Effect of the Group-based Paro Intervention on Physiological and Psychological Outcomes
Dementia, Mild, Dementia Moderate, Cognitive Impairment
About this trial
This is an interventional health services research trial for Dementia, Mild focused on measuring Dementia, Paro, Neurobiology, Cognitive Function, Mental well-being
Eligibility Criteria
Inclusion Criteria:
(1) aged 65 years or over; (2) Mild to moderator dementia (3) an ability to communicate in Mandarin or Taiwanese; and (4) has been living in the LTC facility at least 3 months
Exclusion Criteria:
(1) have severe difficulty in communication; (2) are totally dependent on carers for daily activity; (3) have a diagnosed infectious disease, severe dementia, and severe mental illness such as schizophrenia and delusional disorder
Sites / Locations
- National Cheng Kung University Hospital Dou-Liou Branch
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Paro intervention group
control group
Participants in the Paro intervention group will receive a group (6-8 people as a group), facilitated, and 30-minute weekly session Paro intervention for 6 weeks.
The control group will receive care as usual activities, such as painting, drawing, and craft, which are provided by each facility.