9. Outcomes: patient/carer quality of life.
Secondary outcomes: patient/family member/carer quality of life | |||
Study ID | Patient quality of life | Timing (longest follow‐up) | Scale, scoring |
Agar 2017 | X | 3‐monthly | Quality of life in Late‐stage Dementia (QUALID); 11‐item scale. Nurse‐rated No data |
Bernacki 2019 | X | Unclear | SF‐12 V2 health survey (QoL and general physical health function) No data |
Epstein 2017 | X | 3‐monthly to 3 years | Composite QoL score as average of 5 z‐scored subscales: McGillQoL scale single item, McGill Psychological Well‐Being subscale, McGill Existential Well‐Being subscale, FACT‐G Physical Functioning subscale, FACT‐G Social Functioning subscale Research‐administered questionnaire/interview |
Walczak 2017 | X | 1 month | Health‐related QoL (FACT‐G) |
X: outcome assessed.
QoL: quality of life.