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Clinical Trials/NCT02621801
NCT02621801
Unknown
Not Applicable

Evaluation of a Mind-body Education Program to Enhance Resiliency and Reduce Burnout in Residents

Massachusetts General Hospital1 site in 1 country173 target enrollmentAugust 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Resident Burnout
Sponsor
Massachusetts General Hospital
Enrollment
173
Locations
1
Primary Endpoint
Change in burnout levels post intervention
Last Updated
10 years ago

Overview

Brief Summary

This prospective, waitlist-control study is evaluating the benefits of a stress management and resiliency training program for residents (SMART-R).

The primary aim of this study is to determine whether the SMART-R is effective at increasing coping skills and reducing stress among residents, reflected by changes in constructs such as emotional growth, perceived stress, optimism, and coping styles. 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.

Detailed Description

The investigators adapted the Benson-Henry Institute Stress Management and Resiliency Training Program -- Relaxation Response Resiliency Program (SMART-3RP) to create the SMART-R resident wellness curriculum. The actual SMART-3RP is both a clinical program and research intervention. The three prongs of the SMART-R include 1) elicitation of the relaxation response through mind-body techniques 2) reducing overall stress reactivity and 3) increasing connectedness to self and others. In a waitlist-control design, the SMART-R was implemented into multiple residents programs at Mass General Hospital, NYU Langone Medical Center, and Weill Cornell Medical College. The primary aim is to evaluate the effectiveness of the SMART-R in increasing coping skills and reducing stress among residents in the participating programs. Participants enrolled will be invited to complete 1) a brief questionnaire before, during (q3months) and after participation in the program (5 questionnaires total). 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. Additionally, objective indicators of daily workload (page frequency, and quantity of notes authored by a resident during a given period) will help control for residents' schedules and busyness, in evaluating perceived stress, wellbeing and other outcomes.

Registry
clinicaltrials.gov
Start Date
August 2015
End Date
July 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

John W. Denninger, MD, PhD

Principle Investigator

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Residents in the following participating departments: departments of psychiatry, pediatrics, or neurology at MGH, medicine or psychiatry at NYU, or medicine or psychiatry at Cornell

Exclusion Criteria

  • Not a resident in the participating departments

Outcomes

Primary Outcomes

Change in burnout levels post intervention

Time Frame: change between baseline (July 2015), midpoint (week 25), to 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.

Secondary Outcomes

  • Change in perceived stress post intervention(change between baseline (July 2015), midpoint (week 25), to post intervention (week 52))
  • Change in continuous physiologic data throughout intervention(change between baseline (July 2015), midpoint (week 25), to post intervention (week 52))
  • change in mindfulness post intervention(change between baseline (July 2015), midpoint (week 25), to post intervention (week 52))

Study Sites (1)

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