Extension of the 5As Team Study for Improved Provider Obesity Management to Physicians and Medical Trainees (Part 2) (5AsT-MD2)
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|ClinicalTrials.gov Identifier: NCT02648308|
Recruitment Status : Completed
First Posted : January 7, 2016
Last Update Posted : February 23, 2018
|Condition or disease||Intervention/treatment|
|Obesity||Behavioral: Obesity Management Workshop|
Show Detailed Description
|Study Type :||Observational|
|Actual Enrollment :||75 participants|
|Official Title:||Extension of the 5As Team Study for Improved Provider Obesity Management to Physicians and Medical Trainees (Part 2)|
|Actual Study Start Date :||October 8, 2015|
|Actual Primary Completion Date :||April 6, 2017|
|Actual Study Completion Date :||August 27, 2017|
Behavioral: Obesity Management Workshop
- Changes in Attitudes Towards Obese Persons (ATOP) [ Time Frame: baseline, 3 weeks ]Self-reported measure about a person's attitudes towards obese persons to see whether their attitude towards people living with obesity changed as a result of the knowledge gained through the obesity management workshop.
- Changes in Beliefs About Obese Persons (BAOP) [ Time Frame: baseline, 3 weeks ]Self-reported measure about a person's beliefs about obese persons to see whether their beliefs about people living with obesity changed as a result of the knowledge gained through the obesity management workshop.
- Changes in Self-Reported Comfort Level (Pre- and Post- Assessment Scale) [ Time Frame: baseline, 3 weeks ]The pre- and post- questionnaire is a self-reported measure of the resident's comfort level around each of the 5 areas of the 5A's Obesity Management. Questions related to each element of the 5A's are rated using a 5 point Likert Scale.
- Qualitative: Narrative Reflections [ Time Frame: baseline, 3 weeks ]Personal reflection on how the experience and the workshop made the person feel. These will be analyzed using qualitative analysis to see how the workshop may have affected views, beliefs and their practice.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02648308
|University of Alberta - Department of Family Medicine|
|Edmonton, Alberta, Canada|
|Principal Investigator:||Denise L Campbell-Scherer, MD, PhD||University of Alberta, Department of Family Medicine|
|Principal Investigator:||Arya Sharma||University of Alberta, Faculty of Medicine|