A study of the effects of different auditory stimuli on the near-infrared features of the brain in patients with disorders of consciousness

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500098995

Enrollment

Unknown

Registered

2025-03-17

Start date

2024-01-15

Completion date

Unknown

Last updated

2025-03-24

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

Conditions

disorder of consciousness

Interventions

Group A of Experiment:Auditory stimulus

Group B of Experiment:Auditory stimulus

Control group:Auditory stimulus

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: a. Age 18-80 years, gender; b. CRS-R Scale Scale; c. DOC duration 28 days; d. No skull defect or skull repair; e. Voluntary participation of family members and signing of informed consent;

Exclusion criteria

Exclusion criteria: Exclusion criteria: a. auditory impairment; b. continuous aggravation, active cerebral hemorrhage or intracranial hypertension is not controlled; c. severe heart, lung, liver, renal dysfunction or other serious physical diseases;

Design outcomes

Primary

Measure	Time frame
oxyhemoglobin;	—

Countries

China

Contacts

Public ContactLi Wei

Binzhou Medical University Affiliated Hospital

yishengliwei@163.com+86 152 6672 0333

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026