- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06529666
Medical Residents Learning Weight Management Counseling Skills (MRWeight)
MRWeight: Medical Residents Learning Weight Management Counseling Skills -- A Multi-Modal, Technology-Assisted, Spaced Education Program
The goal of this study is to addresses the lack of weight management training physicians receive during their residency training. The main questions it aims to answer are:
- How affective is the MRWeight curriculum at increasing medical residents weight management counseling (WMC) skills.
- Evaluate residents' adoption of WMC skills in encounters with their patients
- what would be the best way to get residents to adopt the WMC skills Residents in the comparison group will receive a course on obesity and weight management. The residents in the intervention group will have to attend 2 informational sessions and will receive 6 email modules on WMC. Both groups will also take part in 3 assessments over the course of 18 months to see which group has better WMC skills.
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: RAJANI SADASIVAM, PhD
- Phone Number: 68923 (508) 856-8989
- Email: Rajani.Sadasivam@umassmed.edu
Study Locations
-
-
California
-
Palo Alto, California, United States, 94304
- Recruiting
- Stanford University
-
Contact:
- Kim Chiang, MD
- Phone Number: 650-498-9000
- Email: kichiang@stanford.edu
-
Principal Investigator:
- Kim Chiang, MD
-
Sacramento, California, United States, 95820
- Recruiting
- UC Davis
-
Contact:
- Stephany Sanchez, MD
- Phone Number: 800-282-3284
- Email: stesanchez@UCDAVIS.EDU
-
Principal Investigator:
- Stephany Sanchez, MD
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02118
- Not yet recruiting
- Boston University
-
Contact:
- Juhee McDougal, MD
- Phone Number: 617-414-5951
- Email: jcmcd@bu.edu
-
Principal Investigator:
- Juhee McDougal, MD
-
-
New York
-
East Setauket, New York, United States, 11733
- Recruiting
- Stony Brook
-
Contact:
- Patricia NG, MD
- Phone Number: 631-444-4630
- Email: Patricia.Ng@stonybrookmedicine.edu
-
Principal Investigator:
- Patricia NG, MD
-
The Bronx, New York, United States, 10467
- Recruiting
- Albert Einstein College of Medicine
-
Contact:
- Jing Yu Pan, MD
- Phone Number: 718-920-2273
- Email: jpan1@montefiore.org
-
Principal Investigator:
- Jing Yu Pan, MD
-
-
Pennsylvania
-
Hershey, Pennsylvania, United States, 17033
- Recruiting
- Penn State University
-
Contact:
- Eliana Hempel, MD
- Phone Number: 717-531-5160
- Email: ehempel@pennstatehealth.psu.edu
-
Principal Investigator:
- Eliana Hempel, MD
-
Philadelphia, Pennsylvania, United States, 19140
- Recruiting
- Temple University
-
Contact:
- Sharon Herring, MD, MPH
- Phone Number: 800-836-7536
- Email: sharon.herring@temple.edu
-
Principal Investigator:
- Sharon Herring, MD,MPH
-
-
Texas
-
Houston, Texas, United States, 77030
- Recruiting
- Houston Methodist
-
Contact:
- Melina Awar, MD
- Phone Number: 713-441-0006
- Email: mawar@houstonmethodist.org
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Principal Investigator:
- Melina Awar, MD
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All PGY1 residents in participating sites
Inclusion Criteria for participating site:
- The program is willing and able to incorporate the MRWeight program into the PGY1 core curriculum.
- The residency director will allow PGY1s to complete surveys and curriculum evaluations online or in class and to complete a standardized assessment of their knowledge and use of WMC, and
- The site will allow inclusion of three successive cohorts of PGY1s to ensure more than a sufficient number of residents to adequately test the effect of the intervention
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Comparison Arm
Residents in comparison arm receive a core foundation course and will take part in all 3 assessments (including 3 surveys and 2 video communication assessments) over the course of 18 months.
|
Residents will receive a core foundation slides on weight management counselling
|
|
Experimental: Intervention Arm
Residents in the intervention arm will receive (in addition to the core foundation course) 6 email modules and practice video communication assessments on weight management counseling.
They will also attend 2 educational session and take part in all 3 assessments (including 3 surveys and 2 video communication assessments) over the course of 18 months.
|
Residents will receive a core foundation slides on weight management counselling
A 45-minute foundational presentation covering key Weight Management Counseling (WMC) concepts, obesity bias, and cultural humility facilitated by a trained clinician-educator at the residency program delivered at baseline.
6 email modules delivered over months 2-8). Each 3P module will allow the resident to: (1) Prepare: Review relevant concepts and demonstration videos sent via an email to prepare for completing the VCA vignettes; (2) Practice: Respond to brief vignettes of various 5As WMC challenging scenarios by audio recording their spoken response on the VCA tool; and (3) Process: Reflect on actionable expert and crowdsourced analogue patient feedback on the quality of their responses to each VCA vignette.
(months 8-10): This 45-minute session will discuss key barriers to WMC adoption in clinical practice using real-world cases captured from residents facilitated by a trained clinician-educator at the residency program.
2 emails in months 10-12 covering key concepts in the preceding components.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
WMC skills VCA (video Communications assessment) assessment
Time Frame: Completed during month 1 and again at month 12 post recruitment.
|
Residents in both arms will be asked to complete the assessment VCA vignettes that will include a series of vignettes representing challenging cases.
4-6 trained raters blinded to the residents' study arm (intervention vs. comparison) will rate the residents' responses.
|
Completed during month 1 and again at month 12 post recruitment.
|
|
Change in WMC skills assessment
Time Frame: Completed during months 1, 12 and 18 post recruitment.
|
This measure will be assessed using an online survey at baseline (study start), at 12 months, and 18 months.
|
Completed during months 1, 12 and 18 post recruitment.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in adoption scale Scores at eighteen months
Time Frame: Completed during months 1, 12 and 18 post recruitment.
|
This measure will be assessed using Adoption scale (7-item checklist assessing resident adoption of WMC skills in their encounters with patients in clinical practice) on a 5-point on a Likert Scale [never (0) to always (4)].
|
Completed during months 1, 12 and 18 post recruitment.
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Rajani Sadasivam, PhD, UMass Chan Medical School
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00000691
- 1R01DK134372-01 (U.S. NIH Grant/Contract)
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
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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