Evaluation of a Six-session Psycho-education Group Program

Sponsor
Norwegian University of Science and Technology (Other)
Overall Status
Terminated
CT.gov ID
NCT00400933
Collaborator
The Royal Norwegian Ministry of Health (Other)
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Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: psycho-education
Phase 1

Detailed 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Evaluation of a Six-session Psycho-education Group Program Delivered to Family Members and Close Friends of Patients Suffering From Eating Disorders and Co-morbid Personality Disorders
Study Start Date :
Nov 1, 2006
Actual Primary Completion Date :
Dec 1, 2008
Actual Study Completion Date :
Dec 1, 2009

Arms and Interventions

Arm Intervention/Treatment
Experimental: psycho-education

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

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

Outcome Measures

Primary Outcome Measures

  1. Scores on perceived caregiver burden (Experience of Caregiving Inventory [ECI]) [1 year]

Secondary Outcome Measures

  1. Scores on general health and relational variables [1 year]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 67 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Østmarka Psychiatric Department, St Olavs Hospital, University Hospital of Trondheim Trondheim Norway 7044

Sponsors and Collaborators

  • Norwegian University of Science and Technology
  • The Royal Norwegian Ministry of Health

Investigators

  • Principal Investigator: Are Holen, PhD MD, Norwegian University of Science and Technology

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:
NCT00400933
Other Study ID Numbers:
  • 4,2006.2005
First Posted:
Nov 17, 2006
Last Update Posted:
Feb 13, 2012
Last Verified:
Feb 1, 2012
Keywords provided by Norwegian University of Science and Technology
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 13, 2012