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| Tracking Information | |||||||||
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| First Received Date † | November 16, 2006 | ||||||||
| Last Updated Date | July 17, 2007 | ||||||||
| Start Date † | November 2006 | ||||||||
| Current Primary Outcome Measures † |
Scores on perceived caregiver burden (Experience of Caregiving Inventory [ECI]) | ||||||||
| Original Primary Outcome Measures † | Same as current | ||||||||
| Change History | Complete list of historical versions of study NCT00400933 on ClinicalTrials.gov Archive Site | ||||||||
| Current Secondary Outcome Measures † |
Scores on general health and relational variables | ||||||||
| Original Secondary Outcome Measures † | Same as current | ||||||||
| Descriptive Information | |||||||||
| Brief Title † | Evaluation of a Six-Session Psychoeducation Group Program | ||||||||
| Official Title † | Evaluation of a Six-Session Psychoeducation Group Program Delivered to Family Members and Close Friends of Patients Suffering From Eating Disorders and Comorbid Personality Disorders | ||||||||
| Brief Summary | The purpose of this project is to analyse the impact of a psychoeducational group programme on the family members and close friends of persons with eating disorders and comorbid personality disorders. |
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| Detailed Description | The aim of this project is to analyse the impact of a six session psychoeducational group programme on the family members and close friends of persons with eating disorders and comorbid 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. |
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| Study Phase | Phase I | ||||||||
| Study Type † | Interventional | ||||||||
| Study Design † | Health Services Research, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study | ||||||||
| Condition † |
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| Intervention † | Procedure: psychoeducation | ||||||||
| Study Arms / Comparison Groups | |||||||||
| Publications * | |||||||||
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* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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| Recruitment Information | |||||||||
| Recruitment Status † | Recruiting | ||||||||
| Enrollment † | 50 | ||||||||
| Estimated Completion Date | November 2010 | ||||||||
| Primary Completion Date | |||||||||
| Eligibility Criteria † | Inclusion Criteria:
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| Gender | Both | ||||||||
| Ages | 18 Years to 67 Years | ||||||||
| Accepts Healthy Volunteers | Yes | ||||||||
| Contacts †† |
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| Location Countries † | Norway | ||||||||
| Expanded Access Status | |||||||||
| Administrative Information | |||||||||
| NCT ID † | NCT00400933 | ||||||||
| Responsible Party | |||||||||
| Secondary IDs †† | |||||||||
| Study Sponsor † | Norwegian University of Science and Technology | ||||||||
| Collaborators †† | The Royal Norwegian Ministry of Health | ||||||||
| Investigators † |
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| Information Provided By | Norwegian University of Science and Technology | ||||||||
| Verification Date | November 2006 | ||||||||
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† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |
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