Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Device Array Use, Routine Vital Sign Measurement.
- Who it may be relevant to
- Registry conditions: Vital Sign Evaluation, Vital Sign Monitoring, Sleep Quality, Provider Behavior. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity: A Randomized Controlled Trial
Overview
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.
Interventions
- 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.
Primary outcome measures
- 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.]
Secondary outcome measures (3)
- Sleep Quality of Inpatient Study Participants [Time frame: Survey conducted 24-72 hours after enrolment.]
- Patient Satisfaction with Inpatient Sleep Quality [Time frame: Survey sent within a week of hospital discharge and collected within the subsequent thirty days.]
- Healthcare Provider Experience with the Vital Sign Device Array [Time frame: The electronic survey will be administered twice during the study. Each survey will take approximately ten minutes to complete.]
Eligibility criteria
Inclusion criteria
- Inpatients admitted to Northwestern Memorial Hospital, Feinberg Unit 16 West.
Exclusion criteria
- Primary language other than English, under isolation status, pregnant patients, prisoners, employees or students of the hospital or Northwestern University.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Health services research
Study locations
United States · 2 centers
- Feinberg 16 West, Northwestern Memorial Hospital — Chicago
- Northwestern Memorial Hospital — Chicago
Identifiers
NCT: NCT06995742 · STU00219340 · 2023 Dixon Translational Grant