Michele Peters

• Treatment outcomes in schizophrenia: qualitative study of the views of family carers.

  Lloyd J. et al, (2017), BMC Psychiatry, 17

• The role of life context and self-defined well-being in the outcomes that matter to people with a diagnosis of schizophrenia.

  Lloyd H. et al, (2017), Health Expect

• Derivation and Validation of a Modified Short Form of the Stroke Impact Scale.

  MacIsaac R. et al, (2016), J Am Heart Assoc, 5

• The Long-Term Conditions Questionnaire: conceptual framework and item development.

  Peters M. et al, (2016), Patient Relat Outcome Meas, 7, 109 - 125

• Refinement of the Long-Term Conditions Questionnaire (LTCQ): patient and expert stakeholder opinion.

  Kelly L. et al, (2016), Patient Relat Outcome Meas, 7, 183 - 193

• Psychometric properties of carer-reported outcome measures in palliative care: A systematic review.

  Michels CT. et al, (2016), Palliat Med, 30, 23 - 44

• Perspectives from health, social care and policy stakeholders on the value of a single self-report outcome measure across long-term conditions: a qualitative study.

  Hunter C. et al, (2015), BMJ Open, 5

• Cancer PROMs: a scoping study

  Coulter A. et al, (2015)

• Change in health status in long-term conditions over a one year period: a cohort survey using patient-reported outcome measures.

  Peters M. et al, (2014), Health Qual Life Outcomes, 12

• The routine collection of patient-reported outcome measures (PROMs) for long-term conditions in primary care: A cohort survey

  Peters M. et al, (2014), BMJ Open, 4

• The routine collection of patient-reported outcome measures (PROMs) for long-term conditions in primary care: a cohort survey.

  Peters M. et al, (2014), BMJ Open, 4

• Quality of life and burden in caregivers for patients with PD

  Peters M., (2014), Focus on Parkinson's Disease, 24, 44 - 48

• The Stroke Impact Scale: validation in a UK setting and development of a SIS short form and SIS index.

  Jenkinson C. et al, (2013), Stroke, 44, 2532 - 2535

• Carer quality of life and experiences of health services: a cross-sectional survey across three neurological conditions.

  Peters M. et al, (2013), Health Qual Life Outcomes, 11

• The PDQ-Carer: development and validation of a summary index score.

  Morley D. et al, (2013), Parkinsonism Relat Disord, 19, 448 - 449

• Patients’ experiences of health and social care in long-term neurological conditions in England: a cross-sectional survey

  Peters M. et al, (2013), Journal of Health Services Research & Policy, 18, 28 - 33

• Patients' experiences of health and social care in long-term neurological conditions in England: a cross-sectional survey.

  Peters M. et al, (2013), J Health Serv Res Policy, 18, 28 - 33

• Quality in the provision of headache care. 1: systematic review of the literature and commentary.

  Peters M. et al, (2012), J Headache Pain, 13, 437 - 447

• Quality in the provision of headache care. 2: defining quality and its indicators.

  Peters M. et al, (2012), J Headache Pain, 13, 449 - 457

• Quality in the provision of headache care. 2: Defining quality and its indicators

  Peters M. et al, (2012), Journal of Headache and Pain, 13, 449 - 457

• Quality in the provision of headache care. 1: Systematic review of the literature and commentary

  Peters M. et al, (2012), Journal of Headache and Pain, 13, 437 - 447

• The development and validation of a quality of life measure for the carers of people with Parkinson's disease (the PDQ-Carer)

  Jenkinson C. et al, (2012), Parkinsonism and Related Disorders, 18, 483 - 487

• The development and validation of a quality of life measure for the carers of people with Parkinson's disease (the PDQ-Carer).

  Jenkinson C. et al, (2012), Parkinsonism Relat Disord, 18, 483 - 487

• The impact of perceived lack of support provided by health and social care services to caregivers of people with motor neuron disease.

  Peters M. et al, (2012), Amyotroph Lateral Scler, 13, 223 - 228

• Factors influencing quality of life in caregivers of people with Parkinson's disease and implications for clinical guidelines.

  Morley D. et al, (2012), Parkinsons Dis, 2012

• DEVELOPING A MEASURE OF PARKINSON'S CARER QUALITY OF LIFE (PDQ-CARER)

  Jenkinson C. et al, (2011), EUROPEAN JOURNAL OF NEUROLOGY, 18, 644 - 644

• ‘‘Quality’’ in Headache Care. What Is It and How Can It Be Measured?

  Peters M. et al, (2011), Handbook of Headache

• Does self-reported well-being of patients with Parkinson's disease influence caregiver strain and quality of life?

  Peters M. et al, (2011), Parkinsonism Relat Disord, 17, 348 - 352

• Translating patient-reported outcome measures (PROMs) for cross-cultural studies

  Peters M., (2011), Quality of Life Measurement in Neurodegenerative and Related Conditions

• Quality of Life Measurement in Neurodegenerative and Related Conditions

  Jenkinson C. et al, (2011)

• Outcome measures for informal carers of individuals with neurodegenerative conditions

  Peters M., (2011), Quality of Life Measurement in Neurodegenerative and Related Conditions

• The relationship between well-being and support provided by health and social services to caregivers of people with motor neurone disease

  Peters M. et al

Recent Publications

• Treatment outcomes in schizophrenia: qualitative study of the views of family carers.

  Lloyd J. et al, (2017), BMC Psychiatry, 17

• The role of life context and self-defined well-being in the outcomes that matter to people with a diagnosis of schizophrenia.

  Lloyd H. et al, (2017), Health Expect

• Derivation and Validation of a Modified Short Form of the Stroke Impact Scale.

  MacIsaac R. et al, (2016), J Am Heart Assoc, 5

• The Long-Term Conditions Questionnaire: conceptual framework and item development.

  Peters M. et al, (2016), Patient Relat Outcome Meas, 7, 109 - 125

• Refinement of the Long-Term Conditions Questionnaire (LTCQ): patient and expert stakeholder opinion.

  Kelly L. et al, (2016), Patient Relat Outcome Meas, 7, 183 - 193