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2. Use of family proxies in quality of life research for cancer patients at the end of life: a literature review
3. Care for the caregivers: a review of self-report instruments developed to measure the burden, needs, and quality of life of informal caregivers
4. Measures used to assess burden among caregivers of stroke patients: a review
5. A review of instruments developed to measure outcomes for carers of people with mental health problems
6. Parental functioning in the context of adolescent chronic pain: a review of previously used measures
7. Condition-specific quality of life questionnaires for caregivers of children with pediatric conditions: a systematic review
8. The measurement of burden of care in serious mental illness: a qualitative review
9. Patient Reported Outcomes Instruments in Schizophrenia: A Review of Psychometric Properties
10. Assessing the needs of informal caregivers to cancer survivors: a review of the instruments
11. Systematic review of tools to measure outcomes for young children with autism spectrum disorder
12. Upper limb function in everyday life of children with cerebral palsy: description and review of parent report measures
13. Measuring the impact of informal elderly caregiving: a systematic review of tools
14. Psychometric properties of carer-reported outcome measures in palliative care: A systematic review
15. A systematic review of instruments assessing dimensions of distress among caregivers of adult and pediatric cancer patients
16. Core outcome measures for interventions to prevent or slow the progress of dementia for people living with mild to moderate dementia: Systematic review and consensus recommendations
17. Informal caregiving in COPD: A systematic review of instruments and their measurement properties
18. Measuring the impact of dermatological conditions on family and caregivers: a review of dermatology-specific instruments
19. Patient- and Caregiver-Reported Assessment Tools for Palliative Care: Summary of the 2017 Agency for Healthcare Research and Quality Technical Brief
20. Positive psychology outcome measures for family caregivers of people living with dementia: a systematic review
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