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Reliability and validity analysis of the China Nanjing Consciousness Recovery Scale —a multi-center study

Reliability and validity analysis of the China Nanjing Consciousness Recovery Scale —a multi-center study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400094107
Enrollment
Unknown
Registered
2024-12-17
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

disorders of consciousness

Interventions

Trail group:no

Sponsors

Nanjing Zijin Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients with brain injury admitted to each sub-center from January 1, 2025 due to various reasons: such as head injury, cerebral hemorrhage, cerebral infarction, hypoxic ischemic encephalopathy, CO poisoning, encephalitis, etc.; 2. Aged from 0 to 80; 3. Gender is not limited; 4. Consciousness state ranges from coma to consciousness; 5. Disease course within 12 months; 6. The patient himself or his guardian voluntarily participates in the study and signs the informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of mental retardation; 2. Those who have suffered severe brain damage in the past and have residual effects; 3. History of severe mental illness; 4. Patients with status epilepticus, refractory epilepsy, and long-term use of large amounts of antiepileptic drugs; 5.Individuals who have received sedatives, psychostimulants, or muscle relaxants within 48 hours prior to the assessment of the scale; 6. The patient or guardian did not sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Glasgow Coma Scale, GCS;Coma Recovery Scale, CRS-R;China Nanjing Consciousness Recovery Scale, CNCRS;reliability;validity;

Countries

China

Contacts

Public ContactJiangping Ge

Nanjing Zijin Hospital

602134618@qq.com+86 137 0516 8086

Outcome results

None listed

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