Use when verifying trial registration, IRB/ethics approval, informed consent, ICMJE authorship and conflict-of-interest disclosures, and the data-sharing statement for a JAMA manuscript. Confirms compliance; it does NOT design the study or write the abstract.
Scanned 6/5/2026
Install to Claude Code
npx -y skills add brycewang-stanford/Awesome-Journal-Skills --skill jama-ethics-registration --agent claude-codeInstalls into .claude/skills of the current project.
Are you the author of Jama Ethics Registration?
Add the live security badge to your README — it updates automatically with every re-scan.
[](https://www.skillsdirectory.com/skills/brycewang-stanford-jama-ethics-registration)More formats (shields.io, HTML) on the badges page.
---
name: jama-ethics-registration
description: Use when verifying trial registration, IRB/ethics approval, informed consent, ICMJE authorship and conflict-of-interest disclosures, and the data-sharing statement for a JAMA manuscript. Confirms compliance; it does NOT design the study or write the abstract.
---
# Ethics, Registration & Disclosures (jama-ethics-registration)
## When to trigger
- A clinical trial's registration status or timing is uncertain
- IRB/ethics approval or informed-consent statements are missing from Methods
- Author roles, contributorship, or COI disclosures are incomplete
- A data-sharing statement is required and not yet drafted
## Prospective trial registration (ICMJE policy)
- Clinical trials must be **prospectively registered — before the first participant is enrolled** — in ClinicalTrials.gov or another ICMJE-accepted registry (e.g., a WHO ICTRP primary registry).
- A trial registered **after enrollment began** is retrospectively registered; ICMJE journals including JAMA treat this as non-compliant, and it generally cannot be remedied at submission. Disclose it transparently if it happened — do not hide it.
- Report the registry name and trial identifier in the abstract (Trial Registration line), the Methods, and any required submission field.
- Systematic reviews/meta-analyses should register the protocol (e.g., PROSPERO) and cite it.
## Ethics and consent statements (in Methods)
- Name the **IRB / research ethics committee** that approved the study (or state the basis for exemption).
- State that the study followed the **Declaration of Helsinki** (and Good Clinical Practice for trials, as applicable).
- State how **informed consent** was obtained, or justify any waiver.
- For studies with identifiable individuals (including images/case details), obtain and state **consent for publication**.
## ICMJE authorship, contributorship, and disclosures
- Each author should meet the **ICMJE four authorship criteria**; non-qualifying helpers go in Acknowledgments.
- Provide a **contributorship** statement (who did what).
- Every author files an **ICMJE Disclosure of Potential Conflicts of Interest** form; summarize relevant financial and non-financial conflicts in the manuscript.
- Disclose **funding sources** and the **role of the funder/sponsor** (design, conduct, analysis, decision to publish).
- For trials, address **access to data / statistical responsibility** (which authors had full data access and vouch for the analysis).
## Data sharing
- Provide a **data-sharing statement** (per ICMJE) for clinical trials and, increasingly, other study types: whether de-identified individual-participant data will be shared, what documents (protocol, statistical analysis plan), when, with whom, and by what mechanism.
## Checklist
- [ ] Trial prospectively registered before enrollment; registry + ID reported
- [ ] Systematic-review protocol registered (e.g., PROSPERO) and cited
- [ ] IRB/ethics approval (or exemption) named in Methods
- [ ] Declaration of Helsinki (and GCP for trials) stated
- [ ] Informed-consent process described or waiver justified
- [ ] Consent for publication for identifiable individuals
- [ ] All authors meet ICMJE criteria; contributorship statement present
- [ ] COI disclosure forms collected; conflicts summarized
- [ ] Funding source and funder role stated
- [ ] Data-sharing statement drafted
## Anti-patterns
- Unregistered trial, or registration after enrollment began
- "IRB approval obtained" with no committee named
- Honorary/guest authorship; ghostwriting
- Undisclosed industry funding or author conflicts
- Funder controlled analysis or publication decision, undisclosed
- "Data available upon request" used as a non-committal placeholder
## Output format
```
【Trial registration】prospective + ID: ... / retrospective (disclose) / n.a.
【Protocol registration (review)】PROSPERO ID / n.a.
【IRB + Helsinki + consent stated】yes / fixes: ...
【ICMJE authorship + contributorship】complete / issues: ...
【COI + funding + funder role disclosed】yes / gaps: ...
【Data-sharing statement】drafted / missing
【Next skill】jama-writing-style
```
Is this your skill, or is something wrong with this listing? Request removal or report an issue. Author removals are honored within 72 hours.
No comments yet. Be the first to comment!