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A randomized controlled trial of computerized cognitive training combined with semaglutide in patients with diabetes mellitus complicated by mild cognitive impairment.

A randomized controlled trial of computerized cognitive training combined with semaglutide in patients with diabetes mellitus complicated by mild cognitive impairment.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126606
Enrollment
Unknown
Registered
2026-06-12
Start date
2023-03-07
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Diabetes was associated with mild cognitive impairment

Interventions

Cognitive training intervention group:On the basis of standardized diabetes treatment, participants received computerized multi-domain and adaptive cognitive training for 12 weeks, 30 minutes per day
Control group:Standardized diabetes treatment was provided
Semaglutide intervention group :Simeglutide was added to the diabetes treatment regimen, with subcutaneous injections once a week starting at 0.25mg and increasing the dose as needed after 4 weeks, up

Sponsors

Beijing Anzhen Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age 50-75 years; 2. At least 6 years of education, with corrected hearing and vision within normal limits; 3. Previous confirmed diagnosis of type 2 diabetes; 4. HbA1c between 6.0% and 8.5%; 5. Subjective complaint of cognitive decline within the past year; 6. Performance in any cognitive domain assessed by the Basic Cognitive Aptitude Tests (BCAT) is more than 1 standard deviation below the mean of the normal population; 7. Willingness to undergo cognitive function testing and randomization for the study, and ability to comply with follow-up requirements.

Exclusion criteria

Exclusion criteria: 1. Alcohol abuse or current use of medications that affect cognitive function (antihistamines, antipsychotics); 2. Cognitive impairment caused by neurological disorders such as traumatic brain injury, brain tumors, severe cerebrovascular disease, or Parkinson's disease; 3. Psychiatric disorders affecting cognitive function, such as severe depression, mania, bipolar disorder, or schizophrenia; 4. History of stroke within the past 6 months; prior neurosurgery; 5. Previously confirmed diagnosis of dementia; 6. Inability to master the use of cognitive training equipment after two training sessions totaling 120 minutes; 7. Use of GLP-RA within the past 3 months; medullary thyroid carcinoma; severe gastrointestinal diseases.

Design outcomes

Primary

MeasureTime frame
Changes in MoCA scores in each group;Changes in any cognitive domain, such as processing speed and working memory,;Prolonged delay in pCASL measurement has been associated with changes in blood flow perfusion in known cognitively relevant regions;

Secondary

MeasureTime frame
Change in MMSE;Diabetes pain scale score;WHO-5 happiness index;Emotion scale scores;Pittsburgh Sleep Scale scores;Daily living ability (scale) score;Prolonged delay pCASL measurement of perfusion changes in other brain regions;

Countries

China

Contacts

Public ContactTao Hong

Beijing Anzhen Hospital, Capital Medical University

vivientao@126.com+86 189 1077 8680

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026