N/A
N=80
LA-CEAL 4.0: Wearable Sensor Project
Health Care Workforce Burn Out · Stress
Bottom Line
View on ClinicalTrials.gov: NCT06086028 ↗Enrolled (actual)
80
Serious AEs
—
Results posted
Oct 2025
Primary outcome: Primary: Percentage of Days in Concordance Comparing Immediate Information Period With Delayed Information Period — 0.49; 0.50 % of days concordant
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Wrist worn sensor (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Tulane University
- Primary completion
- May 2024
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Days in Concordance Comparing Immediate Information Period With Delayed Information Period |
0.49; 0.50 | — |
| SECONDARY Change in Burnout Score From Baseline to Follow-up (Pre/Post Sensor Data Collection) |
38.82; 35.54 | — |
Summary
The study seeks to explore the efficacy of biofeedback collected via a wrist worn sensor in helping healthcare workers self-manage symptoms of stress and burnout.
Eligibility Criteria
Inclusion Criteria
- Age >=18 years.
- Ability to understand and speak English.
- Staff at FQHC.
- Smartphone compatible with the Biostrap sensor and phone application.
- Attending work during the six week study period.
Exclusion Criteria
- Unable or unwilling to give informed consent.
- Disclosed pregnancy at the start of the study.
- Pace maker or other device regulation heart rate/rhythm.
- Previous diagnosis of atrial fibrillation.
Data sourced from ClinicalTrials.gov (NCT06086028). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.