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Mayo Clinic Family Medicine Resident Wellness Study

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Mayo Clinic

Status

Completed

Conditions

Sleep Patterns

Treatments

Other: Actigraph and activPAL devices
Other: Questionnaires

Study type

Interventional

Funder types

Other

Identifiers

NCT05148221
21-007624

Details and patient eligibility

About

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.

Full 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.

Enrollment

13 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

13 participants in 1 patient group

A three-week tailored, virtual exercise intervention.
Experimental group
Description:
A three-week tailored, virtual exercise intervention.
Treatment:
Other: Questionnaires
Other: Actigraph and activPAL devices

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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