Evaluation of Mind-body Educational Program to Enhance Resiliency and Reduce Burnout in First Year Residents
Primary Purpose
Stress
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Stress Management and Resiliency Training for Residents (SMART-R)
Sponsored by
About this trial
This is an interventional treatment trial for Stress focused on measuring mind/body medicine, 3RP, stress management, resident burnout
Eligibility Criteria
Inclusion Criteria:
- Massachusetts General Hospital first year resident in Department of Medicine or Department of Psychiatry
- 21 years of age or older
- consenting to participate in 3RP-1
Exclusion Criteria:
-
Sites / Locations
- MGH department of medicine and department of psychiatry
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
First Year Residents
Arm Description
Stress Management and Resiliency Training for Residents (SMART-R) delivered to first year residents in the departments of medicine and psychiatry at Massachusetts General Hospital
Outcomes
Primary Outcome Measures
Change in burnout levels post intervention
Maslach Burnout Inventory (MBI), a validated 22-item self-report measure of professional burnout in human services. The MBI consists of 3 subscales of burnout: emotional exhaustion, depersonalization, and low sense of personal accomplishment.
Change in perceived stress post intervention
Perceived Stress Scale (PSS-10)
Change in continuous physiologic data throughout intervention
Basis Peak Health Tracking device collects continuous physiologic data (heart rate, galvanized skin response, sleep duration and quality, exercise and actigraphy)
change in coping abilities post intervention
Measure of Coping Status-Revised (MOCS-R)
Secondary Outcome Measures
change in self-reported anxiety and depression
Beck Anxiety Inventory (BAI) and Patient Health Questionnaire 9-item
Full Information
NCT ID
NCT02621788
First Posted
May 14, 2015
Last Updated
December 1, 2015
Sponsor
Massachusetts General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02621788
Brief Title
Evaluation of Mind-body Educational Program to Enhance Resiliency and Reduce Burnout in First Year Residents
Official Title
Evaluation of Mind-body Educational Program to Enhance Resiliency and Reduce Burnout in First Year Residents
Study Type
Interventional
2. Study Status
Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
April 2014 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
July 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This prospective pilot study evaluated the benefits of a stress management and resiliency training program for residents (SMART-R).
The primary objective of this study is to determine whether the SMART-R effectively reduces burnout and stress and enhances coping skills in first year residents. Objective parameters (heart rate, galvanized skin response, sleep duration and quality, exercise and actigraphy) measured with the Basis health tracking device will help correlate objective signs to subjective report of stress.
The investigators' hypothesis is that the SMART-R, a curriculum designed to teach first year residents (in the department of Medicine and Psychiatry) relaxation skills, will enhance residents' emotional and physical well being, reduce reports of stress, anxiety, depression, and physical complaints, as well as increase overall resiliency.
Detailed Description
The SMART-R has been developed by the Benson-Henry Institute (BHI) of Mind Body Medicine and is aimed at reducing the impact of stress through a variety of skill building exercises. The exercises incorporated into the program have been shown to improve physical symptoms, mood and wellbeing in medical patient populations. However, very little work has focused on healthcare providers, and there are no studies that look at mindfulness interventions for resident physicians specifically.
Participants enrolled will be invited to complete a set of questionnaire before and after participation in the program. The investigators will also collect continuous physiologic data using the Basis Peak Health Tracking device to correlate the physiologic data with self-report measures of stress.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stress
Keywords
mind/body medicine, 3RP, stress management, resident burnout
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
85 (Actual)
8. Arms, Groups, and Interventions
Arm Title
First Year Residents
Arm Type
Experimental
Arm Description
Stress Management and Resiliency Training for Residents (SMART-R) delivered to first year residents in the departments of medicine and psychiatry at Massachusetts General Hospital
Intervention Type
Behavioral
Intervention Name(s)
Stress Management and Resiliency Training for Residents (SMART-R)
Intervention Description
The SMART-R is a mind-body Educational Program for residents that is aimed at reducing the impact of stress and enhancing coping strategies through skill building exercises. The intervention consists of 3, 2 hour sessions over the course of 12 months.
Primary Outcome Measure Information:
Title
Change in burnout levels post intervention
Description
Maslach Burnout Inventory (MBI), a validated 22-item self-report measure of professional burnout in human services. The MBI consists of 3 subscales of burnout: emotional exhaustion, depersonalization, and low sense of personal accomplishment.
Time Frame
change between baseline (week 0) and post intervention (week 52)
Title
Change in perceived stress post intervention
Description
Perceived Stress Scale (PSS-10)
Time Frame
change between baseline (week 0) and post intervention (week 52)
Title
Change in continuous physiologic data throughout intervention
Description
Basis Peak Health Tracking device collects continuous physiologic data (heart rate, galvanized skin response, sleep duration and quality, exercise and actigraphy)
Time Frame
change between baseline (week 0) and post intervention (week 52)
Title
change in coping abilities post intervention
Description
Measure of Coping Status-Revised (MOCS-R)
Time Frame
change between baseline (week 0) and post intervention (week 52)
Secondary Outcome Measure Information:
Title
change in self-reported anxiety and depression
Description
Beck Anxiety Inventory (BAI) and Patient Health Questionnaire 9-item
Time Frame
change between baseline (week 0) and post intervention (week 52)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Massachusetts General Hospital first year resident in Department of Medicine or Department of Psychiatry
21 years of age or older
consenting to participate in 3RP-1
Exclusion Criteria:
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Denninger, M.D./PhD
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
MGH department of medicine and department of psychiatry
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Evaluation of Mind-body Educational Program to Enhance Resiliency and Reduce Burnout in First Year Residents
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