Integrated Recovery Program for Critical Illness
Recruiting
N/A
Interventional Study
ICU Survivors
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 240 (estimated)
- Sponsor
- National Taiwan University Hospital · Other
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About This Trial
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 hosp…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* ICU survivors who had experienced endotracheal intubation and mechanical ventilation treatment.
Exclusion Criteria:
* ICU survivors who are unable to walk independently before admission
* ICU survivors who are unable to receive assessment (e.g., dementia or mental retardatio…
Contacts