Stress Management and Resiliency Training for Physicians
1 other identifier
interventional
160
1 country
2
Brief Summary
This study is to evaluate the effects of the SMART-3RP (Stress Management and Resiliency Training Relaxation Response Resiliency Program) on physician and academic faculty well-being, perceived stress, burnout, compassion, and job satisfaction.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jul 2018
Typical duration for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 18, 2018
CompletedFirst Posted
Study publicly available on registry
June 27, 2018
CompletedStudy Start
First participant enrolled
July 9, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2021
CompletedFebruary 24, 2021
February 1, 2021
3 years
June 18, 2018
February 22, 2021
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in perceived stress: pre-program vs. post-program
Change in score on the perceived stress scale - 10 item instrument (PSS-10) from baseline to completion of the group.
Approximately 2 months
Study Arms (2)
Intervention
EXPERIMENTALParticipants will receive the 8-week SMART-3RP intervention within a few weeks of enrolling in the study.
No Intervention
NO INTERVENTIONParticipants will not receive the SMART-3RP program and will only complete study questionnaires..
Interventions
This is an 8-week, multimodal resiliency program that targets stress with 4 main components: mind-body skills (participants learn a variety of meditation techniques, mini relaxations, walking meditation, and yoga), traditional stress management techniques, healthy lifestyle behaviors (sleep, exercise, nutrition, and social support), and cognitive reappraisal and adaptive coping skills (borrowed from cognitive behavioral therapy, acceptance and commitment therapy, and positive psychology). The program consists of 8, 1.5 hour sessions.
Eligibility Criteria
You may qualify if:
- Physicians and academic faculty of Brigham and Women's Hospital and Newton-Wellesley Hospital
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Brigham and Women's Hospital
Boston, Massachusetts, 02115, United States
Newton Wellesley Hospital
Newton, Massachusetts, 02462, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
John Denninger, MD, PhD
Benson-Henry Institute for Mind Body Medicine
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Director of Research
Study Record Dates
First Submitted
June 18, 2018
First Posted
June 27, 2018
Study Start
July 9, 2018
Primary Completion
June 30, 2021
Study Completion
June 30, 2021
Last Updated
February 24, 2021
Record last verified: 2021-02
Data Sharing
- IPD Sharing
- Will not share