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Clinical Trials/NCT05148221
NCT05148221
Completed
N/A

Mayo Clinic Family Medicine Resident Wellness Study: Feasibility of a Tailored Virtual Exercise Program and Its Impacts on Sleep Patterns and Subjective Mental Fatigue Among Family Medicine Residents: A Step Towards Prevention of Burnout in Early Career Physicians

Mayo Clinic1 site in 1 country13 target enrollmentNovember 1, 2021
ConditionsSleep Patterns

Overview

Phase
N/A
Intervention
Not specified
Conditions
Sleep Patterns
Sponsor
Mayo Clinic
Enrollment
13
Locations
1
Primary Endpoint
Work-related mental fatigue
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The objectives of this study are to better understand the association between sleep characteristics (sleep disruptions and deprivations) during overnight shifts and mental fatigue among medical residents, and to explore the feasibility of a virtual, tailored exercise program on sleep characteristics, subjective mental fatigue, and burnout level among residents in family medicine.

Detailed Description

The purpose of the proposed study is two-fold: 1) to better understand the association between sleep characteristics (sleep disruptions and deprivations) during overnight shifts and mental fatigue among medical residents; and 2) to explore the feasibility of a three-week tailored, virtual exercise program on sleep characteristics, subjective mental fatigue, and burnout level among residents in family medicine. It is hypothesized that: 1) the greater the number of average sleep disruptions, and the greater the sleep deprivation, the greater the acute mental fatigue during overnight shifts reported by the family medicine residents; 2) the number of average sleep disruptions and the magnitude of sleep deprivation are greater during overnight shifts than non-overnight shifts among family medicine residents; and 3) a three-week tailored virtual exercise program will significantly increase the amount of physical activity throughout the day and reduce the levels of mental fatigue and perceived burnout during overnight shifts.

Registry
clinicaltrials.gov
Start Date
November 1, 2021
End Date
July 15, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Terri Nordin

Principal Investigator

Mayo Clinic

Eligibility Criteria

Inclusion Criteria

  • A Family Medicine Resident at the Mayo Clinic Health System of Eau Claire in either the PGY-1 Year, PGY-2 Year, or PGY-2 Year (5 residents from each year).

Exclusion Criteria

  • Participant is not able to wear the devices for the assigned timeframe.
  • Any condition the investigator considers will prevent compliance with study instructions.

Outcomes

Primary Outcomes

Work-related mental fatigue

Time Frame: up to 4 weeks

Subjective work-related mental fatigue will be measured using the OFER 15 which has 15 items on a 7-point Likert scale ranging from 0 (strongly disagree) to 6 (strongly agree). The three subscales of OFER 15 include: chronic fatigue (items 1-5), acute fatigue (items 6-10), and inter-shift recovery (items 11-15) experienced in the past few months. Scores for each subscale range from 0-100. Higher scores indicate acute and chronic fatigue and greater inter-shift recovery.

Work-related burnout

Time Frame: up to 4 weeks

Levels of burnout will be assessed using the Maslach Burnout Inventory (MBI) which has 22 items on a 7-point Likert scale of 0 (never) to 6 (every day), consisting of three subscales of burnout: emotional exhaustion, depersonalization, and personal accomplishment. Low personal accomplishment scores, high emotional exhaustion scores, and high depersonalization scores suggest increased levels of burnout.

Secondary Outcomes

  • Sleep duration(up to 4 weeks)
  • Sleep disruptions(up to 4 weeks)
  • Horizontal shifts during sleep per night(up to 4 weeks)

Study Sites (1)

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