NCT04962204UnknownNot Applicable
Efficacy of Virtual Visitation in Intensive Care Unit During COVID-19 Pandemic: Randomized Controlled Trial
Seoul National University Hospital2 sites in 1 country100 target enrollmentStarted: July 6, 2021Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Enrollment
- 100
- Locations
- 2
- Primary Endpoint
- FS-ICU score from caregivers at discharge or 7 days after initiation of study enrolled
Study Overview
Brief Summary
The purpose of this study is to identify the efficacy of virtual visitation in Intensive Care Unit on patients and their caregivers during COVID-19 Pandemic.
Detailed Description
After being informed about the study, all patients who meet the eligibility requirements will be randomized in a 1:1 ratio to intervention group (Virtual visitation once a day) or Control group (Phone interviews once a day).
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Patients who are expected to stay in the intensive care unit for more than 48 hours
- •Patients with a RASS score of -2 or higher
Exclusion Criteria
- •Patients who discharge or die within 48 hours of admission to ICU
Outcomes
Primary Outcomes
FS-ICU score from caregivers at discharge or 7 days after initiation of study enrolled
Time Frame: 7 days
The FS-ICU survey score reflected the satisfaction degree of caregivers. The overall satisfaction score is derived from questions 1 through 24.
Secondary Outcomes
No secondary outcomes reported
Investigators
Seung-Young Oh
Clinical Assistant Profeessor
Seoul National University Hospital
Study Sites (2)
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