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Development and evaluation of a creative expressive program for elderly patients with mild to moderate dementia

Development and evaluation of a creative expressive program for elderly patients with mild to moderate dementia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064838
Enrollment
Unknown
Registered
2022-10-19
Start date
2022-10-19
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Dementia

Interventions

Experimental group:creative expressive cognitive intervention
Control group:general social activities

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 101 Years

Inclusion criteria

Inclusion criteria: 1. Dementia patients: (1) Aged >=65 years, and meet the diagnostic criteria of WHO International Classification of Diseases ICD-10 dementia; (2) Patients with mild to moderate dementia with a CDR score of 1 or 2 with the assistance of the clinician; (3) The medication was stable and the condition was stable within 1 month; (4) Have a certain level of hearing and vision and retain certain hand function, can participate in the activity; (5) Patients or family members sign written informed consent. 2. Caregivers: (1) As a main caregivers to take care of patients with 30 days or more, and is expected to begin research can continue to care for patients after 4 months or more; (2) Have normal ability to read, understand and express Chinese, and cooperate with the participants; (3) Voluntarily participate in this study and cooperate with investigators.

Exclusion criteria

Exclusion criteria: 1. Dementia patients: (1) Patients with other mental disorders; (2) Dementia caused by brain tumors, multiple sclerosis, encephalitis, epilepsy, Parkinson's disease dementia and other diseases of the central nervous system; (3) Dementia caused by abnormal thyroid function, folic acid or vitamin B12 deficiency, persistent hypoglycemia and other metabolic and nutritional deficiencies; (4) Alcoholism, drug abuse and other diseases known to cause dementia; (5) Serious physical disease or other reasons can not tolerate or cooperate with the research. 2. Caregivers: Have serious physical diseases (such as heart failure, severe liver and kidney diseases, cancer, etc.) or mental diseases.

Design outcomes

Primary

MeasureTime frame
The Neuropsychiatric Inventory, NPI;Apathy Evaluation Scale-Informant, AES-I;

Secondary

MeasureTime frame
Mini-Mental State Examination, MMSE;The Subscales of the Functional Assessment of Communication Skills, SFACS;Quality of Life-Alzheimer's Disease, QOL-AD;Activity of Daily Living, ADL;Caregiver Burden Inventory, CBI;

Countries

China

Contacts

Public ContactLi Hong

Fujian Provincial Hospital

leehong99@126.com+86 13705070219

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026