The Cognitive Protective Effect of VR-based Cognitive Training in Type 2 Diabetes Patients With Mild Cognitive Impairment

NCT ID
NCT07650318
Registry status
Recruiting
Study type
Not specified in the registry data
Phase
Not applicable
Sponsor
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School

Overview

ClinicalTrials.gov lists this study as Recruiting.

Enrollment: 40 participants (Estimated).

What is being studied

No interventions are listed in the registry data.

Who may be eligible

Ages
Not specified in the registry data
Sex
Not specified in the registry data
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: 1. Aged 45-80 years; gender is not restricted; 2. Participants must meet the diagnostic criteria for diabetes outlined in the \*Chinese Guidelines for the Prevention and Treatment of Type 2 Diabetes (2020 Edition)\*, namely: patients exhibit typical symptoms of diabetes and meet one of the following conditions: 1) HbA1c ≥ 6.5%; 2) Fasting blood glucose ≥7.0 mmol/L. Fasting is defined as no caloric intake for at least 8 hours; 3) 2-hour postprandial blood glucose ≥11.1 mmol/L following an oral glucose tolerance test; 4) Random blood glucose ≥11.1 mmol/L; 3. Stable glycemic control regimen for 3 months or longer; 4. Completed a systematic neuropsychological assessment and meets Petersen criteria for Mild Cognitive Impairment, satisfying the following conditions: 1) The patient or a caregiver subjectively perceives a decline in cognitive function; 2) Assessment results indicate impairment in one or more cognitive domains; 3) There is mild impairment in complex instrumental activities of daily living, but the patient maintains independence in basic activities of daily living; 4) Does not yet meet the diagnostic criteria for dementia; 5. Has an educational level of elementary school or higher and is able to cooperate in completing the assessment, VR training, and various examinations; 6. Cooperate in undergoing magnetic resonance imaging (MRI) examinations; 7. Voluntarily participates in this study, signs an informed consent form, and is able to comply with the study protocol requirements to complete follow-up. Exclusion Criteria: 1. Suffering from other dementia-related neurological disorders (such as Alzheimer's disease, Parkinson's disease, etc.) or severe mental illness; 2. History of central nervous system disorders, including traumatic brain injury, intracranial hemorrhage, acute cerebral infarction, etc.; 3. Severe sinusitis, space-occupying lesions in the nasopharynx, or congenital disorders affecting the sense of smell,or a history of trauma; 4. Glaucoma, severe dry eye syndrome, uncorrected strabismus, severe diabetic retinopathy,or severe motion sickness, making the user unable to tolerate VR devices; 5. History of acute diabetic complications within the past 3 months (diabetic ketoacidosis, hyperglycemic hyperosmolar state, severe hypoglycemia, etc.); 6. Severe impairment of vital organ function, including cardiac, hepatic, or renal dysfunction; 7. Pregnant or breastfeeding women, or women planning to become pregnant during the study; 8. Contraindications for MRI scans, such as the presence of metallic prostheses, pacemakers, cochlear implants, or other metallic implants, or claustrophobia; 9. Participation in other clinical trials currently or within the past 3 months; 10. Known or suspected history of allergy to study-related materials; 11. Currently taking medications intended to improve cognitive function.

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: China

  • Jiangsu, China: 1

Sample of listed locations

  • Department of Endocrinology, the Affiliated Drum Tower Hospital of Nanjing University Medical School — Nanjing, Jiangsu, 210008, China — Site recruitment status not specified in the registry data

Study details

Start date
June 1, 2026
Primary completion date
December 30, 2027
First posted
June 16, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07650318
Registry last updated
September 18, 2026
QualifiedStudies registry data refreshed
September 21, 2026

View NCT07650318 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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