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Impact of a Wearable Fitness Tracker on Otolaryngologists' Burnout

Wake Forest University (WFU) logo

Wake Forest University (WFU)

Status

Withdrawn

Conditions

Burnout
Wellness
Sleep Deprivation
Stress

Treatments

Behavioral: WHOOP fitness tracker

Study type

Interventional

Funder types

Other

Identifiers

NCT04738747
IRB00070943

Details and patient eligibility

About

Study the impact of the WHOOP fitness tracker on burnout in attending and resident otolaryngologists

Full description

The study will be a randomized controlled trial of attending and resident otolaryngologists who will be randomized to either wearing a WHOOP fitness tracker or a control group. Participants will take two Maslach burnout inventory (MBI) surveys prior to the start of the intervention to set a baseline burnout score, and then at 3 months and 6 months into the study. Baseline cardiac status will also be established by taking a pre-intervention heart rate and blood pressure.

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All attending and resident Otolaryngologists at Wake Forest Baptist Health

Exclusion criteria

  • Users of a WHOOP device currently
  • Current interns will be excluded given they do not work with the Otolaryngology team the whole year

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Study arm (receive a WHOOP device)
Experimental group
Description:
Participants randomized to the WHOOP group will be given WHOOP wrist and arm bands to wear 24/7 after an orientation on their use
Treatment:
Behavioral: WHOOP fitness tracker
Control arm (no intervention)
No Intervention group
Description:
The control group will not have any intervention

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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