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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.

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Quantitative designs
GuidelineUse forCore contentChecklist
CONSORT 2010Randomized controlled trials25-item checklist + participant flow diagram (enrollment → allocation → follow-up → analysis)Checklist ↗
SPIRIT 2013Trial protocols33 items for the protocol itself — required by many registries and fundersChecklist ↗
STROBEObservational studies (cohort, case-control, cross-sectional)22 items; separate flavors per design; STROBE-nut, RECORD and other extensions existChecklist ↗
STARD 2015Diagnostic accuracy studies30 items + flow of participants through the index test and reference standardChecklist ↗
TRIPOD 2015 (+AI 2024)Prediction model development/validationModel specification, performance, validation; TRIPOD+AI covers machine-learning modelsChecklist ↗
CHEERS 2022Health economic evaluations28 items covering perspective, discounting, sensitivity analysesChecklist ↗
ARRIVE 2.0Animal (in vivo) research"Essential 10" + recommended set for design, sample size, blindingChecklist ↗
Reviews, qualitative, and other designs
GuidelineUse forCore contentChecklist
PRISMA 2020Systematic reviews & meta-analyses27 items + the flow diagram of records identified → screened → includedChecklist ↗
PRISMA-ScRScoping reviews20-item adaptation of PRISMA for scoping questionsChecklist ↗
MOOSEMeta-analyses of observational studiesSearch, heterogeneity, and bias reporting specific to observational synthesesChecklist ↗
COREQQualitative interviews & focus groups32 items: research team, methods, analysis and reportingChecklist ↗
SRQRQualitative research (any method)21 items; broader and less interview-specific than COREQChecklist ↗
ENTREQQualitative evidence syntheses21 items for meta-ethnography, thematic synthesis, etc.Checklist ↗
CARECase reports13-item checklist + timeline of the clinical episodeChecklist ↗
SQUIRE 2.0Quality improvement studies18 items adapted to iterative, context-dependent interventionsChecklist ↗
GRRASReliability & agreement studies15 items for kappa/ICC studiesChecklist ↗

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?
There is no single dominant mixed-methods guideline; common practice is GRAMMS (Good Reporting of A Mixed Methods Study, 6 items) plus the relevant single-method checklists for each strand (e.g. STROBE for the survey strand, COREQ for the interviews). State this approach explicitly in your methods.
Do I need PRISMA for a narrative literature review?
No — PRISMA presumes a systematic search and screening process. Using it for a narrative review implies rigor that was not applied. Consider the SANRA scale for narrative reviews, or upgrade the review to a scoping review (PRISMA-ScR) if you can make the search systematic.
Where do I find extensions like CONSORT for pilot studies?
The EQUATOR Network library lists them all: CONSORT extensions for pilot/feasibility trials, cluster trials, and non-pharmacological interventions; PRISMA extensions for network meta-analyses, protocols (PRISMA-P), and searching (PRISMA-S). Search by design keyword rather than browsing.

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