General guidelines for payment, reimbursement and recognition of consumers across different levels of involvement and examples of what those activities may look like. These guidelines provide general advice taking into account the range of contextual factors that need to be considered for each project or activity. Please note, some funders or organisations may have their […]
Guidelines for remuneration and reimbursement of consumers across different levels of involvement in health and medical research with good practice examples.
CES4Health.info is a free, online platform for peer-reviewing, publishing and disseminating products of health-related community-engaged scholarship that are in forms other than journal articles. For example, videos, manuals, curricula and products developed through community-based participatory research and other community engaged work.
PCORI’s searchable database link to articles on best practices, lessons learned and other topics related to engagement in health research. The resources are useful for anyone looking to learn about engaging patients, communities and other partners in health research.
A practical guide to co-production and its application in research and health service settings, aiming to make public partnerships more diverse, inclusive, and impactful.
Free 30 minute self-paced online course on including consumer and community involvement in grant writing. Includes tips to enhance the chance of grant success by including integral CCI components in relevant aspects of grant applications. Participants will receive a certificate of completion at the end of the course.
Free 30 minute self-paced online course that describes the fundamentals of consumer and community involvement in health research. Designed for consumers, community members, researchers, administrators, policy makers and organisations involved in health research. Participants will receive a certificate of completion at the end of the course.
A clear, step-by-step guide for embedding meaningful consumer and community involvement into health and medical research systems. The Handbook is designed to be adaptable and user-friendly, encouraging organisations and individuals to tailor it to their specific context and needs. There are also dedicated resources for consumers on topics such as approaching an organisation and assessing […]
A series of six self-paced online modules, providing general and practical information and strategies to meaningfully conduct and embed consumer and community involvement in research and healthcare improvement projects.
The toolkit provides practical advice for researchers and research organisations wishing to conduct patient-centred clinical trials. Using an interactive map, the Toolkit provides guidance and tools to help plan, deliver, evaluate and report consumer and community involvement and engagement activities. The Toolkit also contains a small but growing collection of dedicated resources for consumers and […]
Practical strategies to seek and support diverse engagement and participation, as well as tips for success.
This framework lists a range of strategies that enable current or potential consumers to participate in service planning and decision making. Additional considerations for Culturally and Linguistically Diverse communities are included.