Reporting guidelines lookup — which checklist does my study need?
Journals increasingly require a completed reporting checklist at submission. This is the map: every major guideline, the study design it covers, and where to get the official checklist.
| Guideline | Use for | Core content | Checklist |
|---|---|---|---|
| CONSORT 2010 | Randomized controlled trials | 25-item checklist + participant flow diagram (enrollment → allocation → follow-up → analysis) | Checklist ↗ |
| SPIRIT 2013 | Trial protocols | 33 items for the protocol itself — required by many registries and funders | Checklist ↗ |
| STROBE | Observational studies (cohort, case-control, cross-sectional) | 22 items; separate flavors per design; STROBE-nut, RECORD and other extensions exist | Checklist ↗ |
| STARD 2015 | Diagnostic accuracy studies | 30 items + flow of participants through the index test and reference standard | Checklist ↗ |
| TRIPOD 2015 (+AI 2024) | Prediction model development/validation | Model specification, performance, validation; TRIPOD+AI covers machine-learning models | Checklist ↗ |
| CHEERS 2022 | Health economic evaluations | 28 items covering perspective, discounting, sensitivity analyses | Checklist ↗ |
| ARRIVE 2.0 | Animal (in vivo) research | "Essential 10" + recommended set for design, sample size, blinding | Checklist ↗ |
| Guideline | Use for | Core content | Checklist |
|---|---|---|---|
| PRISMA 2020 | Systematic reviews & meta-analyses | 27 items + the flow diagram of records identified → screened → included | Checklist ↗ |
| PRISMA-ScR | Scoping reviews | 20-item adaptation of PRISMA for scoping questions | Checklist ↗ |
| MOOSE | Meta-analyses of observational studies | Search, heterogeneity, and bias reporting specific to observational syntheses | Checklist ↗ |
| COREQ | Qualitative interviews & focus groups | 32 items: research team, methods, analysis and reporting | Checklist ↗ |
| SRQR | Qualitative research (any method) | 21 items; broader and less interview-specific than COREQ | Checklist ↗ |
| ENTREQ | Qualitative evidence syntheses | 21 items for meta-ethnography, thematic synthesis, etc. | Checklist ↗ |
| CARE | Case reports | 13-item checklist + timeline of the clinical episode | Checklist ↗ |
| SQUIRE 2.0 | Quality improvement studies | 18 items adapted to iterative, context-dependent interventions | Checklist ↗ |
| GRRAS | Reliability & agreement studies | 15 items for kappa/ICC studies | Checklist ↗ |
The EQUATOR Network (equator-network.org) indexes all of these plus 600+ extensions — search there when your design is unusual.
How to use a reporting guideline well
Pick the guideline at the DESIGN stage, not at submission. The checklists encode what reviewers will ask ("how was the sample size determined?", "who did the interviews and what was their relationship to participants?") — knowing the items before data collection prevents unreportable gaps, like a trial with no registered protocol or a qualitative study that never recorded saturation decisions.
At submission, most journals want the checklist as a supplementary file with page numbers for each item. Fill it honestly: "not applicable" and "not done" are acceptable entries; vague page ranges spanning the whole manuscript are the reviewer red flag.
Guidelines are floors, not ceilings — CONSORT compliance does not make a trial good, it makes a trial’s quality visible. Combine the right checklist with your field’s methodological expectations.
Frequently asked questions
My study mixes methods — which checklist do I use?
Do I need PRISMA for a narrative literature review?
Where do I find extensions like CONSORT for pilot studies?
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