The Voice of Patients – A Partner to Clinicians – A Catalyst for Change
For clinicians and researchers
Talk to us while your study or service is still being planned, when patient input can still make a difference.
Study design and choosing outcomes
Grant applications, as named collaborators
Recruitment, and why people say no
Patient information and consent forms
Trial steering and oversight committees
Guidelines and consultation responses
Service and pathway redesign
Shared decision making
Our members range from people recently diagnosed to people with years on trial committees and national boards. Many bring professional backgrounds too. Get in touch with a question you haven't answered yet, and we'll bring the right members together.
Get in touch