about
The Long-Term Conditions Questionnaire: conceptual framework and item developmentTreatment outcomes in schizophrenia: qualitative study of the views of family carersPerspectives from health, social care and policy stakeholders on the value of a single self-report outcome measure across long-term conditions: a qualitative study.Psychometric properties of carer-reported outcome measures in palliative care: A systematic reviewDerivation and Validation of a Modified Short Form of the Stroke Impact ScaleThe patients' perceptions of migraine and chronic daily headache: a qualitative study.Quality in the provision of headache care. 2: defining quality and its indicators.Factors influencing quality of life in caregivers of people with Parkinson's disease and implications for clinical guidelines.Migraine and chronic daily headache management: implications for primary care practitioners.Refinement of the Long-Term Conditions Questionnaire (LTCQ): patient and expert stakeholder opinion.The routine collection of patient-reported outcome measures (PROMs) for long-term conditions in primary care: a cohort survey.The role of life context and self-defined well-being in the outcomes that matter to people with a diagnosis of schizophrenia.The PDQ-Carer: development and validation of a summary index score.The development and validation of a quality of life measure for the carers of people with Parkinson's disease (the PDQ-Carer).Patients' experiences of health and social care in long-term neurological conditions in England: a cross-sectional survey.Long-Term Conditions Questionnaire (LTCQ): initial validation survey among primary care patients and social care recipients in England.Translating instruments for cross-cultural studies in headache research.The context of coping: a qualitative exploration of underlying inequalities that influence health services support for people living with long-term conditions.Does self-reported well-being of patients with Parkinson's disease influence caregiver strain and quality of life?Quality of life and burden of morbidity in primary care users with multimorbidity.Quality of life in coeliac disease: item reduction, scale development and psychometric evaluation of the Coeliac Disease Assessment Questionnaire (CDAQ)Self-efficacy and health-related quality of life: a cross-sectional study of primary care patients with multi-morbidityInformal carers' experience of assistive technology use in dementia care at home: a systematic review.Research into headache: the contribution of qualitative methodsPatients' decision-making for migraine and chronic daily headache management. A qualitative studyPatients' management of migraine and chronic daily headache: a study of the members of the Migraine Action Association (United Kingdom)Reducing demand for antibiotic prescriptions: evidence from an online survey of the general public on the interaction between preferences, beliefs and information, United Kingdom, 2015Enhancing primary care support for informal carers: A scoping study with professional stakeholdersAids to management of headache disorders in primary care (2nd edition) : on behalf of the European Headache Federation and Lifting The Burden: the Global Campaign against HeadacheWithdrawing gluten-free food from prescriptions in England: a mixed-methods study to examine the impact of policy changes on quality of lifeHealthcare experiences and quality of life of adults with coeliac disease: a cross-sectional study
P50
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P50
description
onderzoeker
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հետազոտող
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Michele Peters
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Michele Peters
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Michele Peters
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Michele Peters
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Michele Peters
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Michele Peters
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Michele Peters
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P106
P31
P496
0000-0002-0076-5981