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Mizzou Nurse Workload and Well-Being Study

University of Missouri (MU) logo

University of Missouri (MU)

Status

Invitation-only

Conditions

Nursing Workload
Burnout, Healthcare Workers

Treatments

Other: Multimethod data collection

Study type

Observational

Funder types

Other

Identifiers

NCT07247708
2101866
URC-025-19 (Other Grant/Funding Number)

Details and patient eligibility

About

This observational study will evaluate the feasibility of linking nursing workload to burnout and physiological well-being among acute care nurses. Researchers will collect data from three sources: hospital workforce management software, wearable health devices (Oura Rings), and validated surveys. Fifty nurses from intensive care and medical-surgical units at a level one trauma center will participate. The study will also include interviews to better understand workplace stressors. Findings will help identify patterns that contribute to burnout and guide the development of future interventions to support nurse well-being and improve workforce retention.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • RN participants must be at least 18 years of age.
  • Must be a credentialed registered nurse (RN) working fulltime (≥0.75 FTE) in the MUHC University Hospital on the surgical or cardiac ICUs, surgical specialties, or the cardiovascular unit.
  • Must own a smart phone capable of supporting latest version of the Oura app with internet connectivity (Apple iOS15 and higher; Android 8.0 and higher with Google Play services) and Bluetooth 4.0.
  • Ability to wear an Oura ring daily, 7 days/ week (at least 22 hours/day), and adhere to study procedures.
  • Able to complete informed consenting procedures.

Exclusion criteria

  • Known allergy or sensitivity to components of Oura ring.
  • RNs working part-time or per diem
  • Travel nurses
  • Known allergies to the Oura ring
  • Ring finger sizes incompatible with Oura Ring Gen 3 sizes

Trial design

50 participants in 2 patient groups

Intensive Care Unit
Description:
surgical ICU and cardiac ICU RNs
Treatment:
Other: Multimethod data collection
Medical-Surgical Unit
Description:
surgical and cardiovascular units
Treatment:
Other: Multimethod data collection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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