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Publications

The affordability and obtainability of gluten-free foods for adults with coeliac disease following their withdrawal on prescription in England: A qualitative study.

Crocker H. et al, (2023), J Hum Nutr Diet

A core outcome set for randomised controlled trials of physical activity interventions: development and challenges.

Crocker H. et al, (2022), BMC public health, 22

Withdrawing gluten-free food from prescriptions in England: a mixed-methods study to examine the impact of policy changes on quality of life.

Peters M. et al, (2020), J Hum Nutr Diet, 33, 453 - 464

Measuring the benefits of the integration of health and social care: qualitative interviews with professional stakeholders and patient representatives.

Crocker H. et al, (2020), BMC Health Serv Res, 20

Healthcare experiences and quality of life of adults with coeliac disease: a cross-sectional study.

Crocker H. et al, (2020), J Hum Nutr Diet

Measures for the integration of health and social care services for long-term health conditions: a systematic review of reviews.

Kelly L. et al, (2020), BMC Health Serv Res, 20

Quality of life in coeliac disease: item reduction, scale development and psychometric evaluation of the Coeliac Disease Assessment Questionnaire (CDAQ).

Crocker H. et al, (2018), Aliment Pharmacol Ther, 48, 852 - 862

Quality of life in coeliac disease: qualitative interviews to develop candidate items for the Coeliac Disease Assessment Questionnaire.

Crocker H. et al, (2018), Patient Relat Outcome Meas, 9, 211 - 220

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

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

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

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

The Imitation Game as a Method for Exploring Knowledge(s) of Chronic Illness

Evans R. and Crocker? H., (2013), Methodological Innovations Online, 8, 34 - 52

Include forthcoming?