Impact of a Wearable Fitness Tracker on Otolaryngologists' Burnout

Sponsor
Wake Forest University Health Sciences (Other)
Overall Status
Withdrawn
CT.gov ID
NCT04738747
Collaborator
(none)
0
2
7.1

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Behavioral: WHOOP fitness tracker
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Study the impact of the WHOOP fitness trackerStudy the impact of the WHOOP fitness tracker
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Impact of a Wearable Fitness Tracker on Otolaryngologists' Burnout
Anticipated Study Start Date :
Jul 1, 2021
Anticipated Primary Completion Date :
Jan 1, 2022
Anticipated Study Completion Date :
Feb 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Study arm (receive a WHOOP device)

Participants randomized to the WHOOP group will be given WHOOP wrist and arm bands to wear 24/7 after an orientation on their use

Behavioral: WHOOP fitness tracker
WHOOP is a device that uses a wristband or arm band to track heart rate, heart rate variability (HRV), and sleep to calculate proprietary strain and recovery scores for its users. Heart rate variability is an important metric for correlation with acute stress

No Intervention: Control arm (no intervention)

The control group will not have any intervention

Outcome Measures

Primary Outcome Measures

  1. Change in Maslach Burnout Inventory (MBI) Scores - emotional exhaustion [Baseline through Month 6]

    MBI items are scored using a 7 level frequency ratings from "never" to "daily" - emotional exhaustion (9 items) - Higher scores indicate higher burnout (worse) than lower scores (better)

  2. Change in Maslach Burnout Inventory (MBI) Scores - emotional exhaustion [Baseline through Month 3]

    MBI items are scored using a 7 level frequency ratings from "never" to "daily" - emotional exhaustion (9 items) - Higher scores indicate higher burnout (worse) than lower scores (better)

  3. Change in Maslach Burnout Inventory (MBI) Scores - depersonalization [Baseline through Month 3]

    MBI items are scored using a 7 level frequency ratings from "never" to "daily" - depersonalization (5 items) - Higher scores indicate higher burnout (worse) than lower scores (better)

  4. Change in Maslach Burnout Inventory (MBI) Scores - depersonalization [Baseline through Month 6]

    MBI items are scored using a 7 level frequency ratings from "never" to "daily" - depersonalization (5 items) - Higher scores indicate higher burnout (worse) than lower scores (better)

  5. Change in Maslach Burnout Inventory (MBI) Scores - personal achievement [Baseline through Month 3]

    MBI items are scored using a 7 level frequency ratings from "never" to "daily" - personal achievement (8 items) - Higher scores indicate higher burnout (worse) than lower scores (better)

  6. Change in Maslach Burnout Inventory (MBI) Scores - personal achievement [Baseline through Month 6]

    MBI items are scored using a 7 level frequency ratings from "never" to "daily" - personal achievement (8 items) - Higher scores indicate higher burnout (worse) than lower scores (better)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Wake Forest University Health Sciences

Investigators

  • Principal Investigator: Lyndsay Madden, DO, Wake Forest Health Sciences

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Wake Forest University Health Sciences
ClinicalTrials.gov Identifier:
NCT04738747
Other Study ID Numbers:
  • IRB00070943
First Posted:
Feb 4, 2021
Last Update Posted:
Aug 2, 2021
Last Verified:
Jan 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Wake Forest University Health Sciences
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2021