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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00184405
Other study ID # 4.2005.393
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date March 2005
Est. completion date December 2008

Study information

Verified date May 2023
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a study evaluating changes in quality of life and global functioning across and after a manualized peer-group preventive intervention for children of parents with psychiatric or addictive problems.


Description:

Self-reported quality of life and based on the group-interviews "ILK" and "Kindl" and general adaptive functioning (CGAS) as reported by teachers and parents will be measured before, after and at follow-up relative to the manualized peer-group preventive intervention. Parents will also complete self-reports on anxiety and depressive symptoms, personality, bonding and attribution before the intervention.


Recruitment information / eligibility

Status Terminated
Enrollment 6
Est. completion date December 2008
Est. primary completion date December 2008
Accepts healthy volunteers No
Gender All
Age group 8 Years to 110 Years
Eligibility Inclusion Criteria: - Family including Parent with psychiatric or addictive problems Exclusion Criteria: - acute severe disorder

Study Design


Locations

Country Name City State
Norway Norwegian University of Science and Technology (NTNU), Faculty of Medicine, Dept. of Neuroscience, Center for Child and Adolescent Mental Health Trondheim

Sponsors (2)

Lead Sponsor Collaborator
Norwegian University of Science and Technology Helse Nord-Trøndelag HF

Country where clinical trial is conducted

Norway,