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A Study on the Application of Moderate-Intensity Aerobic Calisthenics in Rural Elderly with Motoric Cognitive Risk Syndrome

A Study on the Application of Moderate-Intensity Aerobic Calisthenics in Rural Elderly with Motoric Cognitive Risk Syndrome

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128058
Enrollment
Unknown
Registered
2026-07-13
Start date
2026-07-13
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Motoric Cognitive Risk Syndrome

Interventions

Intervention group:Based on routine health education, the intervention group receives a 12-week moderate-intensity aerobic exercise intervention (Jiamusi Happy Dance Steps) lasting 60 minutes per sess
control group:While maintaining the normal daily routine, provide relevant knowledge about the health education of cognitive risk syndrome for exercise and obtain the health education manual for cogni

Sponsors

Fujian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=60 years; 2. Meeting the diagnostic criteria for Motor Cognitive Risk Syndrome (MCR); 3. Clear consciousness and ability to communicate clearly; 4. Permanent residents of rural areas in nine prefecture-level cities of Fujian Province (with an annual residence of >=9 months) and no plan to relocate within the next year; 5. Willing to voluntarily participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Presence of severe mental disorders, history of stroke, Parkinson's disease, or severe visual/auditory impairments; 2. Physical disability that prevents independent walking; 3. Comorbid severe systemic diseases, such as cardiopulmonary conditions; 4. Regular exercise habits within the past 6 months (>=30 minutes/day, >=3 days/week) or a long-term history of exercise; 5. Current participation in other interventional studies.

Design outcomes

Primary

MeasureTime frame
Montreal Cognitive Assessment Basic;

Secondary

MeasureTime frame
Subjective Cognitive Decline-questionnaire 9;short physical performance battery , SPPB;body fat;12-Item Short-Form Health Survey, SF-12;Patient Health Questionnaire-9, PHQ-9;Generalized Anxiety Disorder-7 item, GAD-7;World Health Organization Well-being Index,WHO-5;The Theory of Planned Behavior Questionnaire (Exercise Version);

Countries

China

Contacts

Public ContactLi Hong

Fujian Medical University,

leehong99@126.com+86 137 0507 0219

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026