persons with cognitive impairment
Conditions
Interventions
The intervention group received a high-quality activity program during hospitalization.
The non-intervention group received usual occupational therapy during hospitalization.
Sponsors
Osaka University of Human Sciences
multiple hospitals in Japan
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Diagnosis of an orthopedic condition or disuse syndrome 2. Presence of cognitive impairment 3. Admission to a convalescent rehabilitation hospital
Exclusion criteria
Exclusion criteria: 1. Individuals from whom informed consent to participate in the study could not be obtained from the participant or a legally authorized representative 2. Individuals judged to have difficulty participating in the study due to physical or mental conditions 3. Individuals for whom MMSE administration was not feasible and whose dementia severity could not be adequately assessed
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| behavioral and psychological symptoms, quality of life, and emotional function | — |
Secondary
| Measure | Time frame |
|---|---|
| cognitive function and caregiver burden | — |
Countries
Japan
Contacts
Public ContactYuki Nakagawa
Osaka University of Human Sciences, Japan Faculty of Health Sciences
Outcome results
None listed