Trials / Recruiting
RecruitingNCT06995742
Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity
Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity: A Randomized Controlled Trial
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 270 (estimated)
- Sponsor
- Northwestern University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Randomized controlled trial of a time motion study of time spent obtaining and charting vital signs for inpatients, comparing use of a wireless Bluetooth vital sign array as intervention versus routine vital sign obtainment activity on a general medical floor.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Device Array Use | Study participants assigned to the intervention study arm will wear a wireless Bluetooth capable vital sign detection array, with one device externally worn on each of their chest, one finger, and one arm, with healthcare providers using an additional oral temperature probe. |
| DEVICE | Routine Vital Sign Measurement | Study participants randomized to the control arm will have their vital signs obtained by routine means, without use of the wireless vital sign device array. |
Timeline
- Start date
- 2025-06-02
- Primary completion
- 2026-07-31
- Completion
- 2026-07-31
- First posted
- 2025-05-29
- Last updated
- 2025-06-05
Locations
2 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06995742. Inclusion in this directory is not an endorsement.