Actively Recruiting

Age: 18Years - 100Years
All Genders
Healthy Volunteers
NCT06427265

Machine Learning-based Longitudinal Study of Post-ICU Syndrome Development Trajectory in Critically Ill Patients and Construction of Clinical Early Warning Models: a Research Protocol for Longitudinal Study

Led by The Affiliated Hospital Of Guizhou Medical University · Updated on 2025-05-31

840

Participants Needed

1

Research Sites

130 weeks

Total Duration

On this page

Sponsors

T

The Affiliated Hospital Of Guizhou Medical University

Lead Sponsor

C

Chinese nursing association

Collaborating Sponsor

AI-Summary

What this Trial Is About

This project intends to track and evaluate whether post-ICU syndrome will occur 7 days, 1 month, 3 months and 6 months after ICU patients are transferred out of the ICU through a longitudinal study, apply the latent category growth model to identify different trajectory patterns of post-ICU syndrome in critically ill patients, and use modern machine learning models to build an early warning model of the trajectory patterns of post-ICU syndrome.

CONDITIONS

Official Title

Machine Learning-based Longitudinal Study of Post-ICU Syndrome Development Trajectory in Critically Ill Patients and Construction of Clinical Early Warning Models: a Research Protocol for Longitudinal Study

Who Can Participate

Age: 18Years - 100Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Stayed in ICU for 24 hours or more
  • Age 18 years or older
  • Conscious and able to communicate without barriers when leaving ICU
  • Provided informed consent
  • One family member aged 18 or older acts as primary caregiver and medical decision-maker
  • Family member has no history of mental illness or serious organic diseases
  • Family member provides informed consent and voluntarily participates
Not Eligible

You will not qualify if you...

  • ICU stay longer than 24 hours within 3 months before this admission
  • Transferred to another ICU
  • Cognitive impairment before ICU admission (BDRS > 4 points)
  • Severe hearing impairment or speech difficulties preventing follow-up
  • Unable to complete questionnaires due to serious illness
  • Family members refuse to participate or have severe hearing or language impairments preventing cooperation

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

Affiliated Hospital of Guizhou Medical University

Guiyang, Guizhou, China, 550004

Actively Recruiting

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Research Team

T

Tingrui WANG

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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