cognitive impairment, frail
Conditions
Interventions
Intervention group:A 12-week, home-based exercise program with Vivifrail's individualized multi-component intervention and 7 weeks of metamemory intervention training
screening (Questionnaire survey, indicators include: ? socio-demographic data, such as age, gender, education, marital status, number of children, type of occupation, income, household registration, e
? other survey instruments: A. depression: Chinese version of the Geriatric Depression Scale (15-item GDS-15 and 30-item Geriatric Depression Scale, GDS-30)
B. function of daily living: assessment of activities of daily living (ADL)
C. Pittsburgh Sleep Quality Index (PSQI). (Geriatric Depression Scale, GDS-30)
B. Functioning of daily living: assessment of activities of daily living (ADL)
C. Pittsburgh sleep quality index (PSQI)
D. PSQI)
D. Physical Activity Scale for the Elderly (PASE)
E. MMSE ( Minimum Mental State Examination)
F. Mini- Nutritional Assessment (MNA)
G. The Short Physical Performance Battery-SPPB (SPPB).):None
Control group:Receive health education through information brochures on chronic diseases, hypertension, diabetes, etc.
Sponsors
Fudan University School of Public Health
Eligibility
Sex/Gender
All
Age
60 Years to 120 Years
Inclusion criteria
Inclusion criteria: (1) Cross-sectional survey: =60 years of age; (2) Randomized controlled trial: ?=60 years old, Barthel index score =60, able to communicate and walk; ?subjective report of memory or other cognitive decline; ?Simple Mental State Examination Scale (Mini-mental State Examination, MMSE) test score related to education level, inclusion criteria were: illiterate =19 points, elementary school = 22 points, junior high school and above = 26 points; ? a diagnosis of dementia had not been reached; ? pre-frailty or frailty assessed according to Fried criteria and the availability of relatives/caregivers to assist with motor monitoring.
Exclusion criteria
Exclusion criteria: Exclusion criteria: include, but are not limited to, the following: subject has any contraindication to physical exercise or testing; myocardial infarction in the past 3 months; angina pectoris; cancer; arrhythmia; unstable cardiovascular disease or other unstable medical condition; arterial hypertension; recent pulmonary thromboembolism; upper or lower extremity fracture within the past 3 months; and unwillingness to complete study requirements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| cognitive function;FRAIL; | — |
Countries
China
Contacts
Public ContactYing Wang
Fudan University School of Public Health
Outcome results
None listed