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Study on Community Identification and Intervention for Older Adults with Mild Cognitive Impairment

Research on Identification and Community Support for Mild Cognitive Impairment in Older Adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127765
Enrollment
Unknown
Registered
2026-07-07
Start date
2026-07-10
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Cognitive Impairment

Interventions

Intervention group:Receive multidimensional non-pharmacological interventions
Control group:None

Sponsors

Tianjin University of Technology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age >= 60 years; 2. Meet the diagnostic criteria for mild cognitive impairment (MCI) (MoCA score of 18–25 or equivalent); 3. Community-dwelling; 4. Essentially independent in daily living; 5. Willing to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Diagnosed with dementia (e.g., Alzheimer's disease, vascular dementia, etc.) or other neurodegenerative diseases causing cognitive impairment; 2. Presence of severe mental disorders (e.g., major depression, schizophrenia, bipolar disorder, etc.) or currently in an acute phase of psychiatric symptoms; 3. Severe visual, auditory, or speech impairments that prevent cooperation with cognitive assessment or intervention activities; 4. Complicated with severe physical illnesses (e.g., severe cardiac insufficiency, acute exacerbation of chronic obstructive pulmonary disease, active chemotherapy/radiotherapy for malignant tumors, etc.) that preclude completion of the intervention; 5. Currently participating in other similar cognitive intervention studies or taking medications known to affect cognitive function (e.g., antipsychotics, antiepileptics, etc.); 6. History of alcohol or drug dependence with ongoing active use or not yet in remission; 7. Other conditions that, in the investigator’s judgment, make the participant unsuitable for the study (e.g., inability to ensure follow-up compliance, etc.).

Design outcomes

Primary

MeasureTime frame
Montreal Cognitive Assessment (MoCA);Mini-Mental State Examination (MMSE);Activities of Daily Living Scale (ADL);

Secondary

MeasureTime frame
Geriatric Depression Scale (GDS);Quality of Life Scale (QoL);General Self-Efficacy Scale (GSES);Short Physical Performance Battery (SPPB); Pittsburgh Sleep Quality Index (PSQI);

Countries

China

Contacts

Public ContactSun Jinming

Tianjin University of Technology

sunjinming@email.tjut.edu.cn+86 183 3069 8678

Outcome results

None listed

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