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Responsiveness Study
Responsiveness of primary care services: development of a patient-report measureTimescale: October 2010 – September 2013 Funder: Service Delivery & Organisation
Dr Carolyn Tarrant, Prof Richard Baker, Prof Peter Jackson (University of Leicester) Prof George Freeman (St George’s, London) Prof Mary Boulton (Oxford Brookes University) Dr Patricia Wilkie (National Association for Patient Participation)
Interviewer: Janet Willars (University of Leicester) Administrative support: Lisa Hallam (University of Leicester)
For further information about the study, please contact: Emma Angell, Researcher, 0116 229 7256, elj1@lea.c.uk Carolyn Tarrant, Principal Investigator, 0116 229 7234, ccp3@le.ac.uk
Summary of the studyProviders of primary care services do not always respond well to the needs of different groups of patients, and certain groups of patients are often underserved. Practices are increasingly being encouraged to become more responsive to the needs of their patients. Our aim in this study is to develop a questionnaire to measure responsiveness that can be used by diverse patient groups (including those with sensory disability, and those who do not read or write English). It will be designed so that it is suitable for use by a range of different primary care organisations (PCOs), including GP practices and walk-in centres.
This will involve, first of all, finding out what responsiveness means. We will do a literature review, and interviews and focus groups with up to 50 patients and 20 staff in 12 PCOs in Leicestershire, Northamptonshire and Rutland. We will develop a questionnaire and test it with 300 patients from six PCOs. We will then ask 15 PCOs across three different regions of the UK to send it to a total of 3,000 patients. By doing this we can find out if it is a good measure of responsiveness, and check it for consistency. We will ask staff how useful the results are to them.
Aims and objectivesOur aim in this study is to develop a patient report instrument to measure practice responsiveness. The measure will be reliable, valid, and appropriate for use across diverse patient groups, and will be designed for use by a range of different primary care service providers.
Our objectives are:
To view a lay summary of the project, please click here To view the full protocol, please click here
Progress to date:
Stage 1 of the project is drawing to a close. We have completed our interviews with patients and staff and analysed the transcripts. The themes that emerged from the interviews were used to develop eight questions about responsive primary care. These questions were taken to three diverse focus groups (people with disabilities, members of a patient participation group at a GP practice in a deprived area, non-English speakers) where participants were asked about what they considered when they answered the questions, any misunderstandings that arose, and suggestions for improvement. The analysis of the transcripts has produced some extremely useful feedback that will help us to amend the questions so they can be more easily understood. The next draft of our questions will be shared with the advisory group and will be refined in response to feedback. We will also be asking the advisory group to indicate which formats would be the most promising for us to pursue in the first instance. Stage 2 of the project will being in June when we begin the first pilot. [Updated on 22 March 2012]
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