Study identification and participant-data access
Track studies and data availability
Study eligibility and data availability are separate. Keep requests and reasons in the register; use secure research infrastructure for participant datasets. This canvas documents the process and is not the participant-data repository.
Flow diagram
Steps
Identify eligible studies
Use reproducible searches and retain multiple reports linked to each study.
Request data and permissions
Record contact, agreements, transfer scope and governance without identifiers.
Track availability and refusals
Distinguish eligible studies, data supplied and aggregate-only evidence.
Verify received data coverage
Reconcile expected arms, participants, outcomes and follow-up with study records.
Define synthesis availability groups
Record included IPD, unresolved datasets and unavailable data reasons.
Study identification and participant-data access
End flow
Tables and supporting information
Study access register
This register stores access metadata, not participant-level records.
Assumptions and rationale
Unavailable participant data can bias the evidence base; obtaining IPD is not an eligibility criterion unless justified prospectively.
Method and protocol evidence
Attach the protocol, methodological sources and versioned software specification supporting these decisions. Record citations and provenance; do not enter participant identifiers.