Transparency
Manuscripts should clearly report what was planned, what was done, what was found and what limitations may affect interpretation.
UnivColl Publications encourages authors to use appropriate reporting guidelines and checklists so that manuscripts are complete, transparent, verifiable and easier for editors, reviewers, readers and institutions to assess.
Reporting guidelines are not a substitute for scientific quality, but they help authors present research in a structured and transparent way. They also help editors and reviewers identify missing details in study design, methods, analysis, results, ethics, funding, conflicts and data availability.
This policy supports use of internationally recognised and discipline-specific reporting guidance where relevant, including guideline families for trials, systematic reviews, observational studies, case reports, qualitative research, animal studies, diagnostic accuracy, prediction models, quality improvement, economic evaluation and AI-related studies.
Publisher DOI Prefix: 10.65919 | Connecting University & College Research Worldwide
Study design, checklist, ethics, data, funding, conflicts, AI use and peer review readiness.
Reporting guidance helps improve manuscript clarity without replacing editorial or peer review judgement.
Manuscripts should clearly report what was planned, what was done, what was found and what limitations may affect interpretation.
Authors should include essential information required for editors, reviewers, readers and future researchers to understand the study.
Reporting guideline selection should match the actual study design, such as trial, review, observational study, case report or qualitative research.
Methods, data availability, materials, analysis approach and decision rules should be reported in a way that supports verification and responsible reuse.
Ethical approval, consent, funding, conflicts, AI use, authorship and data statements should be disclosed where relevant.
Use of a reporting checklist supports completeness but does not guarantee acceptance, indexing, DOI assignment or editorial approval.
The correct guideline depends on study type, discipline and manuscript purpose.
Authors should report trial design, participants, interventions, outcomes, allocation, analysis and participant flow where applicable.
Authors should report protocol design, trial planning, interventions, outcomes, ethics and registration where applicable.
Authors should report search strategy, selection process, eligibility criteria, included studies, synthesis method and flow diagram where applicable.
Authors should report design, setting, participants, variables, bias, sample size, statistical methods and results clearly.
Authors should report patient/context details, timeline, diagnostic assessment, intervention, outcomes and consent where applicable.
Authors should report research team, reflexivity, sampling, data collection, coding, analysis, themes and trustworthiness.
Authors should report animal details, study design, sample size, experimental procedures, randomisation, blinding and welfare where applicable.
Authors should report participants, index test, reference standard, diagnostic accuracy estimates and study flow where applicable.
Authors should report data source, predictors, outcomes, model development, validation, performance and limitations.
Authors should report problem, context, intervention, study of intervention, measures, results and interpretation.
Authors should report perspective, comparators, time horizon, costs, outcomes, assumptions and uncertainty.
Authors should report data source, model development, validation, performance, bias, transparency, limitations and human oversight where applicable.
Authors should use recognised field-specific reporting norms, methodological transparency and journal instructions.
Authors should clearly label abstract, full paper, proceedings paper or expanded article and avoid duplicate publication confusion.
Authors should report objective, approach, source selection, argument structure, limitations and contribution transparently.
Authors should select the guideline that matches the actual study design, not the preferred publication label.
| Manuscript Type | Suggested Guideline | Minimum Check |
|---|---|---|
| Randomized trial | CONSORT / relevant CONSORT extension | Trial design, participant flow, allocation, outcomes, harms and open-science disclosures where applicable. |
| Trial protocol | SPIRIT | Protocol items, intervention details, outcomes, ethics, registration and analysis plan. |
| Systematic review or meta-analysis | PRISMA | Search, eligibility, selection, flow diagram, synthesis method, risk of bias and funding. |
| Observational study | STROBE | Design, setting, participants, variables, bias, sample size and statistical methods. |
| Case report | CARE | Case details, timeline, diagnosis, intervention, outcomes, patient/participant consent where applicable. |
| Qualitative study | COREQ or SRQR | Sampling, researcher role, data collection, analysis, themes, trustworthiness and ethics. |
| Diagnostic accuracy study | STARD | Index test, reference standard, participant flow and diagnostic accuracy estimates. |
| Prediction model / AI study | TRIPOD / AI extensions or suitable ML reporting guidance | Data source, model, validation, performance, bias, explainability and limitations. |
| Quality improvement study | SQUIRE | Problem, context, intervention, measures, results and sustainability. |
| Economic evaluation | CHEERS | Perspective, alternatives, costs, outcomes, time horizon, assumptions and uncertainty. |
Authors are responsible for choosing the correct guideline and ensuring the manuscript reports essential information.
Identify the manuscript study design before submission
Select the most suitable reporting guideline or checklist
Upload or provide checklist when requested by the journal
Report essential methods and results completely
Explain why a checklist item is not applicable where relevant
Include ethical approval and consent statements where applicable
Disclose funding, conflicts of interest and sponsor role
Disclose AI use where relevant to writing, analysis or interpretation
Report data availability and material availability where applicable
Avoid selective reporting or omission of negative/inconclusive findings
Use transparent tables, figures and flow diagrams where relevant
Ensure title and abstract accurately reflect study design
Check references and prior literature claims
Avoid plagiarism, duplicate submission and redundant publication
Use correct version labels for preprint or conference versions
Respond to editorial requests for missing reporting items
Editors and reviewers may use reporting guidelines to identify missing details and improve manuscript transparency.
Check manuscript type and study design
Check whether a suitable reporting guideline has been used
Check title, abstract and methods for design clarity
Check ethics, consent, funding, conflicts and AI disclosure
Check data availability and material availability statements
Check review articles for search and selection transparency
Check trial and intervention studies for participant flow and outcomes
Check observational studies for sample, variables, bias and statistics
Check qualitative studies for sampling, data collection and analysis transparency
Check case reports for consent and timeline clarity where applicable
Request checklist revision if essential information is missing
Do not use checklist completion as automatic acceptance
These basic items are useful across most research manuscripts, in addition to study-design-specific guidelines.
A clear workflow helps authors, editors and reviewers handle reporting requirements without confusion.
Author identifies whether the manuscript is a trial, observational study, review, case report, qualitative study, AI study or other type.
Author selects the most relevant checklist or reporting standard based on study design and subject area.
Author ensures the manuscript includes essential reporting items and prepares a checklist when requested.
Editor checks basic completeness, study design clarity, disclosure statements and guideline suitability.
Reviewers may use the selected guideline to assess completeness, transparency and missing reporting details.
Author revises missing items and the editorial office checks final reporting, metadata and disclosures before publication.
Missing reporting items may lead to request for clarification, revision or rejection depending on seriousness.
| Situation | Risk | Possible Action |
|---|---|---|
| Relevant checklist is complete and manuscript is transparent | Low | Proceed with normal editorial or peer review workflow. |
| Checklist is missing but manuscript type requires it | Medium | Request checklist before or during review. |
| Wrong reporting guideline used | Medium | Ask author to use correct guideline and revise reporting. |
| Essential method details missing | Medium to high | Return for revision or reject if transparency is insufficient. |
| Ethics or consent statement missing where required | High | Request clarification; do not proceed without adequate ethics handling. |
| Systematic review lacks search and selection transparency | High | Request PRISMA-style reporting revision or decline. |
| AI or machine learning study lacks data/model transparency | High | Request detailed data, validation, bias and limitation reporting. |
| Checklist completed mechanically but paper has quality problems | Medium | Continue scientific and editorial assessment; checklist alone is not acceptance. |
Reporting guidelines should improve transparency, not become a box-ticking exercise or a way to hide weak reporting.
Submitting a checklist without actually reporting the required items
Using the wrong guideline to avoid required transparency
Omitting negative or inconvenient results
Claiming review completeness without search strategy
Hiding sample selection, missing data or exclusions
Reporting trial results without participant flow where applicable
Reporting case details without required consent where applicable
Using AI-generated methods or results without disclosure
Changing study design label to avoid reporting requirements
Treating checklist completion as publication guarantee
Ignoring ethics, consent, funding or conflict statements
Misrepresenting conference abstract as full peer-reviewed article
Using unverifiable data, figures or fabricated results
Refusing reasonable editorial requests for missing reporting details
Reporting guidelines connect directly with author instructions, peer review, ethics, data and AI policies.
Author-facing instructions for manuscript preparation, structure and submission requirements.
Open PageHow reviewers and editors assess manuscripts and reporting completeness during peer review.
Open PageResearch integrity, misconduct prevention, transparency and ethical reporting expectations.
Open PageData availability, materials, transparency and responsible research record support.
Open PageAI disclosure, limitations and responsible reporting when AI tools are used.
Open PageForms, checklists, templates and author declaration documents.
Open PageLater the CMS can track manuscript type, selected guideline, checklist upload, flow diagram, missing items, ethics statements, data statements and editorial checks.
Reporting guideline compliance supports completeness and transparency, but it does not guarantee acceptance, peer review approval, DOI assignment, indexing, citation, publication certificate or external recognition.
Complete reporting helps reviewers focus on scientific quality and helps readers understand what was done, how it was done and how reliable the conclusions may be.
Basic questions about reporting guidelines, manuscript checklists, editorial screening and acceptance expectations.
Reporting guidelines are checklists or structured recommendations that help authors report research methods, results and disclosures completely and transparently.
They may be required or strongly recommended depending on manuscript type, journal instructions and editorial assessment.
Authors should choose the guideline that matches the study design, such as PRISMA for systematic reviews, STROBE for observational studies or CONSORT for randomized trials.
No. A checklist supports transparent reporting but does not guarantee acceptance, DOI assignment, indexing or publication.
Yes. Editors may request a checklist or reporting revision during screening, peer review or revision.
Authors should mark the item as not applicable and briefly explain why it does not apply to the manuscript.
No. Although many established guidelines are used in health research, the principle of transparent and complete reporting is useful across disciplines.
No. Guidelines support completeness checks, but scientific quality, originality, ethics and relevance still require editorial and peer review assessment.
This policy is connected with UnivColl Publications' wider publishing ecosystem, including author guidance, editorial independence, publication ethics, metadata readiness and official support routes. Use the related links to move to the next practical step without relying on disconnected or informal information.
UnivColl Publications uses policy pages to support transparent communication, fair editorial handling, author awareness and scholarly record integrity. Submission, payment, policy compliance or support communication must not be treated as a promise of acceptance, indexing, citation, ranking or any third-party database outcome.
Editorial and publication decisions should remain evidence-based, policy-led and independent.
Acceptance depends on scope, originality, review suitability, ethical compliance and editorial decision.
Published records may be supported with structured metadata, DOI references and correction workflows where applicable.
Queries should include manuscript ID, DOI, transaction reference or policy concern details where available.