We have an extensively diverse, ever-growing community network M-CEN (Marginalised Community Engagement Network), which is designed for reaching into the heart of marginalised communities, ensuring to bring there voices to the forefront and helping reduce health inequalities.

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Working with community of interest in health research is vital for several reasons. First, community groups provide valuable insights into the specific health needs and concerns of their populations, ensuring that research addresses relevant and pressing issues. Their involvement helps to design studies that are culturally sensitive and ethically sound, fostering trust and cooperation between researchers and participants.

 

Additionally, community engagement enhances the recruitment and retention of study participants. People are more likely to participate in research if they see their communities involved and benefiting from the outcomes. This participation leads to more robust data and more accurate findings, which are crucial for developing effective health interventions and policies.

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Community groups also play a critical role in disseminating research findings. They help translate complex scientific results into practical, understandable information that can be used to improve public health. By involving community groups in every stage of the research process, from planning to implementation to dissemination, researchers ensure that their work is relevant, respectful, and beneficial to those it aims to serve.

Overall, collaboration with community groups promotes a more inclusive, equitable, and impactful approach to health research, ultimately leading to better health outcomes and stronger, healthier communities.