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Clinical Trials/NCT02621788
NCT02621788
Completed
Not Applicable

Evaluation of Mind-body Educational Program to Enhance Resiliency and Reduce Burnout in First Year Residents

Massachusetts General Hospital1 site in 1 country85 target enrollmentApril 2014
ConditionsStress

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stress
Sponsor
Massachusetts General Hospital
Enrollment
85
Locations
1
Primary Endpoint
Change in continuous physiologic data throughout intervention
Status
Completed
Last Updated
10 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
April 2014
End Date
July 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

John W. Denninger, MD, PhD

Director of Research

Massachusetts General Hospital

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

  • Not provided

Outcomes

Primary Outcomes

Change in continuous physiologic data throughout intervention

Time Frame: change between baseline (week 0) and post intervention (week 52)

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

Time Frame: change between baseline (week 0) and post intervention (week 52)

Measure of Coping Status-Revised (MOCS-R)

Change in burnout levels post intervention

Time Frame: change between baseline (week 0) and post intervention (week 52)

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

Time Frame: change between baseline (week 0) and post intervention (week 52)

Perceived Stress Scale (PSS-10)

Secondary Outcomes

  • change in self-reported anxiety and depression(change between baseline (week 0) and post intervention (week 52))

Study Sites (1)

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