Changes Following Inpatient Child-oriented Family Treatment
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|ClinicalTrials.gov Identifier: NCT00184327|
Recruitment Status : Completed
First Posted : September 16, 2005
Last Update Posted : January 18, 2017
Children receiving IFT (intensive family therapy) were assessed for symptom profile and global functioning before admission, 3 months after discharge and 1 year after discharge. Children were assessed by parents, children, their teachers and themselves. Parents were assessed by themselves at the same points in time through psychological self-report questionnaires.
The study is intended to explore covariates to change in children as well as in parents during (pre-treatment) the treatment and follow-up periods.
|Condition or disease||Intervention/treatment|
|Psychiatric Disorders||Behavioral: Intensive family therapy - inpatient Behavioral: Diagnostic assessment - child and adolescent psychiatry|
IFT is an intensive combinatory family treatment which is child-oriented, and traditionally used in an inpatient family treatment unit in child and adolescent psychiatry.
Measures include ones on bonding (PBI), personality traits (NEO-PI), anxiety and depressive symptoms (HADS), attributional tendencies (PAT) and social desirable responding (BIDR). A subgroup was also assessed before a waiting period (pre-treatment).
|Study Type :||Observational|
|Actual Enrollment :||150 participants|
|Official Title:||Change Across Intensive Inpatient Family Treatment in Child and Adolescent Psychiatry. A Multi-site Study of Parents and Children in Inpatient Family Treatment|
|Study Start Date :||January 2002|
|Actual Primary Completion Date :||December 2006|
|Actual Study Completion Date :||June 2008|
- Behavioral: Intensive family therapy - inpatient
2-4 weeks (5days) family inpatient assessment and treatment
- Behavioral: Diagnostic assessment - child and adolescent psychiatry
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): NCT00184327
|Haukeland University Hospital, Helse Bergen|
|Norwegian University of Science and Technology (NTNU), Faculty of Medicine, Dept. of Neuroscience, Center for Child and Adolescent Mental Health|
|Trondheim, Norway, N-7089|
|Principal Investigator:||Tormod Rimehaug, Asst. Prof.||Norwegian University of Science and Technology (NTNU), Faculty of Medicine, Dept. of Neuroscience, Center for Child and Adolescent Mental Health|