STROBE/CONSORT Methods-Results Writer
Writes with the standard that fits your study type
STROBE/CONSORT Methods-Results Writer
Writes with the standard that fits your study type
Description
Produces a complete Methods + Results section following the reporting standard that fits your study design (STROBE for observational studies, CONSORT for randomized controlled trials); then audits which checklist items are missing or weakly reported without concealment, and suggests how to complete them. Who it's for: researchers seeking reporting robustness before journal submission and graduate students writing a thesis.
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Shuting@YouMind
Why we love this skill
An editor-minded reporting partner that selects STROBE or CONSORT based on study design, drafts publication-ready Methods and Results, and audits every checklist item. It stands out by exposing weak reporting, requiring confidence intervals, and enforcing appropriately cautious causal language.
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Related Skills
View allSTROBE Methods Writer
Based on your cross-sectional, cohort, or case-control study design; when you enter your participant selection method, variables, sample size rationale, and statistical methods, it produces a complete Methods and Results draft with implicit reference to all 22 items of the STROBE (Strengthening the Reporting of Observational Studies in Epidemiology) checklist. It also provides a mapping table at the end showing which paragraph corresponds to which STROBE item — ready to answer a journal's "please complete the STROBE checklist" request. Avoids causal language (uses "is associated with" rather than "causes" for observational studies) and explicitly discusses sources of bias/confounding. Suitable for academics working in epidemiology, public health, and clinical research.
Qualitative Rigor & COREQ Auditor
Writes a Methods section based on Lincoln & Guba's trustworthiness criteria from your qualitative study design; then reveals which COREQ checklist items are missing or weakly reported, without concealment. Who it's for: researchers seeking reporting robustness before journal submission and graduate students writing a thesis.
CONSORT 2010 Report Writer
From your randomized controlled trial (RCT) data — randomization method, blinding status, power analysis, CONSORT flow numbers (screened/randomized/allocated/analyzed), ITT/PP analysis approach — it produces a complete Abstract + Methods + Results draft compliant with all 25 items of CONSORT 2010. It never confuses ITT/PP; it checks the consistency of flow diagram numbers (randomized ≥ allocated ≥ followed-up ≥ analyzed). It also pre-identifies at least 4 objections journal reviewers frequently raise (e.g., "why wasn't an ITT analysis reported," "was blinding success tested," "was there outcome switching") and suggests a defense sentence for each. Designed for clinical researchers in medicine/nursing/pharmacy conducting RCTs who want methodological robustness before journal submission. What it does not do: it does not perform statistical analysis or generate data — it only converts results you already have into a CONSORT-standard report.
