Viewing Study NCT02621801



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Last Modification Date: 2024-10-26 @ 11:53 AM
Study NCT ID: NCT02621801
Status: UNKNOWN
Last Update Posted: 2015-12-04
First Post: 2015-11-23

Brief Title: Evaluation of a Mind-body Education Program to Enhance Resiliency and Reduce Burnout in Residents
Sponsor: Massachusetts General Hospital
Organization: Massachusetts General Hospital

Study Overview

Official Title: Evaluation of a Mind-body Education Program to Enhance Resiliency and Reduce Burnout in Residents
Status: UNKNOWN
Status Verified Date: 2015-12
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
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

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None