Search Results
22. Patient-reported outcome measures in oral lichen planus: A comprehensive review of the literature with focus on psychometric properties and interpretability
23. Utilization of a Wide Array of Nonvalidated Outcome Scales in Pediatric Orthopaedic Publications: Can't We All Measure the Same Thing?
24. A critical review of patient and parent caregiver oriented tools to assess health-related quality of life, activity of daily living and caregiver burden in spinal muscular atrophy
25. Evidence-Base Update for Parenting Stress Measures in Clinical Samples
26. Measures for social support in raising a child with a disability: A scoping review
27. Tools Measuring Quality of Death, Dying, and Care, Completed after Death: Systematic Review of Psychometric Properties
28. Coping Assessment Tools in the Family Caregivers of Patients with Breast Cancer: A Systematic Review
29. Living with Chronic Illness from the Family Perspective:An Integrative Review
30. Patient-reported Outcome Measures (PROMs) in Pediatric Non-Malignant Hematology: A Systematic Review
31. A psychometric appraisal of positive psychology outcome measures in use with carers of people living with dementia: a systematic review
32. Assessing unmet needs in advanced cancer patients: a systematic review of the development, content, and quality of available instruments
33. Family reported outcomes, an unmet need in the management of a patient's disease: appraisal of the literature
34. Measures used to assess impact of providing care among informal caregivers of persons with stroke, spinal cord injury, or amputation: a systematic review
35. Outcome Measures Following Critical Illness in Children With Disabilities: A Scoping Review
36. Assessment of patient-reported outcome measures used in corneal transplantation: a systematic review
37. Caregiver Burden and Dementia: A Systematic Review of Self-Report Instruments
38. Evaluation of Psychometric Properties of Hardiness Scales: A Systematic Review
39. Implementation of patient-reported outcome measures in a heart transplant recipient registry: First step toward a patient-centered approach
40. Measuring carer quality of life in Duchenne muscular dystrophy: a systematic review of the reliability and validity of self-report instruments using COSMIN
- « Previous
- Next »
- 1
- 2
- 3