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Obesity Management Training for Obesity (ROGMF-2 Trial)
N/A
Waitlist Available
Led By Marie-France Langlois, MD
Research Sponsored by Université de Sherbrooke
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Must not have
History of cancer in the last five years
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
No Placebo-Only Group
Summary
This trial tests a program that helps doctors manage obesity better through expert mentorship and online support. It targets obese or overweight patients with conditions like hypertension and diabetes, aiming to improve doctors' skills and confidence in treating these patients.
Who is the study for?
This trial is for patients who have had at least four documented visits in the past two years for conditions like hypertension, type 2 diabetes, or impaired glucose tolerance. It's designed to help primary care physician teams improve their management of obesity.
What is being tested?
The study tests an integrated obesity management system that includes a short training program (preceptorship) and ongoing support through a virtual community. The goal is to see if this improves weight loss and obesity care among patients with certain chronic diseases.
What are the potential side effects?
Since this trial focuses on education and support systems rather than medication or medical procedures, there are no direct side effects from interventions being studied.
Eligibility Criteria
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have had cancer within the last five years.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: PreceptorshipsExperimental Treatment1 Intervention
Preceptorships with e-learning
Group II: ControlActive Control1 Intervention
No intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
The most common treatments for obesity, particularly those involving educational and supportive interventions like the Preceptorship and Virtual Learning Community trial, focus on lifestyle modifications. These include dietary changes to reduce caloric intake, increased physical activity to boost energy expenditure, and behavioral therapy to modify habits contributing to weight gain.
These mechanisms are essential for obesity patients as they tackle the underlying causes of obesity, support sustainable weight loss, and enhance overall health and well-being.
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Who is running the clinical trial?
Université de SherbrookeLead Sponsor
304 Previous Clinical Trials
76,269 Total Patients Enrolled
14 Trials studying Obesity
2,222 Patients Enrolled for Obesity
Canadian Institutes of Health Research (CIHR)OTHER_GOV
1,388 Previous Clinical Trials
26,517,613 Total Patients Enrolled
56 Trials studying Obesity
9,301 Patients Enrolled for Obesity
Marie-France Langlois, MDPrincipal InvestigatorUniversité de Sherbrooke
7 Previous Clinical Trials
1,550 Total Patients Enrolled
4 Trials studying Obesity
1,108 Patients Enrolled for Obesity
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- My medication has changed in the last 6 months.I've had at least 4 visits for my condition and 2 follow-ups in the last 2 years.I have had cancer within the last five years.
Research Study Groups:
This trial has the following groups:- Group 1: Control
- Group 2: Preceptorships
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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