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Reliability and Validity of the NCS (NCS-R)-Chinese Version

CompletedNot applicableNCT03494218
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

The aim of this study was to translate the NCS from English into Chinese and determine the validity of this Chinese version.

Study details

Official title
Reliability and Validity of the Nociception Coma Scale (-Revised)-Chinese Version
Conditions
  • Minimally Conscious State
  • Vegetative State
Interventions
  • Diagnostic test: Nociception Coma Scale (NCS)
Sponsor
Hangzhou Normal University
Start date
2017-10-28
Primary completion
2018-02-02
Sex
All
Age range
from 19 Years to 53 Years
Results posted
No results posted in this snapshot
Countries
China
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * age ≥ 18 years old; * no administration of neuromuscular blockers or sedation within the 24 hours of enrolment; * the presence of periods of eye opening (indicating wakefulness and rest cycles); * a diagnosis of VS or MCS, based on more than 4 times behavioral assessment performed using the Coma Recovery Scale-Revised within 2 weeks. Exclusion Criteria: * Coma; * documented history of prior brain injury; * psychiatric or neurologic illness; * neuromuscular blocking agents or sedative drugs administered within the prior 24 hours; * no documented history of a prior coma, critical illness or unstable medical condition; * upper limb contusions, fractures (based on the imaging examination) or flaccid paralysis (by using noxious stimuli to upper limbs, motor sub-scale scores \<1).

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03494218