Clinical trial Recruiting at 1 site Interventional Ages 19 and up

Smartphone-based rehabilitation after ICU discharge

Official title: Feasibility of a Digital Rehabilitation Platform in Patients After ICU Discharge

Run by Asan Medical Center · NCT07489092 · Data updated 2026-11-12

This project will try a smartphone app to deliver daily, individualized rehab for adults recovering from ICU-acquired weakness to help them regain strength and function.

Quick facts

Study typeInterventional
Ages19 Years and up
SexAll
Enrollment70 (estimated)
SponsorAsan Medical Center
Academic / other
Locations1 site (Seoul)
StatusRecruiting
StartedFebruary 2, 2026
Main results expectedDecember 31, 2026
Study endsDecember 31, 2026
Registry record updatedMarch 23, 2026
Trial IDNCT07489092 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 19 or older who were in the ICU for more than 48 hours, are medically stable at ICU discharge, own a smartphone, and can operate the digital platform are ideal candidates.

Probably not a fit

Patients with unstable medical conditions, severe cognitive impairment or communication barriers, formal contraindications to exercise, or inability to use a smartphone are unlikely to benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective multicenter cohort enrolls adults (≥19 years) discharged from the ICU after more than 48 hours at two tertiary hospitals in Seoul, South Korea. Participants receive individualized daily rehabilitation sessions (up to 30 minutes) delivered through the Tuntun Rehabilitation Assistant smartphone platform, with a researcher assisting during the first five sessions. Physical and cognitive function, mobility, quality of life, platform usage, and safety events are measured at baseline, two weeks, hospital discharge, and during follow-up. Approximately 70 participants will be recruited to determine feasibility, usability, and preliminary clinical signals.

Why it matters

Potential benefit: If successful, the platform could make tailored rehabilitation easier to access and speed recovery of physical and cognitive function after ICU discharge.

How similar studies have gone: Early pilots and tele-rehabilitation programs for post-ICU patients have shown promising feasibility and functional gains, but robust randomized evidence is still limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 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.

Exclusion Criteria:

* 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.

Where it's running

  • Asan Medical Center
    Seoul, South Korea
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.