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Development and Application of a Digital Sport Stacking Training System for Older Adults with Cognitive Impairment

Development and Application of a Digital Sport Stacking Training System for Older Adults with Cognitive Impairment

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126178
Enrollment
Unknown
Registered
2026-06-04
Start date
2026-07-10
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Alzheimers disease, mild cognitive impairment

Interventions

Trial group:Using a digital cup-stacking training system developed based on augmented reality (AR) technology for intervention
training frequency of 3 times per week, 1 hour each session
intervention period of 12 weeks.

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 60 years old; 2. MCI patients: Diagnosed as MCI according to the MCI diagnostic criteria published in the 'Chinese Guidelines for the Diagnosis and Treatment of Dementia and Cognitive Impairment' (2018 edition); 3. AD patients: (1) Diagnosed as AD according to the DSM-IV and the NINCDS-ADRDA diagnostic criteria; (2) MMSE score of 19-24 points; (3) CDR score of 0.5 or 1 point; 4. If taking anti-dementia drugs or mood stabilizers, a stable dose must be maintained for at least 3 months; 5. Clear consciousness, basic communication ability, and no impairment in vision or hearing; 6. Signed informed consent and voluntary participation in this study; 7. Living with family members or caregivers.

Exclusion criteria

Exclusion criteria: 1. Severe mental illness or use of antidepressant medications; 2. History of alcohol or drug abuse; 3. Engaging in regular exercise twice or more per week; 4. Any physical condition that would impede participation in the study plan (e.g., severe cardiovascular, musculoskeletal, or neurological diseases).

Design outcomes

Primary

MeasureTime frame
Overall cognitive function;

Secondary

MeasureTime frame
Visual-spatial ability;Attention;Activities of daily living;Electroencephalogram signal;Processing speed and execution functions;Vital signs(Heart rate, pulse, blood pressure, respiratory rate);Electromyography signal;Memory function;Psychological and behavioral symptoms;

Countries

China

Contacts

Public ContactDing Fu

The First Affiliated Hospital of Chongqing Medical University

734403117@qq.com+86 23 8901 1876

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026