- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04658550
Remote vs In Person Weight Loss Study
A Mixed Retrospective-prospective, Observational Study Evaluating the Efficacy of Counselling in a Remote Setting Compared to an In-person Setting on Weight Loss, in Obese Patients With Body Mass Index > 35 Kg/m2 and Enrolled in the Behaviour Modification Program at the Bariatric Centre of Excellence at St Joseph's Healthcare Hamilton.
The COVID-19 pandemic has created fear, financial difficulties and interruptions in the lives of patients and healthcare providers. As a result, many patients suffering from chronic conditions such as obesity have had their treatment disrupted by the pandemic. The Bariatric Medical Weight Management Clinic at St. Joseph's Healthcare Hamilton transitioned its weight loss and maintenance counselling classes to a remote (online) platform in response to the pandemic. The remote weight loss and maintenance classes allows patients to continue receiving treatment for obesity from their homes. The remote weight loss and maintenance program is conducted on a safe platform that has been thoroughly reviewed and approved by St. Joseph's Privacy Committees.
The aim of this study is to learn whether the remote weight loss and maintenance classes can lead to similar weight loss compared to the in-person weight loss and maintenance classes that were offered to patients before the COVID-19 pandemic. This study also aims to gather feedback about the program to improve its delivery and patients' experiences.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The COVID-19 pandemic has created fear, financial difficulties and interruptions in the lives of patients and healthcare providers. As a result, many patients suffering from chronic conditions such as obesity have had their treatment disrupted by the pandemic. The Bariatric Medical Weight Management Clinic at St. Joseph's Healthcare Hamilton transitioned its behaviour modification program, also known as weight loss and maintenance counselling classes, to a remote (online) platform in response to the pandemic. The remote weight loss and maintenance classes allow patients to continue receiving treatment for obesity from their homes.
This is a 26-week, single-centre, mixed retrospective and prospective, observational study evaluating the efficacy of counselling in a remote setting compared to an in-person setting in achieving weight loss among adult patients with obesity enrolled in the behaviour modification program. This study also aims to gather feedback about the program to improve its delivery and patients' experiences.
Approximately 120 patients participating in the behaviour modification program and providing informed consent will be observed in this study. This study involves a prospective and retrospective component. The prospective component will be an observational study of 60 subjects who will receive 26-weeks of weight loss and maintenance counselling in a remote setting and a low-calorie meal replacement as part of their usual care. The retrospective component will involve using historical data from 60 subjects who received 26-weeks of weight loss and maintenance counselling in an in-person setting and a low-calorie meal replacement as part of their usual care.
Parameters measured as part of standard of care at the start and end of the program, such as body weight, blood pressure and lab tests will be collected for analysis of study endpoints. Participants will also be asked to complete a satisfaction survey at the end. There will be no blinding of patients, study investigators, or data analysts.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Ontario
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Hamilton, Ontario, Canada, L9C0E3
- St Joseph's Healthcare Hamilton
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- ≥ 18 years of age
- Enrolled in 26-week BCoE behaviour modification program with meal replacements
- Able and willing to provide signed informed consent
Exclusion Criteria:
- Subjects will be excluded if they contact clinic or study personnel to withdraw consent or withdraw data from the study.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Remote Weight Loss Behaviour Modification Program with Meal Replacements
This is the prospective study group who will receive 26-weeks of weight loss and maintenance counselling in a remote setting and a low-calorie meal replacement as part of their usual care.
|
The standard of care behaviour modification program for weight loss will be offered virtually due to the COVID-19 pandemic (prospective).
|
|
In Person Weight Bahaviour Modification Program with Meal Replacements
This is the retrospective study group who received 26-weeks of weight loss and maintenance counselling in person and a low-calorie meal replacement as part of their usual care.
|
The standard of care behaviour modification program for weight loss was offered in person prior to the COVID-19 pandemic (retrospective).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mean Percentage Change in Body Weight
Time Frame: Baseline to Week 26
|
To evaluate the efficacy of counselling in a remote setting compared to an in-person setting in achieving weight loss among adult patients with obesity enrolled in the behaviour modification program
|
Baseline to Week 26
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient satisfaction and barriers to participation
Time Frame: Week 26
|
Patient satisfaction and barriers to participation associated with the remote weight loss and maintenance program as assessed by the Bariatric Centre of Excellence Virtual Medical Program Satisfaction Survey.
|
Week 26
|
|
Change in blood pressure
Time Frame: Baseline to Week 26
|
Change in blood pressure
|
Baseline to Week 26
|
|
Change in lipid profile
Time Frame: Baseline to Week 26
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Change in lipid profile including total cholesterol, triglycerides, low density lipoprotein and high density lipoprotein
|
Baseline to Week 26
|
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Change in fasting blood glucose
Time Frame: Baseline to Week 26
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Change in fasting blood glucose
|
Baseline to Week 26
|
|
Change in heart rate
Time Frame: Baseline to Week 26
|
Change in heart rate
|
Baseline to Week 26
|
|
Change in HbA1C
Time Frame: Baseline to Week 26
|
Change in HbA1C
|
Baseline to Week 26
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Tony Chetty, MD, St. Joseph's Healthcare Hamilton
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Remote v In Person Weight Loss
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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