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Obesity Management Training for Obesity (ROGMF-2 Trial)
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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
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 18 months
Awards & highlights
ROGMF-2 Trial Summary
This trial combined a preceptorship with a virtual learning community in order to help primary care physician teams manage obesity more effectively. The team observed significant improvements in attitudes and self-efficacy among the participants, which were maintained after one year.
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.Check my eligibility
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.See study design
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.
ROGMF-2 Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 18 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~18 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
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.
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.
Secondary outcome measures
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.
Among health professionals who receive the intervention (vs. those who did not), we aim at improving their perception of self-efficacy in managing obesity.
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.
+1 moreROGMF-2 Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: PreceptorshipsExperimental Treatment1 Intervention
Preceptorships with e-learning
Group II: ControlActive Control1 Intervention
No intervention
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Who is running the clinical trial?
Université de SherbrookeLead Sponsor
292 Previous Clinical Trials
68,981 Total Patients Enrolled
13 Trials studying Obesity
2,175 Patients Enrolled for Obesity
Canadian Institutes of Health Research (CIHR)OTHER_GOV
1,341 Previous Clinical Trials
26,452,253 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
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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.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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