Trauma-focused Cognitive-behavioural Therapy(TF-CBT) for Children: A Study of Process and Outcome.
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|ClinicalTrials.gov Identifier: NCT00635752|
Recruitment Status : Completed
First Posted : March 14, 2008
Last Update Posted : April 23, 2015
|Condition or disease||Intervention/treatment||Phase|
|Post-Traumatic Stress Disorder||Other: TF-CBT Other: Treatment as Usual (TAU)||Not Applicable|
Children experiencing traumas, such as sexual abuse, physical abuse, domestic violence, serious accidents, or natural disasters, may develop severe health problems.
This study will examine the short and long-term effects of trauma-focused cognitive-behavioural therapy on children exposed to serious trauma, and moderating factors of treatment outcome.
The study will use a random control design, and will be implemented in regular clinical practice in Norway.
More knowledge within this field is important for practitioners as well as policy makers in planning interventions and therapy for children and their caregivers.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||156 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Triple (Participant, Care Provider, Outcomes Assessor)|
|Official Title:||Trauma-focused Cognitive-behavioural Therapy for Children: A Study of Process and Outcome.|
|Study Start Date :||April 2008|
|Actual Primary Completion Date :||February 2011|
|Actual Study Completion Date :||August 2013|
Participants will receive trauma-focused cognitive behavioral therapy (TF-CBT)
TF-CBT sessions will include trauma-focused treatment, and will teach participants behavioral and coping skills.
Active Comparator: 2
Participants will receive sessions of treatment as usual (TAU)
Other: Treatment as Usual (TAU)
Participants will receive regular therapy as is usually practiced in clinics
Other Name: TAU
- PTSD [ Time Frame: Before session, middle, end, one year follow-up, 18 month follow-up ]
- Parent distress [ Time Frame: Before session, middle, end, one year follow-up, 18 month follow-up ]
- Therapeutic alliance [ Time Frame: After 1st. and 6th. session ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00635752
|Norwegian center for violence and traumatic stress studies|
|Principal Investigator:||Tine K Jensen, PhD||Norwegian Centre for Violence and Traumatic Stress Studies|