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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