Title page and manuscript text file should be separately submitted online via the online submission system.
1- Summary (for busy authors)
Title page, including title of the article, authors' names and ORCIDs, affiliations, and detailed information of corresponding authors; Phone and Fax number, Email, and Postal Address should be supplied and submitted as a separate file.
Manuscript text files should be prepared according to specific research reporting guidelines. In addition, declaration section including acknowledgment, funding, authors' contribution, and abbreviations should be addressed at the end of the manuscript text in all types of the articles. All clinical trials should be registered in a registry of clinical trials approved by the World Health Organization (WHO) or the International Committee of Medical Journal Editors (ICMJE). As an option, the Iranian Registry of Clinical Trials (IRCT) or https://clinicaltrials.gov/ct2/home are some of the suggested registries.
The journal adheres to the recommendations of International Committee of Medical Journal Editors (ICMJE). The main manuscript should carry the title, abstract, main text, acknowledgment, funding, authors' contribution, abbreviations, references, figures, and tables of the paper. The preferred word processing format for the manuscript file is Microsoft Word version 2003 or newer. Manuscripts should be double-spaced, with 2.5 cm margins on all sides. All abbreviations must be spelled out the first time used, followed by the abbreviated form in parentheses. Units of measurement must have complied with the International System of Units (SI). For indexing, three to five keywords should be typed at the end of the abstract for each manuscript. These words should be identical to the medical subject headings (MeSH) that appear in the Index Medicus of the National Library of Medicine.
Cohort, case-control, and cross-sectional studies should be arranged based on Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement and checklist as: Abstract, 3-5 Keywords, Introduction, Methods, Results, Discussion, Conclusion, Acknowledgements, References, and maximum 4 Tables and 4 Figures.
A structured abstract (with the subheadings title, Background, Aims, Methods, Results, and Conclusion) should appear on the first page of the manuscript and should not exceed 400 words (250-400 words).
The main text (excluding the abstract, references, figures and tables) should not exceed 3500 words (2500-3500 words). Also, 20-35 references should be stated for original articles.
Original research papers that report a randomized controlled trial, should comply with the guidelines provided by the Consolidated Standards of Reporting Trials (CONSORT) group. In addition, supplying the manuscript with a CONSORT flowchart diagram is highly encouraged. Researchers who would like to publish their clinical trial reports in Novelty in clinical Medicine are strongly encouraged to register their studies in a registry of clinical trials, which meets the criteria of WHO or ICMJE. As an option, the Iranian Registry of Clinical Trials (IRCT) or https://clinicaltrials.gov/ct2/home are some of the suggested registries.
A structured abstract (with the subheadings title, Background, Aims, Methods, Results, and Conclusion) should not exceed 400 words (250-400 words).
The main text (excluding the abstract, references, and maximum 4 tables and 4 figures) should not exceed 3500 words (2500-3500 words). Also, 20-35 references should be stated for original articles.
Narrative Review articles should be composed of systematic critical assessments of literature and data sources pertaining to clinical topics of police medicine, emphasizing factors such as cause, diagnosis, prognosis, therapy, or prevention. They should have unstructured abstracts. All articles and data sources should include information about the specific types of study or analysis, population, intervention, exposure, and tests or outcomes. Authors of review articles should be experts and have contributions in the field of the addressed subject. Narrative reviews should contain at least 60 references. Abstract should be non-structured. The word count should not exceed 4500 words.
Systematic reviews and meta-analyses on clinical trials and observational studies should be prepared based on Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) and Meta-analysis of observational studies in epidemiology (MOOSE), respectively. Systematic reviews and meta-analyses should contain at least 50 references. Abstract should be structured. The word count should not exceed 4500 words.
Case reports should be arranged in accordance with Consensus-based Clinical Case Reporting (CARE) as follows: Abstract (structured, not exceeding 200 words), Introduction, Case Report, Discussion, References, and maximum 1 table and 3 figures. The length should not exceed 1500 words and 10-15 references should be stated.
Original research papers can also be published in a brief format. Submitted papers that are of interest but not acceptable as a full-length original/research article, are offered by the editor to be published in this section. The authors can also primarily submit their papers for consideration for publication in this section. An structured abstract no longer than 200 words is required for this section. The body of the manuscript should not exceed 1500 words. The number of tables and/or figures should be limited to 2 and references to a maximum of 15.
Letters to the Editor/ Editorial
All correspondence will be considered for publication if it contains constructive criticism on previously published articles in Novelty in Clinical Medicine, the authors of which will have the right to reply. In addition, reports of limited research or clinical experiences can be submitted in the form of a letter. The length should not exceed 1000 words. Up to 5 references should be stated.
Reporting Guidelines for Specific Study Designs
Type of Study
Observational studies including cohort, case-control, and cross-sectional studies
Randomized controlled trials
Quality improvement projects
Systematic reviews and meta-analyses
Studies of diagnostic accuracy
Clinical Practice Guidelines
The reporting guidelines for other type of studies can be found at https://www.equator-network.org/reporting-guidelines/.
Based on the ICJME recommendations "all those designated as authors should meet all four criteria for authorship, and all who meet the four criteria should be identified as authors. Those who do not meet all four criteria should be acknowledged". Author's contribution should be stated in the declaration section. All authors should be accountable for all sections of the manuscript and declare that it is written originally and there is no data fabrication; data falsification includes deceptive manipulation of images and plagiarism.
Any change in authorship (i.e. order, addition, and deletion of authors) after initial submission must be approved by all authors via written confirmation, in line with COPE guidelines. It is the corresponding author’s responsibility to ensure that all authors confirm they agree with the proposed changes. If there is disagreement amongst the authors concerning authorship and a satisfactory agreement cannot be reached, the authors must contact their institution(s) for a resolution. It is not the journal editor’s responsibility to resolve authorship disputes. A change in authorship after publication of an article can only be amended via publication of an Erratum.
Funding and Support
All funding sources supporting the work must be declared in the declaration section at the end of the manuscript. Whole affiliations with or financial involvement in any organization on entity with a direct financial interest in the subject matters or materials of the research discussed (examples: employment, consultancies, stock ownership or other equity interest, patent-licensing arrangements) should be cited as a conflict of interest at the end of the manuscript text file.
Conflict of Interest
Authors are expected to disclose any commercial associations or sources of support that might pose a conflict of interest regarding the submitted article.
Author(s) should guarantee that data of the study are available and will be provided if anyone needs them.
Figures and tables
Figures and tables should be kept to a minimum necessary and presented in the manuscript file, numbered (with Arabic numbers), and have a title. Include double-spaced legends (maximum length, 60 words) on separate pages.
Responsibility and ethical requirements
Author(s) should certify that neither the submitted manuscript nor another one with substantially similar content under their authorship has been published in any language or being considered for publication elsewhere. Author(s) should take responsibility for the integrity of the work as a whole, from inception to published article. In the event that an author is added or removed from the list of authors, written acceptance, signed by author(s), must be submitted to the editorial office. Sources of financial support for the project should be acknowledged. If the study involves human beings, the author(s) must include a statement that the study was approved by the local ethical committee and that written informed consent was obtained from the study participants. For those who do not have formal ethics review committees, the principles outlined in the Declaration of Helsinki should be followed. Also, the compliance of maintenance and care of experimental animals with National Institutes of Health guidelines for the human use of laboratory animals should be declared in the text. All relevant permissions to use unpublished observations of others must be obtained by the manuscript author(s) and stated in the text citing the names of the original author(s) should be declared. Also, permission must be obtained to reproduce or adapt any figures or tables that have been published previously and declared in the legend/footnote. Novelty in clinical Medicine conforms to the international regulations against scientific misconduct including fabrication, falsification, plagiarism, and etc. In Novelty in clinical Medicine any cases of suspected misconduct will be assessed during the peer-review and publication process based on COPE guidelines.
The editor in chief makes the final decision regarding the publication or rejection of the submitted articles without interference from its owner or economic interests.
Article submission, processing, acceptance, and publishing in this journal are free.