INFANCY — International Neuromodulation for All Neuroatypical Children Society
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Collaborative evidence

Build evidence that is larger, longer, and more useful.

INFANCY supports collaboration around studies and registries designed to answer clinically meaningful questions while protecting participants, respecting families, and improving the quality and comparability of pediatric evidence.

01

Public study listings

Each listing should state the study title, purpose, population, modality, condition, locations, status, sponsor, principal investigators, registry identifier, contact, and whether recruitment is open.

02

For researchers

INFANCY can help investigators identify collaborators, refine shared outcomes, connect sites, discuss feasibility, and develop working groups around multicenter questions. INFANCY endorsement or sponsorship must follow a formal review process.

03

For families

Study listings are informational and do not replace discussion with a child’s clinical team. Participation decisions should follow independent informed-consent processes and approved research oversight.

Founding note

Active studies will be added only after verification with the responsible investigator and public registry record.

NEXT STEP

Propose a collaboration

Share a multicenter question, registry concept, methods need, or opportunity for shared infrastructure.

Propose an initiative