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Intelligent Follow-up and Intervention on Core Symptoms of ICU Survivors

A specialized intelligent follow-up protocol for ICU survivors: Focusing on Core Symptom Management

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118265
Enrollment
Unknown
Registered
2026-02-03
Start date
2026-02-03
Completion date
Unknown
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-ICU syndrome

Interventions

intervention group:Remote follow-up interventions were implemented via the Intelligent Follow-up Information System
control group:Routine post-discharge follow-up

Sponsors

Central Hospital, Tianjin University /Tianjin Third Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Age >= 18 years; 2. ICU stay >= 24 hours; 3. survival time after ICU transfer >= 7 days; 4. presence of at least one core symptom; 5. informed consent and voluntary participation in the study

Exclusion criteria

Exclusion criteria: 1. Those who have serious impairment in understanding and communication and cannot express their thoughts through arbitrary means; 2. those who return to ICU within 48h after transfer out; 3. those who are discharged 72h after transfer; 4. Expected survival period is less than 6 months

Design outcomes

Primary

MeasureTime frame
Health-related quality of life;Post-intensive care syndrome score;Rates of Emergency Room Revisits and Hospital Readmissions;—

Secondary

MeasureTime frame
Readiness to Return-to-Work score;—

Countries

China

Contacts

Public ContactHuang Yanlin

Central Hospital, Tianjin University /Tianjin Third Central Hospital

huangyanlin@tju.edu.cn+86 136 6215 8930

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026