Impact of an Integrated Obesity Management System on Patient's Care (ROGMF-2)

This study is ongoing, but not recruiting participants.

Sponsor:

Collaborator:

Canadian Institutes of Health Research (CIHR)

Information provided by (Responsible Party):

Marie-France Langlois, Universitaire de Sherbrooke

ClinicalTrials.gov Identifier:

NCT00991640

First received: October 7, 2009

Last updated: January 14, 2013

Last verified: January 2013

History of Changes

Tracking Information
First Received Date ^ICMJE	October 7, 2009
Last Updated Date	January 14, 2013
Start Date ^ICMJE	November 2009
Estimated Primary Completion Date	December 2013 (final data collection date for primary outcome measure)
Current Primary Outcome Measures ^ICMJE (submitted: October 7, 2009)	Among patients from the targeted diseases group, we aim at improving: a)the proportion of subjects who have an initial intervention planned, according to the CCPGO; b)the proportion of subjects who lose at least 5% of their initial weight. [ Time Frame: 18 months ] [ Designated as safety issue: No ] Among patients from the regular follow-up group, we aim at improving: a)the proportion of patients who have measured weight, BMI and waist circumference and b)the proportion of overweight or obese subjects who have an initial intervention planned. [ Time Frame: 18 months ] [ Designated as safety issue: No ]
Original Primary Outcome Measures ^ICMJE	Same as current
Change History	Complete list of historical versions of study NCT00991640 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures ^ICMJE (submitted: October 7, 2009)	Among health professionals who receive the intervention (vs. those who did not), we aim at ameliorating their attitudes and perceptions towards patients and treatment effectiveness. [ Time Frame: 12 months ] [ Designated as safety issue: No ] Among health professionals who receive the intervention (vs. those who did not), we aim at improving their perception of self-efficacy in managing obesity. [ Time Frame: 12 months ] [ Designated as safety issue: No ] Among health professionals who receive the intervention (vs. those who did not), we aim at increasing their knowledge and expertise on obesity management and changing their practice. [ Time Frame: 12 months ] [ Designated as safety issue: No ] Among patients who are followed by PCPs who receive the intervention (vs. no intervention), we aim at:a) evaluating their attitudes and perceptions regarding obesity/overweight and lifestyle and b)improving their satisfaction regarding their management. [ Time Frame: 18 months ] [ Designated as safety issue: No ]
Original Secondary Outcome Measures ^ICMJE	Same as current
Current Other Outcome Measures ^ICMJE	Not Provided
Original Other Outcome Measures ^ICMJE	Not Provided

Descriptive Information
Brief Title ^ICMJE	Impact of an Integrated Obesity Management System on Patient's Care
Official Title ^ICMJE	Impact of an Integrated Obesity Management System on Patient's Care
Brief Summary	The investigators developed a program aimed at enhancing primary care physician (PCP) teams' expertise, self-efficacy and attitudes with respect to obesity management. The investigators implemented and evaluated this obesity management system based on a preceptorship combined with a virtual learning community favouring continuous support of family medicine groups (FMGs, Groupes de Médecine Familiale) by a team of experts in obesity management; significant improvements regarding their attitudes and perception of self-efficacy were observed immediately after the preceptorship and maintained after one year. Furthermore, the investigators observed significant changes in their practice that were maintained one year later. The investigators hypothesize that their program combining preceptorships with a virtual community will improve: (1) management and weight loss of obese/overweight subjects who are treated by PCPs for hypertension (HTN), type 2 diabetes (DM2) or impaired glucose tolerance (IGT); and (2) screening and initial management of obesity among unselected patients of PCPs who practice in FMGs.
Detailed Description	Not Provided
Study Type ^ICMJE	Interventional
Study Phase	Not Provided
Study Design ^ICMJE	Allocation: Non-Randomized Intervention Model: Parallel Assignment Masking: Single Blind (Subject) Primary Purpose: Health Services Research
Condition ^ICMJE	Obesity
Intervention ^ICMJE	Behavioral: 2-day preceptorship on obesity management
Study Arm (s)	No Intervention: Control No intervention Experimental: Preceptorships Preceptorships with e-learning Intervention: Behavioral: 2-day preceptorship on obesity management
Publications *	Not Provided
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.

Recruitment Information
Recruitment Status ^ICMJE	Active, not recruiting
Estimated Enrollment ^ICMJE	460
Estimated Completion Date	June 2014
Estimated Primary Completion Date	December 2013 (final data collection date for primary outcome measure)
Eligibility Criteria ^ICMJE	Inclusion Criteria: Patients who have, during the past 2 years, at least 4 documented visits for the targeted diseases group and at least 2 visits for the regular follow-up group Exclusion Criteria: Active mental health problem Active psychiatric disorder Cancer in the last five years Patient with medication that changed in the last 6 months
Gender	Both
Ages	18 Years and older
Accepts Healthy Volunteers	Yes
Contacts ^ICMJE	Contact information is only displayed when the study is recruiting subjects
Location Countries ^ICMJE	Canada

Administrative Information
NCT Number ^ICMJE	NCT00991640
Other Study ID Numbers ^ICMJE	09-022
Has Data Monitoring Committee	No
Responsible Party	Marie-France Langlois, Universitaire de Sherbrooke
Study Sponsor ^ICMJE	Universitaire de Sherbrooke
Collaborators ^ICMJE	Canadian Institutes of Health Research (CIHR)
Investigators ^ICMJE	Not Provided
Information Provided By	Universitaire de Sherbrooke
Verification Date	January 2013
^ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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