Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06997822

Integrated Recovery Program for Critical Illness

Led by National Taiwan University Hospital · Updated on 2025-12-03

240

Participants Needed

1

Research Sites

164 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to investigate the effects of the Integrated Critical Illness Aftercare and Recovery Enhancement (I-CARE) program on reducing healthcare burden and improving functional outcomes in ICU survivors. The I-CARE program combines remote support via LINE Bot Care with in-person post-ICU recovery clinic visits. The study will assess whether this integrated care model reduces unplanned hospital readmissions and emergency department visits within six months after discharge, and improves physical and cognitive outcomes at 3 and 6 months post-discharge. Additionally, the study will evaluate the impact of a built-in patient-nurse interaction feature on ICU nurses' burnout and intention to leave, measured every six months over a two-year period.

CONDITIONS

Official Title

Integrated Recovery Program for Critical Illness

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • ICU survivors who had experienced endotracheal intubation and mechanical ventilation treatment.
Not Eligible

You will not qualify if you...

  • ICU survivors who are unable to walk independently before admission
  • ICU survivors who are unable to receive assessment (e.g., dementia or mental retardation)
  • ICU survivors who don't have a smartphone.
  • ICU survivors were discharged to institutional care facilities

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

National Taiwan University Hospital

Taipei, Taiwan, 10055

Actively Recruiting

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Research Team

C

Cheryl Chia-Hui Chen, PhD

CONTACT

K

Kuo-Jen Hsu, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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Integrated Recovery Program for Critical Illness | DecenTrialz