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Describing Methods that Let Others Replicate Your Study

  • Rockwood Medical Writing Agency
  • Jul 23
  • 5 min read
Describing Methods that let others replicate your study

The methods section of a scientific paper is more than a technical requirement. It is a statement of transparency and scientific integrity. A well-written methods section allows other researchers to evaluate, reproduce, or build upon your work. Reproducibility is a cornerstone of credible science, and the ability of others to repeat a study hinges on the clarity and completeness of the methodological description.


Aspiring scientists often underestimate the importance of the methods section. There can be a temptation to rush through it or to assume that standard procedures are understood without elaboration. This approach weakens the scientific value of the paper and invites scepticism. A complete and precise account of how the research was conducted is essential.



The Purpose of the Methods Section

The primary goal of the methods section is to explain how the study was performed. This includes the design, setting, participants or materials, procedures, tools, and statistical analysis. The section must be detailed enough that a competent researcher in the same field could repeat the study under similar conditions.


Transparency in reporting methods ensures that the results are credible and that conclusions are grounded in repeatable evidence. Without an adequate methods section, even the most compelling results may lack scientific value.



Structure and Subheadings

The methods section is usually organised into several subheadings. The choice of subheadings depends on the type of research. For a clinical trial, common subheadings include Study Design, Participants, Interventions, Outcomes, and Statistical Analysis. For a laboratory experiment, common headings might include Materials, Sample Preparation, Procedures, and Data Analysis.


Using subheadings improves readability and helps reviewers and readers navigate the section. Follow the conventions of your discipline or the guidance provided by your target journal.



Study Design

Begin by describing the overall design of the study. This might be experimental, observational, prospective, retrospective, cross-sectional, or another recognised type. Specify whether the study is randomised, blinded, controlled, or comparative.


Example:

“This study employed a prospective, double-blind, placebo-controlled design to evaluate the efficacy of Drug X in reducing systolic blood pressure.”


Clearly identifying the study design helps readers understand the level of evidence and potential biases involved.



Setting and Participants

Describe the context in which the study took place. This includes the location, institutional setting, and time frame. Then provide a detailed account of how participants were selected.


Include information on:

  • Inclusion and exclusion criteria

  • Recruitment methods

  • Sample size and justification

  • Consent procedures

  • Ethical approvals


Example:

“Participants were recruited from two urban hospitals between January and June 2023. Eligible individuals were adults aged 40–65 with a diagnosis of stage 1 hypertension. Informed consent was obtained from all participants. The study protocol was approved by the institutional review board at both sites.”


If animals or cell lines were used, provide species, strain, source, and housing conditions. For laboratory studies, describe how specimens were obtained and prepared.



Interventions and Procedures

Describe any interventions, treatments, or protocols in detail. Explain how they were administered, how long they lasted, and under what conditions. If laboratory procedures were used, describe each step clearly, including reagents, concentrations, equipment, and calibration methods.


Avoid vague terms such as “standard procedure” or “usual care” unless those are well-defined within the field. Even when standardised methods are used, include references and clarify any modifications.


Example:

“Blood pressure was measured using a calibrated automated sphygmomanometer (Omron HEM-907). Measurements were taken in triplicate at five-minute intervals, following a 10-minute seated rest.”


Reproducibility depends on detail. Small differences in procedure can lead to significant variation in results.



Materials and Equipment

List all critical materials, instruments, and software used in the study. Include manufacturer names, model numbers, and locations. For software, include version numbers.


Example:

“Genomic DNA was extracted using the QIAamp DNA Mini Kit (Qiagen, Hilden, Germany). Sequencing was performed on the Illumina MiSeq platform (v3, 600-cycle kit). Data analysis was conducted using R software (version 4.2.0).”


If custom tools, devices, or software were used, describe them thoroughly and provide access to design files or source code if applicable.



Outcome Measures

Clearly define the primary and secondary outcomes of the study. State how each was measured, at what time points, and using what instruments or scoring systems.


If subjective measures were used, describe efforts to reduce bias such as blinding or independent assessment. If scales or questionnaires were used, include information about their validity and reliability.


Example:

“Depressive symptoms were assessed using the Patient Health Questionnaire-9 (PHQ-9), administered at baseline, week four, and week eight. A score of 10 or higher was considered indicative of moderate depression.”



Statistical Analysis

Describe the statistical methods used to analyse the data. Include information about:

  • Software and version

  • Tests applied (e.g., t-test, ANOVA, regression)

  • Handling of missing data

  • Criteria for statistical significance

  • Adjustments for multiple comparisons if applicable


Example:

“Continuous variables were compared using independent t-tests. Categorical variables were analysed using chi-square tests. Multivariate logistic regression was used to adjust for age, sex, and baseline blood pressure. Analyses were performed using SPSS version 27.0. A two-sided p-value less than 0.05 was considered statistically significant.”


Specify whether data were checked for normality and how assumptions for statistical tests were assessed. If a power calculation was performed, include the parameters used.



Replicability Versus Word Limits

Many journals impose strict word limits. This can create tension between brevity and completeness. If the full description of a procedure is too long for the main text, consider including supplemental materials. These may house extended protocols, data dictionaries, or programming scripts.


Avoid removing essential details solely to meet word limits. It is better to refer to supplementary information than to leave critical methods vague or omitted.



Ethical Considerations

For studies involving human participants, animal subjects, or sensitive data, include ethical approvals and compliance with relevant guidelines. Mention the review board or ethics committee that approved the study and provide reference numbers where applicable.


Example:

“The study was approved by the Regional Ethics Committee for Human Research (approval number RECH-2023-042). All participants gave written informed consent.”


Adherence to ethical principles reinforces the credibility of the research and protects participants’ rights.



Common Pitfalls to Avoid

  • Insufficient detail: Omitting information may render the study irreproducible.

  • Overreliance on references: Describing a method solely by citing another paper does not suffice unless the procedure is fully standardised.

  • Ambiguous terms: Words like “approximately” or “standard conditions” should be clarified.

  • Lack of consistency: Ensure methods align with what is described in the results and discussion.



Final Thoughts

The methods section reflects the scientific rigour of your study. It should be written with care, precision, and full transparency. Readers should finish the section with a clear understanding of how the research was conducted and with enough information to replicate it if necessary.


Before finalising the methods section, ask a colleague to review it. If they cannot understand or repeat the study based on what is written, revisions are needed. Attention to detail in the methods section signals professionalism and strengthens the integrity of your work.


Scientific research gains value through reproducibility. By writing a thorough and transparent methods section, you contribute not only to your own credibility but also to the advancement of science as a whole.


Contact us if you need expert support with writing or refining your scientific manuscript.


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