37 results on '"Jenkinson, Crispin"'
Search Results
2. Carers’ experiences of assistive technology use in dementia care: a cross sectional survey
3. Development of a patient-reported outcome measure (PROM) and change measure for use in early recovery following hip or knee replacement
4. Informal carers’ experience and outcomes of assistive technology use in dementia care in the community: a systematic review protocol
5. Informal carers’ experience of assistive technology use in dementia care at home: a systematic review
6. Correction to: multiple imputation for patient reported outcome measures in randomised controlled trials: advantages and disadvantages of imputing at the item, subscale or composite score level
7. Multiple imputation for patient reported outcome measures in randomised controlled trials: advantages and disadvantages of imputing at the item, subscale or composite score level
8. Association between spousal emotional abuse and reproductive outcomes of women in India: findings from cross-sectional analysis of the 2005–2006 National Family Health Survey
9. Predictors of activity and participation across neurodegenerative conditions: a comparison of people with motor neurone disease, multiple sclerosis and Parkinson’s disease
10. Psychometric validation of a multi-dimensional capability instrument for outcome measurement in mental health research (OxCAP-MH)
11. Spanish version of the Parkinson’s Disease Questionnaire–Carer (PDQ-Carer)
12. Proceedings of Patient Reported Outcome Measure’s (PROMs) Conference Sheffield 2016: advances in patient reported outcomes research
13. The current practice of handling and reporting missing outcome data in eight widely used PROMs in RCT publications: a review of the current literature
14. The current practice of handling and reporting missing outcome data in eight widely-used PROMS in RCT publications: are we doing well?
15. Meaningful health outcomes for paediatric neurodisability: Stakeholder prioritisation and appropriateness of patient reported outcome measures
16. Towards a shared vision for measureable and meaningful health outcomes for children and young people with neurodisability: qualitative research, Delphi survey, systematic review, and stakeholder prioritisation
17. Evaluating the psychometric properties of an e-based version of the 39-item Parkinson’s Disease Questionnaire
18. Change in health status in long-term conditions over a one year period: a cohort survey using patient-reported outcome measures
19. People with limiting long-term conditions report poorer experiences and more problems with hospital care
20. Patient reports of the outcomes of treatment: a structured review of approaches
21. Does stimulus predict the best candidates for deep brain stimulation for PD?
22. Can pain and function be distinguished in the Oxford Knee Score in a meaningful way? An exploratory and confirmatory factor analysis
23. Randomised controlled trial (RCT) of continuous positive airways pressure therapy (CPAP) versus placebo in the treatment of sleep apnoea
24. An exploration of social and economic outcome and associated health-related quality of life after critical illness in general intensive care unit survivors: a 12-month follow-up study
25. Carer quality of life and experiences of health services: a cross-sectional survey across three neurological conditions
26. Quality in the provision of headache care. 1: systematic review of the literature and commentary
27. Quality in the provision of headache care. 2: defining quality and its indicators
28. Do South Asian women with PCOS have poorer health-related quality of life than Caucasian women with PCOS? A comparative cross-sectional study
29. Evaluation of the American version of the 30-item Endometriosis Health Profile (EHP-30)
30. The use of the SF-36 questionnaire in adult survivors of childhood cancer: evaluation of data quality, score reliability, and scaling assumptions
31. A patient-based questionnaire to assess outcomes of foot surgery: Validation in the context of surgery for hallux valgus
32. Health-Related Quality of Life in Amyotrophic Lateral Sclerosis: Determining a Meaningful Deterioration
33. Evaluating the responsiveness of the endometriosis health profile questionnaire: The EHP-30
34. Development of the Short Form Endometriosis Health Profile Questionnaire: The EHP-5
35. Impact sur la qualit?? de vie et co??ts engendr??s par la maladie de Parkinson
36. Development and validation of a short measure of health status for individuals with amyotrophic lateral sclerosis/ motor neurone disease: the ALSAQ-40
37. Health-Related Quality-of-Life Measurement in Patients with Parkinson??s Disease
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