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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00400933
Other study ID # 4,2006.2005
Secondary ID
Status Terminated
Phase Phase 1
First received November 16, 2006
Last updated February 9, 2012
Start date November 2006
Est. completion date December 2009

Study information

Verified date February 2012
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority Norway: Norwegian Social Science Data Services
Study type Interventional

Clinical Trial Summary

The aim of this project is to analyze the impact of a psycho-educational group program on the family members and close friends of persons with eating disorders and co-morbid personality disorders.


Description:

The aim of this project is to analyze the impact of a six session psycho-educational group program on the family members and close friends of persons with eating disorders and co-morbid personality disorders.

Measurements: General health, perceived caregiver burden, and relation to the patient at the following point of time: pre -, post- and follow up, with waiting list control.


Recruitment information / eligibility

Status Terminated
Enrollment 10
Est. completion date December 2009
Est. primary completion date December 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 67 Years
Eligibility Inclusion Criteria:

- Relatives and close friends to persons receiving treatment for their eating disorder and comorbid personality disorder.

- > 18 years,

- Speak and understand norwegian language, and

- Informed consent to participate for both relative and patient.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Behavioral:
psycho-education
six session psycho-educational group program for family members and close friends of persons with eating disorders and co-morbid personality disorders

Locations

Country Name City State
Norway Østmarka Psychiatric Department, St Olavs Hospital, University Hospital of Trondheim Trondheim

Sponsors (2)

Lead Sponsor Collaborator
Norwegian University of Science and Technology The Royal Norwegian Ministry of Health

Country where clinical trial is conducted

Norway, 

Outcome

Type Measure Description Time frame Safety issue
Primary Scores on perceived caregiver burden (Experience of Caregiving Inventory [ECI]) 1 year No
Secondary Scores on general health and relational variables 1 year No
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