Research Themes


Understanding how information about care-related needs and quality of life can be used to optimally achieve person-centred goals for commissioning, regulation etc.


Developing methods to improve participation of ‘hard-to-engage’ and ‘seldom heard’ people in research and so enable their experiences to be reflected in the evidence base.


Finding ways to identify and best measure the needs, quality of life, well-being and health of people in way that is relevant to how they experience services and support.

Service Delivery

Developing the evidence-base about which specific interventions succeed in delivering person-centred outcomes.