Chrysalis Day Program Body Mass Index Study
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00202215|
Recruitment Status : Completed
First Posted : September 20, 2005
Last Update Posted : October 16, 2007
|Condition or disease||Intervention/treatment||Phase|
|Borderline Personality Disorder Eating Disorders||Behavioral: Chrysalis Day Program||Not Applicable|
As part of the Providence Continuing Care Center's continuing quality improvement initiatives this study is to more systematically evaluate the success of the Chrysalis Day Hospital Program in dealing with some features of eating disorders commonly experienced by its patients.
At intake all clients will be approached to give informed consent to participate. If they do consent they will have their height and weight recorded( if they request they will not be told their weight)as part of the usual intake process conducted by a dietician.
When clients exit the program they again will be approached to be weighed. The body mass index will be calculated and compared to admission values.
The Chrysalis Program is a unique day hospital approach to treating individuals with severe personality disorders (primarily Borderline)that views the eating disordered behaviour common to these clients as a symptom of many and by addressing core issues of affect dysregulation as well as psychoeducation about eating the eating problems will improve .
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||106 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Study on the Effects of a Personality Disorder Day Hospital Program on Clients Body Mass Index|
|Study Start Date :||October 2001|
|Actual Study Completion Date :||June 2007|
- Body Mass Index at time of enrolling in programme and at leaving [ Time Frame: at entry and upon leaving the program ]
- patient demographics relationship to outcome [ Time Frame: upon entry and exit from the program ]
- programme changes and relation to outcome [ Time Frame: from start to the end of the study ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00202215
|Providence Care Centre Mental Health Services|
|Kingston, Ontario, Canada, K7L 4X3|
|Principal Investigator:||Stephen H McNevin, MD||Queens University|