Skip to content

Construction and preliminary application of the community-based non-pharmacological intervention program for older adults with subjective cognitive decline

Construction and preliminary application of the community-based group non-pharmacological intervention program for older adults with subjective cognitive decline

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107700
Enrollment
Unknown
Registered
2025-08-18
Start date
2025-08-18
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

Subjective cognitive decline

Interventions

Experimental group:Multidisciplinary non-pharmacological interventions: cognitive intervention + exercise intervention + lifestyle intervention, etc.

Sponsors

China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Age>=60 years old; 2. Meet the SCD screening criteria: > score of the Chinese version of the Subjective Cognitive Decline Questionnaire (SCD-Q9). =5 points; No objective cognitive impairment, as determined by the Montreal Cognitive Assessment (MoCA) and Mini-Mental State Examination (MMSE); The ability to perform daily activities is not affected; 3. Have not engaged in regular exercise and cognitive activities in the past six months; 4. Informed consent and voluntary participation.

Exclusion criteria

Exclusion criteria: 1. Any other neurodegenerative or major mental illness (mild cognitive impairment or dementia, etc.); 2. Any serious or unstable medical illness (i.e., unstable or severe asthma or cardiovascular disease, active gastric ulcer, or severe liver or kidney disease or uncontrollable hypertension); 3. Severe anxiety and depression; 4. Those who have contraindications to exercise, color blindness, or too low education to cooperate with the test; 5. Those who are participating in other research trials.

Design outcomes

Primary

MeasureTime frame
Subjective memory;Gobal cognitive function;Episodic memory;Executive function;Attention;Physical activity level;Timed "Up and Go" test;

Secondary

MeasureTime frame
Depression;Anxiety;Social network;Social participation;Activities of Daily Living ;Feedback from the intervention subjects;

Countries

China

Contacts

Public ContactGuohua Tang

China Medical University

tgh204203@163.com+86 189 4022 6278

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026