaire for the assessment of PTSD symptoms among adults
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Parents' pre-treatment, during treatment (every 2 sessions), post treatment (after 12-15 sessions) and follow-up 3-6 months post treatment
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Posttraumatic Stress Cognitions Inventory (PTCI)
Time Frame: Parents' pre-treatment, post treatment (after 12-15 sessions) and follow-up 3-6 months post treatment
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A self report questionnaire assessing post traumatic beliefs in adults
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Parents' pre-treatment, post treatment (after 12-15 sessions) and follow-up 3-6 months post treatment
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Parenting Sense of Competence Scale )PSOC; Gibaud -Wallstton & Wandersman, 1978)
Time Frame: Parents' pre-treatment, post treatment (after 12-15 sessions) and follow-up 3-6 months post treatment
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The Parenting Sense of Competency Scale (PSOC) was developed by Gibaud-Wallston as part of her PhD dissertation and presented at the American Psychological Association by Gibaud-Wallston and Wandersman in 1978.
The PSOC is a 17 item scale, with 2 subscales.
Each item is rated on a 6 point Likert scale anchored by 1 = "Strongly Disagree" and 6 = "Strongly Agree".
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Parents' pre-treatment, post treatment (after 12-15 sessions) and follow-up 3-6 months post treatment
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Orit Krispin, Phd, Schneider Children's Medical Center, Israel
- Study Director: Lilach Rachamim, Phd
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RMC147804ctil
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