CONSORT 2010 Report Writer
Produces a CONSORT-compliant report from your RCT data
CONSORT 2010 Report Writer
Produces a CONSORT-compliant report from your RCT data
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Description
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.
Recommended by
Shuting@YouMind
Why we love this skill
An editor’s pick for turning raw RCT data into a complete CONSORT 2010 manuscript draft, with internally checked participant-flow logic and clear ITT/PP distinctions. It also anticipates reviewer challenges with ready-to-adapt defenses and flags protocol or outcome-switching risks.
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Generates a complete Abstract + Methods + Results draft from your randomized controlled trial (RCT) data—randomization method, blinding status, power analysis, CONSORT flow counts (screened/randomized/allocated/analyzed), and ITT/PP analysis approach—in accordance with CONSORT 2010’s 25-item checklist. It never confuses ITT and PP; it checks the consistency of flow diagram counts (randomized ≥ allocated ≥ followed-up ≥ analyzed). It also proactively identifies at least 4 objections frequently raised by journal reviewers (such as “Why was an ITT analysis not reported?”, “Was the success of blinding tested?”, and “Was there any outcome switching?”) and suggests a defense sentence for each. Designed for clinical researchers and academics conducting RCTs in medicine, nursing, or pharmacy who want methodological rigor before journal submission.
Information
- Version
- v2
- Last updated
- Runtime credits
- Usage-based
- Models
- Auto
