The research sought to explore the views of members of the public on the value to patients of the revised version of Good Medical Practice, the General Medical Council’s ethical guidance…
During the late part of 2007, as part of the development of the National Service Framework (NSF) Picker undertook research with Chronic Obstructive Pulmonary Disease (COPD) patients (and their carers)…
The purpose of the Patient-Centred Professionalism project was “to define patient-centred professionalism in medicine, and to help embed the essential principles in the culture of the medical profession so that…
National indicators and survey questions are available for many care settings and patient conditions. But ‘patient experience’ can cover a very wide range of aspects of the organisation and delivery…
Many patients expect to play an active role in managing their own health care. A growing body of evidence shows that people who are actively involved in protecting their health…
The first national survey of parents’ experiences of neonatal care was carried out in 2010-11 with 125 neonatal units, including special care baby units, local neonatal units and neonatal intensive…
A study was carried out to determine the current quality of health information and to assess the added value of accrediting information providers. The study consisted of four components: a)…
We worked with Lymphoma Coalition on the 2020 iteration of their biannual Global Patient Survey. The survey seeks to understand patient experience in lymphomas as well as the impact of…
The Adult Inpatient Survey asked recent hospital patients about their experiences from admission to discharge….
The first patient experience survey of people living with Sickle Cell Disease (SCD) revealed information provision and lack of public awareness are some of the biggest issues affecting patient experiences….