- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07406074
Duke Virtual IntEgrated Workflow (Duke VIEW)
February 9, 2026 updated by: Duke University
DUH Innovation Units
This quality improvement initiative aims to evaluate the implementation, utilization, and impact of virtual care technologies and workflows being implemented at Duke University Health System (DUHS).
This project is embedded within operational workflows and is designed to inform strategic decision-making and resource allocation.
The evaluation will focus on key performance indicators (KPIs) relevant to hospital operations and patient outcomes, including but not limited to: Length of Stay, Readmission Rates, Patient Satisfaction Scores, and Other Quality and Safety Metrics.
These KPIs will be evaluated across three clinical units at Duke University Hospital, in which virtual care technologies are being implemented.
These will be compared to three control units of similar characteristics.
Differences in KPIs will be examined across all units over 12 months.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
10000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ryan Shaw, PhD
- Phone Number: 9196849434
- Email: ryan.shaw@duke.edu
Study Contact Backup
- Name: Joanna Cavalier, MD
- Email: joanna.cavalier@duke.edu
Study Locations
-
-
North Carolina
-
Durham, North Carolina, United States, 27710
- Duke University Hospital
-
Contact:
- Ryan Shaw, PhD
- Phone Number: 919-684-9434
- Email: ryan.shaw@duke.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients admitted to medical surgical floors
Description
Inclusion Criteria:
- Admission to the hospital on one of six clinical units
Exclusion Criteria:
- Less than 18 years old
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Clinical Unit 1
All patient beds on clinical unit 1
|
Patient care delivered together with a bedside nurse and a virtual nurse
|
|
Clinical Unit 2
All patient beds on clinical unit 2
|
Patient care delivered together with a bedside nurse and a virtual nurse
|
|
Clinical Unit 3
All patient beds on clinical unit 3
|
Patient care delivered together with a bedside nurse and a virtual nurse
|
|
Clinical Unit 4
All patient beds on clinical unit 4
|
|
|
Clinical Unit 5
All patient beds on clinical unit 5
|
|
|
Clinical Unit 6
All patient beds on clinical unit 6
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Falls
Time Frame: 12 months
|
Number of patient falls in a hospital room
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Readmission rates
Time Frame: 12 months
|
Rate of readmission to the hospital after discharge
|
12 months
|
|
Central Line-Associated Bloodstream Infection
Time Frame: 12 months
|
Number of Central Line-Associated Bloodstream Infections
|
12 months
|
|
Hospital acquired pressure injury
Time Frame: 12 months
|
Number of hospital acquired pressure injuries
|
12 months
|
|
Venous thromboembolism
Time Frame: 12 months
|
Number of venous thromboembolisms
|
12 months
|
|
Nurse Turnover
Time Frame: 12 months
|
Rate of nurse turnover over time
|
12 months
|
|
Patient Satisfaction Questionnaire (PSQ-18)
Time Frame: 12 months
|
The PSQ is an 18-item survey designed for quick assessment of patient satisfaction with healthcare.
Each item is scored on a Likert scale of 1 to 5 and has a total score range of 18 to 90, where a higher score indicates greater satisfaction.
|
12 months
|
|
Length of Stay
Time Frame: 12 months
|
Average length of stay
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ryan Shaw, PhD, Duke Health
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
February 4, 2026
Primary Completion (Estimated)
February 3, 2027
Study Completion (Estimated)
February 3, 2027
Study Registration Dates
First Submitted
February 3, 2026
First Submitted That Met QC Criteria
February 9, 2026
First Posted (Actual)
February 12, 2026
Study Record Updates
Last Update Posted (Actual)
February 12, 2026
Last Update Submitted That Met QC Criteria
February 9, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- Pro00118673
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
Study outcome measures will be shared
IPD Sharing Time Frame
IPD and supporting information will be available within three years of study completion and hosted at Duke University in the Duke Research Data Repository
IPD Sharing Access Criteria
Data will be made available publicly in accordance with the Duke Research Data Repository
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ANALYTIC_CODE
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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