Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity

Part of paid clinical trials in Chicago, Illinois.

Sponsor
Northwestern University
Study ID
NCT06995742
Status
Recruiting
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Conditions

  • Patient Satisfaction
  • Provider Behavior
  • Sleep Quality
  • Vital Sign Evaluation
  • Vital Sign Monitoring

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Device Array Use — DEVICE
    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.
  • Routine Vital Sign Measurement — DEVICE
    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.

Study Details

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.

Key Dates

Start date
Jun 2, 2025
Status verified
Jun 2025
Primary completion
Jul 31, 2026
Completion
Jul 31, 2026

Study Design

Enrollment
270 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH

Arms

  • Experimental: Intervention--Device Array Use
    Inpatients will wear the ANNE One device array for obtainment of vital sign assessments.
  • Active Comparator: Control--Routine Vital Sign Obtainment
    Inpatients will have vital signs determined by routine practice, using any other standard of care-accepted method or device.

Primary Outcome Measure

Time Motion Assessment of Time Spent Obtaining and Recording Vital Signs [ Time Frame: Number of seconds spent obtaining and charting vital signs is obtained at 8a daily, for maximum of three days for each study participant, and are added together to equal the total time spent on vital sign assessment. ]

Central Contacts

Locations (2)

FacilityCityStateZIPSite coordinators
Feinberg 16 West, Northwestern Memorial HospitalChicagoIllinois60611
Gregory R Smith Jr, MD MS
[email protected]
312-926-5893
Gregory R Smith Jr, MD MS (PRINCIPAL_INVESTIGATOR)
Northwestern Memorial HospitalChicagoIllinois60611
Gregory (Randy) R Smith Jr, MD MS
[email protected]
312-926-5893

Find similar trials in Chicago, IL

By research site
Feinberg 16 West, Northwestern Memorial Hospital· Chicago, ILNorthwestern Memorial Hospital· Chicago, IL

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