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dc.contributor.authorFawkes, Carol
dc.date.accessioned2017-12-11T14:45:41Z
dc.date.available2017-12-11T14:45:41Z
dc.date.issued2017-10-13
dc.date.submitted2017-12-11T13:17:24.327Z
dc.identifier.citationFawkes, C. 2017. 1 The development, evaluation, and initial implementation of a national programme for the use and collation of patient reported outcome measures (PROMs) in osteopathic back pain services in the UK. Queen Mary University of London.en_US
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/29606
dc.descriptionPhDen_US
dc.description.abstractIntroduction The use of Patient Reported Outcome Measures (PROMs) to measure the effects of care is being advocated increasingly in clinical settings. Current patient data capture involves completion of paper questionnaires which is costly and environmentally perplexing. New innovations are required to balance the challenges of introducing data capture directly from patients while considering budgets, access to Information Technology, and the capability to use technological devices. Methods Two qualitative studies were undertaken to identify the views of patients and clinicians concerning electronic PROM data capture in osteopathic practice. One qualitative study involved patient interviews to identify their views on a selection of specific PROMs. Clinician focus groups and interviews (osteopaths, chiropractors, and physiotherapists) were undertaken concerning their views and experiences of using PROMs. Scoping of PROMs in musculoskeletal practice was undertaken followed by a systematic review of one identified PROM. The review and qualitative work informed the development of content for a mobile and web app for capturing PROM data. The app was piloted to evaluate feasibility, and the clinimetric performance of the included PROMs. Feedback from the pilot informed revisions to the app prior to implementation into osteopathic practice. Results Clinicians (n=46) identified a range of barriers and facilitators to PROM use. Patients (n=22) while generally more enthusiastic than clinicians welcomed the opportunity to provide feedback and although undaunted by the use of technology highlighted the need for assurances concerning confidentiality of data, and limits on data sharing. The systematic review identified good measurement properties for the Bournemouth (BQ). Piloting of the app involved 257 participants contributing 404 data returns: it performed well requiring minimal revision prior to implementation. Conclusions The app performed well demonstrating great potential for further development to collect outcome data in a musculoskeletal clinical setting.en_US
dc.description.sponsorshipNational Council for Osteopathic Research Institute of Osteopathyen_US
dc.language.isoenen_US
dc.publisherQueen Mary University of Londonen_US
dc.rightsThe copyright of this thesis rests with the author and no quotation from it or information derived from it may be published without the prior written consent of the author
dc.subjectPrimary Care and Public Healthen_US
dc.subjectpatient reported outcome measuresen_US
dc.subjectosteopathic back painen_US
dc.titleThe development, evaluation, and initial implementation of a national programme for the use and collation of patient reported outcome measures (PROMs) in osteopathic back pain services in the UK.en_US
dc.typeThesisen_US


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