Actively Recruiting
Feasibility of a Digital Rehabilitation Platform in Patients After ICU Discharge
Led by Asan Medical Center · Updated on 2026-03-23
70
Participants Needed
1
Research Sites
47 weeks
Total Duration
On this page
Sponsors
A
Asan Medical Center
Lead Sponsor
S
Seoul National University Bundang Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
This study aims to evaluate the feasibility, usability, and clinical effectiveness of a digital rehabilitation platform in adult patients discharged from the intensive care unit (ICU). Adult patients aged 19 years or older who stayed in the ICU for more than 48 hours and are capable of using a smartphone will be enrolled from two tertiary hospitals in South Korea. Participants will receive individualized rehabilitation programs using a digital rehabilitation platform ("Tuntun Rehabilitation Assistant") based on their functional status. Rehabilitation will be conducted once daily for up to 30 minutes per session. Physical and cognitive function outcomes will be assessed at baseline, two weeks after intervention initiation, at hospital discharge, and during follow-up when applicable. This prospective cohort study will investigate changes in physical function, mobility, cognitive status, and quality of life, as well as platform usage and safety-related events, to determine the clinical usefulness of digital rehabilitation for ICU survivors.
CONDITIONS
Official Title
Feasibility of a Digital Rehabilitation Platform in Patients After ICU Discharge
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 19 years or older
- Admission to the intensive care unit (ICU) for more than 48 hours
- Hospitalization at Asan Medical Center or Seoul National University Bundang Hospital
- Discharge from the ICU at the time of enrollment
- Ownership of a smartphone and ability to operate a digital rehabilitation platform
- Ability to understand the study procedures and provide voluntary written informed consent
You will not qualify if you...
- Medical conditions that contraindicate participation in rehabilitation exercise, as determined by the attending physician
- Severe cognitive impairment or communication difficulties that interfere with understanding or following study instructions
- Unstable medical conditions requiring ongoing intensive medical treatment
- Inability to use a smartphone or digital platform independently
- Refusal to participate or withdrawal of informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Asan Medical Center
Seoul, South Korea
Actively Recruiting
Research Team
W
Won Kim, Associate professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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