ClinicalTrials.Veeva

Menu

Outcome Prediction in Patients With Acute Disorders of Consciousness

Zhejiang University logo

Zhejiang University

Status

Enrolling

Conditions

Consciousness Disorder

Treatments

Device: Electric stimulation device(Neuroconn)

Study type

Observational

Funder types

Other

Identifiers

NCT04411719
Outcome in DOC

Details and patient eligibility

About

Prior research has indicated a link between outcomes in patients with disorders of consciousness (DOC) and their responses to emotional auditory stimuli. Given the high degree of uncertainty in acute situations, this study plans to record EEG responses and observe microexpressions in DOC patients during exposure to auditory stimuli, with the aim to identify more reliable prognostic indicators. The goal is to uncover potential patterns or signals that can contribute to a more comprehensive understanding of a patient's condition, and thereby provide more accurate prognostication.

Full description

This study intends to probe the potential of electroencephalography (EEG) and microexpression analysis for predicting the outcomes of acutely unresponsive patients within the intensive care unit (ICU). Previous research has illuminated a relationship between patients' emotional responses to auditory stimuli and their prognosis. However, the predictive utility of these responses in the context of acute conditions remains largely unexplored.

At the onset of the study, participants will undergo EEG monitoring while exposed to a pre-determined set of emotional auditory stimuli. Additionally, the patients' facial expressions will be captured via video for subsequent microexpression analysis.

Follow-up assessments of the patients' status will be conducted at three, six, and twelve-month intervals. Using cutting-edge analytical techniques, the goal is to decode these EEG and microexpression responses. This study aims to identify possible correlations between these findings, the patients' diagnoses, and their respective outcomes over time.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with acute brain injury (<28 days) in ICU
  • GCS ≤ 8
  • ≥ 2 days after sedation
  • Normal hearing, with auditory startle reflex

Exclusion criteria

• Children under 18

Trial design

60 participants in 1 patient group

EEG and Microexpression Analysis
Description:
Participants will be acutely unresponsive ICU patients. They will undergo non-invasive observational procedures, including EEG monitoring during exposure to emotional auditory stimuli, and concurrent video recording for microexpression analysis. Patient outcomes will be assessed at three, six, and twelve-month intervals post-initial observation.

Trial contacts and locations

1

Loading...

Central trial contact

Benyan Luo, Prof

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems