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Recruiting NCT06997822

NCT06997822 Integrated Recovery Program for Critical Illness

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Clinical Trial Summary
NCT ID NCT06997822
Status Recruiting
Phase —
Sponsor National Taiwan University Hospital
Condition ICU Survivors
Study Type INTERVENTIONAL
Enrollment 240 participants
Start Date 2025-11-03
Primary Completion 2028-07-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
LINE Bot-Based Remote Care Combined with In-Person Post-ICU Clinic

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 240 participants in total. It began in 2025-11-03 with a primary completion date of 2028-07-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

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 retardation) * ICU survivors who don't have a smartphone. * ICU survivors were discharged to institutional care facilities

Contact & Investigator

Central Contact

Cheryl Chia-Hui Chen, PhD

✉ cherylchen@ntu.edu.tw

📞 (886) 2-23123456

Frequently Asked Questions

Who can join the NCT06997822 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying ICU Survivors. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06997822 currently recruiting?

Yes, NCT06997822 is actively recruiting participants. Contact the research team at cherylchen@ntu.edu.tw for enrollment information.

Where is the NCT06997822 trial being conducted?

This trial is being conducted at Taipei, Taiwan.

Who is sponsoring the NCT06997822 clinical trial?

NCT06997822 is sponsored by National Taiwan University Hospital. The trial plans to enroll 240 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology