International Journal of Thorax

International Journal of Thorax

International Journal of Thorax – Instructions For Author

Open Access & Peer-Reviewed

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International Journal of Thorax - Instructions for Authors

Modern, submission ready guidance for fast, fair review

Author Preparation Blueprint

This page is a practical blueprint for preparing manuscripts for the International Journal of Thorax. It is designed to help your research move through peer review quickly with fewer revisions.

Research Focus

Well structured submissions allow reviewers to evaluate clinical relevance, methodological rigor, and patient impact rather than formatting issues.

Why It Matters

We publish original research, reviews, brief reports, methods, and editorials across thoracic and respiratory medicine.

Quality Signals

Use ManuscriptZone or the simple submission form and choose the workflow that best fits your team and institution.

Trust & Integrity

Align with relevant reporting frameworks such as CONSORT, STROBE, PRISMA, CARE, or ARRIVE when appropriate and submit any checklists required by your study type.

Visibility

Include ethics approvals, informed consent statements, and trial registration numbers where required.

Author Support

Describe study design, setting, patient population, and endpoints clearly to strengthen reproducibility and impact.

Data & Access

If your study includes imaging, bronchoscopy, or physiologic testing, report equipment, protocols, and calibration standards.

Method Clarity

Consistency across text, tables, and figures reduces editorial queries and helps production maintain the final record.

Impact

Use clear, concise language for interdisciplinary readers across pulmonology, thoracic surgery, and critical care.

Compliance

If you need guidance on scope or format, contact the editorial office before submitting.

Quick Compliance Panel

  • Title page includes affiliations, ORCID, funding, and contributions
  • Structured abstract with objectives, methods, results, and conclusions
  • IMRAD main text with continuous line numbering
  • Figures at 300 dpi and tables submitted as editable files
  • Ethics approvals, consent statements, and trial registration included when relevant
  • Data availability statement with repository links or access terms
  • Cover letter confirms exclusivity and preprint disclosure
  • Report statistical methods, software versions, and primary outcomes
  • State limitations, safety reporting, and reproducibility steps

Why These Standards Matter

A modern, compliant submission improves review speed, clarity, and credibility.

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Clear Structure

IMRAD format, structured abstracts, and logical headings improve readability and reduce reviewer friction.

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Ethics and Integrity

Ethics compliance and similarity screening protect the record and author reputation.

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Data Transparency

Data availability statements and repository links strengthen trust, reuse, and citation potential.

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Technical Quality

High resolution images, de identified figures, and editable tables reduce production delays.

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Reviewer Focus

Complete methods and validation keep review centered on scientific value.

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Funder Compliance

Reporting and licensing alignment supports grants, institutional policies, and public access mandates.

Manuscript Preparation Standards

Clear sub sections make your submission easy to review and easier to publish.

Title Page

Title Page

Establish authorship, accountability, and funding transparency.

  • Full author names, affiliations, and ORCID identifiers
  • Corresponding author email and address
  • Funding sources and grant numbers
  • Conflict of interest and author contribution statements
  • Ethics approval identifiers and consent statements when required
  • Clinical trial registration number when applicable
  • Cover letter summarizing novelty and confirming exclusive submission

Abstract

Abstract

Make your work searchable and easy to interpret.

  • Structured abstract for original research manuscripts
  • Clear objectives, methods, results, and conclusions
  • Four to six keywords aligned with indexing terms
  • Include study design, population, and primary outcomes
  • Short, direct sentences that make the study easy to scan

Main Text

Main Text

Provide a complete narrative with reproducible methods.

  • IMRAD structure for original research
  • Clear study design, setting, and participant selection
  • Interventions, outcomes, and follow up described
  • Statistical analysis plan and software reported
  • Use SI units and define abbreviations at first use
  • Include limitations and reproducibility considerations in the discussion
FormattingRequirementNotes
File formatWord (.doc or .docx)Main text in one file, figures separate
Font and spacing12 pt, double spacedUse standard fonts
Line numbersContinuousRequired for review
Trial registrationProvide registry IDIf applicable
Figures300 dpiTIFF, JPEG, or PNG, de identified

Figures and Tables

Figures/Tables

Ensure data presentation is clear and publication ready.

  • Figures at 300 dpi in TIFF, JPEG, or PNG formats
  • Editable tables with titles, footnotes, and units
  • Complete figure legends, scale bars, and imaging parameters
  • Remove patient identifiers and maintain confidentiality
  • Supplementary files cited in the main text
  • Consistent naming so files match order of appearance

References

References

Accurate citations speed production and improve discovery.

  • Vancouver style references
  • DOI links included where available
  • Cite clinical trial registrations and datasets when used
  • Complete and consistent formatting
  • Check for accuracy before submission
  • Include access dates for data when needed

Ethics and Data Callouts

These statements are reviewed early in screening and must be clear at submission.

Ethics

Ethics Statement Required

Provide IRB or ethics committee approvals for human participants or animal studies. Include approval identifiers, dates, and consent statements.

Data

Data Availability Statement Required

State where de identified data are stored, include repository links or accession numbers, and describe any access restrictions or embargoes.

Registration

Trial Registration Required

Clinical trials must be registered in a public registry prior to enrollment. Include the registration number in the abstract.

Submission Pathway

Use this pathway to keep your submission compliant and on schedule.

1

Assemble Core Files

Prepare title page, main manuscript, figures, tables, and supplementary files with clear naming. Confirm that all files are cited in the text.

2

Run Compliance Check

Confirm ethics approvals, consent statements, and data availability. Ensure conflicts and funding are fully disclosed.

3

Apply Technical Formatting

Use Word format, twelve point font, double spacing, and continuous line numbering. Keep headings consistent across sections.

4

Quality Review

Verify study design details, statistical methods, and reference accuracy including DOI links. Check that figures match legends and labels.

5

Submit via Preferred Method

Submit through ManuscriptZone or the simple submission form. Upload figures separately and include a concise cover letter.

6

Post Submission Readiness

Respond quickly to editorial queries and provide marked and clean revisions. Address reviewer feedback point by point.

7

Proof and Publish

Review page proofs carefully for accuracy. Confirm that metadata, author details, and data links are correct. Report any corrections immediately.

Frequently Asked Questions

What are the typical word counts?
Original research is typically 4,000 to 8,000 words, reviews 6,000 to 10,000 words, and brief reports 1,500 to 3,000 words.
Do you accept preprints?
Yes. Disclose preprint posting at submission and update the record after acceptance.
What reporting guidelines are required?
Use CONSORT, STROBE, PRISMA, CARE, ARRIVE, or other relevant guidelines for your study design.
What file formats are accepted for figures?
Submit figures at 300 dpi in TIFF, JPEG, or PNG formats with complete legends.
Is a data availability statement required?
Yes. Every manuscript must include a clear data availability statement.
Can I submit supplementary data?
Yes. Supplementary files are encouraged and must be cited in the text.
Do you screen for similarity?
Yes. All submissions are screened for originality and compliance.
How do revisions work?
Provide a point by point response and submit both marked and clean manuscripts.
Can I suggest reviewers?
Yes. Provide suggested reviewers with relevant expertise and no conflicts of interest.
What is the policy on image manipulation?
Only minimal, clearly disclosed adjustments are allowed. Provide scale bars and original data on request.
Do you require ORCID identifiers?
ORCID is strongly recommended to improve author attribution and indexing accuracy.
Do you require trial registration?
Yes for clinical trials. Include the registry and ID in the abstract.
Can authorship change after submission?
Authorship changes require written approval from all authors and editorial review.
Are replication or benchmarking studies welcome?
Yes. Rigorous studies that validate methods or models are encouraged.
Do you require line numbering?
Yes. Use continuous line numbering to help reviewers and editors reference sections.
Can I deposit code and datasets?
Yes. Use trusted repositories and include accession numbers or persistent links.
Are conference abstracts considered prior publication?
No. Disclose prior abstract presentations in the cover letter and manuscript.
How do you handle restricted data?
Explain restrictions and provide access criteria or summaries where possible.

Important Points

  • Use two submission methods: ManuscriptZone and the simple submission form.
  • Ensure references are accurate and include DOI links where possible.
  • Define all abbreviations in every table and figure.
  • Include ethics approvals, consent statements, and trial registration when required.
  • Provide ORCID identifiers to improve author attribution.
  • Use SI units and standard clinical terminology.
  • Keep file names short, descriptive, and consistent with figure order.
  • Report statistical methods, effect sizes, and confidence intervals clearly.
  • Use continuous line numbering to speed reviewer feedback.
  • Add a running title and corresponding author details on the title page.
  • Confirm that all coauthors approve the submission.
  • Disclose any conflicts of interest and funding sources.

Submit Your Manuscript

Use the submission system below to start your International Journal of Thorax review process.

For assistance, contact us at [email protected]