Caregiver Burden
Cross-source consensus on Caregiver Burden from 1 sources and 5 claims.
1 sources · 5 claims
Uses
Other
Other
Other
Highlighted claims
- Caregiver burden is measured at 3 and 12 months using the Zarit Caregiver Burden Interview-22. — Assessment of health-related quality of life, cognitive, physical and psychological impairments in critically ill adults after status epilepticus (POSEIDON 2): protocol for a multicentre longitudinal study
- POSEIDON 2 includes caregiver burden as a parallel outcome. — Assessment of health-related quality of life, cognitive, physical and psychological impairments in critically ill adults after status epilepticus (POSEIDON 2): protocol for a multicentre longitudinal study
- Higher ZBI-22 scores indicate greater caregiver burden. — Assessment of health-related quality of life, cognitive, physical and psychological impairments in critically ill adults after status epilepticus (POSEIDON 2): protocol for a multicentre longitudinal study
- A caregiver is the primary informal caregiver identified by the patient and usually provides unpaid practical or emotional support. — Assessment of health-related quality of life, cognitive, physical and psychological impairments in critically ill adults after status epilepticus (POSEIDON 2): protocol for a multicentre longitudinal study
- Caregivers provide separate written informed consent to participate. — Assessment of health-related quality of life, cognitive, physical and psychological impairments in critically ill adults after status epilepticus (POSEIDON 2): protocol for a multicentre longitudinal study