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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 * | |||||||||
* 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 | ||||||||
† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |