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Publications

Use of the Oxford Participation and Activities Questionnaire in chronic obstructive pulmonary disease

MORLEY D. and JENKINSON C., (2019), Chronic Respiratory Disease

Informal carers' experience and outcomes of assistive technology use in dementia care in the community: a systematic review protocol.

Sriram V. et al, (2019), Syst Rev, 8

Pretesting newly generated items to complement the 39-item Parkinson’s Disease Questionnaire

MORLEY D. et al, (2019), Quality of Life Research

Informal carers' experience of assistive technology use in dementia care at home: a systematic review.

Sriram V. et al, (2019), BMC Geriatr, 19

Early recovery following lower limb arthroplasty: Qualitative interviews with patients undergoing elective hip and knee replacement surgery. Initial phase in the development of a patient-reported outcome measure.

Strickland LH. et al, (2018), J Clin Nurs, 27, 2598 - 2608

An Evaluation of a Near Real-Time Survey for Improving Patients’ Experiences of the Relational Aspects of Care.

Jenkinson C. and Kelly L., (2018), Health Services and Delivery Research

Living with breathlessness in chronic heart failure: a qualitative study.

Walthall H. et al, (2017), J Clin Nurs, 26, 2036 - 2044

Children’s and young people’s response to parental illness: introduction and overview

Morley DP. and Jenkinson C., (2017), Children and Young People’s Response to Parental Illness: A Handbook of Assessment and Practice, 1 - 4

Children and Young People’s Response to Parental Illness A Handbook of Assessment and Practice

Morley DP. et al, (2017)

Measuring the impact of parental illness

Kelly L. et al, (2017), Children’s and young people’s response to parental illness, 221 - 244

Patient-Reported Outcome Measure for Early Postoperative Recovery Following Lower Limb Arthroplasty: A Systematic Review.

Strickland LH. et al, (2016), J Arthroplasty, 31, 2933 - 2940

Examining the role of patients' experiences as a resource for choice and decision-making in health care: a creative, inter-disciplinary mixed method study in digital health

Ziebland S. et al, (2016), NIHR Journals library PGfAR

Spanish version of the Parkinson's Disease Questionnaire-Carer (PDQ-Carer).

Ferrer-Cascales R. et al, (2016), Health Qual Life Outcomes, 14

Pretesting an e-based version of the Oxford Participation and Activities Questionnaire (Ox-PAQ)

Kelly L. et al, (2016), Value in Health, 19, A485 - A485

THE COELIAC DISEASE ASSESSMENT QUESTIONNAIRE (CDAQ): DEVELOPMENT OF A PATIENT-REPORTED OUTCOME MEASURE

Crocker H. et al, (2016), VALUE IN HEALTH, 19, A595 - A595

Use of the Routine Activities Domain of the Oxford Participation & Activities Questionnaire (Ox-PAQ)

Kelly L. et al, (2016), Quality of Life Research, 25, 106 - 106

Psychometric properties of the coeliac disease assessment questionnaire (CDAQ)

Crocker H. et al, (2016), QUALITY OF LIFE RESEARCH, 25, 180 - 180

The coeliac disease assessment questionnaire (CDAQ): comparison of the paper and electronic versions

Peters M. et al, (2016), QUALITY OF LIFE RESEARCH, 25, 180 - 181

Validation of the long-term conditions questionnaire (LTCQ)

Potter C. et al, (2016), QUALITY OF LIFE RESEARCH, 25, 108 - 108

Cost-utility analysis of deep brain stimulation surgery plus best medical therapy versus best medical therapy in patients with Parkinson's: Economic evaluation alongside the PD SURG trial.

McIntosh E. et al, (2016), Mov Disord, 31, 1173 - 1182

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