Research Framework
The shared architecture for RBD studies.
A reference structure covering study design, outcomes and reporting, so findings can be compared across sites and disciplines.
DiscoverInternational research initiative · placeholder
RBD-IBI connects researchers, clinicians, patients and partners across continents to advance the science of RBD — and turn shared evidence into shared progress.
RBD-IBI brings together research groups, health systems and patient communities under one shared framework, so that discoveries in one country can benefit people everywhere.
Our work spans the full research journey — from common protocols and shared datasets to clinical translation and public understanding — with equity and openness at every step.
Read more about our missionOne interoperable approach for how RBD research is designed, run and reported across our partner network. placeholder
The shared architecture for RBD studies.
A reference structure covering study design, outcomes and reporting, so findings can be compared across sites and disciplines.
DiscoverConnected sites, pooled samples.
Partner clinics and biorepositories linked by common protocols, enabling larger and more diverse studies than any single site alone.
DiscoverCurated data, reproducible results.
Open, documented datasets and living evidence reviews, governed under clear access and ethics conditions.
DiscoverGrowing the next generation.
Fellowship and exchange programmes that build research capacity in less-resourced settings, on an equal footing.
DiscoverValues below are labelled placeholders. They will be replaced with confirmed figures by the RBD-IBI team — never invented.
Four frontiers where the initiative is pushing methods and access. placeholder
Systematic reviews that update as the science moves, so guidance stays current.
Remote, low-cost measures that broaden who can meaningfully take part.
Recruitment explicitly designed around communities that are usually under-represented.
Shared, anonymised datasets with governed, fair access conditions.
If you or someone you love is affected by RBD, you may have questions and no easy answers yet. Our promise is simple: clear, trustworthy information in plain language, and routes to the help that exists.
placeholder Content for patients and carers is being written with patient partners and will cover:
Curated reviews, guidelines and publications from across the initiative. placeholder
Browse publicationsAnonymised, documented data with clear access conditions, ready for secondary research. placeholder
Access the dataProtocols and processes that help partner sites run studies to the shared standard. placeholder
See the guidesA durable funding and governance model keeps the initiative useful long after individual programmes end — protecting data, relationships and trust.
Read moreA growing coalition of universities, health systems and philanthropy. placeholder
Whether you lead research, deliver care or live with RBD — there is a way in. Start with the bridge.