The Reliability and Validity of Perioperative Cognitive Test Network Platform for Monitoring Neurocognitive Changes

Air Force Military Medical University of People's Liberation Army

Status: Not yet enrolling

Conditions: Perioperative Neurocognitive Disorders

Study type: Observational

Funder types: Other

Identifiers

NCT06028568

KY20232188-C-1

Details and patient eligibility

About

This study aimed to analyze the reliability and validity of the results of the new designed perioperative cognitive test network platform, and to judge the reliability and scientific nature of the perioperative cognitive test. And then to explore whether the perioperative cognitive test network platform can be used to evaluate the changes of perioperative cognitive function of patients.

Full description

Two cohorts of elderly healthy volunteers and elderly patients undergoing abdominal surgery will be included in this study. The cognitive function of the patients was tested one day before and seven days after operation. Healthy volunteers had two cognitive function tests at the same interval. The normality test is used to evaluate whether the test results accord with the normal distribution. The internal consistency of the test was evaluated by calculating the Cronbach coefficient, the content validity was evaluated by experts and the content validity index was calculated, and the construct validity of the test was evaluated by exploratory factor analysis and confirmatory factor analysis. The validity of the test was evaluated by calculating the effect scale.

Enrollment: 400 estimated patients

Sex: All

Ages: 65+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Age over 65
• Scheduled for abdominal surgery under general anesthesia (grade 3-4 surgery based on surgical grade)
• Informed consent has been obtained
• Healthy volunteer groups are listed as age-and sex-matched community groups

Exclusion criteria

• Unable to follow instruction and finish the firtst procedure
• Has severe visual or auditory problems
• History of drug or alcohol abuse (drinking more than 5U daily in the past 3 months, 1U equals 10ml or 8g pure alcohol, equivalent to >50 liquor over 100ml, two two
• Are diagnosed neuropsychological disease that needs treatment
• Clear history of severe cerebrovascular diseases (including cerebral hemorrhage and cerebral infarction), Parkinson's syndrome, schizophrenia, bipolar disorder, depression, dementia, Alzheimer's disease, etc
• Severe head trauma, carbon monoxide poisoning and other loss of consciousness more than 30 minutes
• MMSE score ≤23
• Participated this study or being participating other clinical research

Trial design

400 participants in 2 patient groups

Elderly patients undergoing surgery

Description:

Older than or equal to 65 years of age; patients who intend to undergo major abdominal surgery under general anesthesia (grade 3-4 surgery based on surgical grade)

Elderly healthy volunteers

Description:

Age-and sex-matched community population