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Construction and Application of a Reminiscence Intervention Program Incorporating Multisensory Stimulation for Community-Dwelling Older Adults with Mild Cognitive Impairment

Construction and Application of a Reminiscence Intervention Program Incorporating Multisensory Stimulation for Community-Dwelling Older Adults with Mild Cognitive Impairment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100250
Enrollment
Unknown
Registered
2025-04-07
Start date
2025-04-29
Completion date
Unknown
Last updated
2025-12-01

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

Conditions

Cognitive impairment

Interventions

Reminiscence Intervention Group for Multi-Sensory Stimulation Groups:The study requires participants to engage in a weekly multisensory group reminiscence intervention, with each group consisting of a
Blank control group:No intervention, control group routinely lives in community activities

Sponsors

Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Community-dwelling elderly with MCI aged >=65 years; 2. Meet the diagnostic criteria for MCI in the 2018 Chinese Dementia and Cognitive Impairment Guidelines; 3. MoCA score between 15 and 25, and impairment of one or more cognitive domains in cognitive tests; 4. No obvious hearing or visual impairment, with language communication ability, able to understand and perform simple operation tasks; 5. Voluntarily participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Exclude those who are unable to participate in group activities due to their own reasons, such as severe mental illness or lack of physical activity ability; 2. The elderly with severe cognitive impairment, diagnosed with dementia or diagnosed with other brain diseases affecting cognitive function, such as cerebral infarction, brain tumor, cerebral vascular disease, etc., were excluded. 3. Patients with severe hearing or vision impairment could not receive the intervention effectively; 4. Participated in similar reminiscence therapy or cognitive intervention programs within the past 3 months.

Design outcomes

Primary

MeasureTime frame
Cognitive function;

Secondary

MeasureTime frame
Daily living skills;Depression;Happiness;Loneliness;

Countries

China

Contacts

Public ContactLu Lin

Soochow University

linlu@suda.edu.cn+86 139 1311 5626

Outcome results

None listed

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