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The CONSORT statement is made up of a 25-item checklist that provides the author with a solid backbone around which to construct and present an RCT. It sets standards on the trial's design, analysis, and interpretation of the results.

The guidance, known as the Consolidated Standards of Reporting Trials (CONSORT) Statement, was first published in 1996 and revised in 2001. It includes a checklist to help authors write reports of randomized controlled trials so that others can judge the reliability and validity of the results.

3 - Method: it should be carefully reported as follows: trial design; eligibility criteria for participants, with explanation of rationale for such criteria; how and where data were collected; thorough description of intervention, which allows results to be reproduced; description of sample size calculation; changes ...

The CONSORT Statement, most recently updated in March 2010, is an evidence-based minimum set of recommendations including a checklist and flow diagram for reporting RCTs and is intended to facilitate the complete and transparent reporting of trials and aid their critical appraisal and interpretation.

Clearly describing this information in the text and in flow diagrams will allow readers to evaluate the applicability of the trial results and facilitate replication. Authors should describe the different types of consent sought and obtained for the cohort or routinely collected database, and the trial.

The CONSORT 2010 Statement is this paper including the 25 item checklist in the table​ and the flow diagram​. It provides guidance for reporting all randomised controlled trials, but focuses on the most common design type—individually randomised, two group, parallel trials.

CONSORT is a protocol developed by a group of researchers not only to identify problems arising from conducting RCTs, but also to report, in a full and clear manner, the results yielded by research, thereby facilitating RCTs reading and quality assessment.

CONSORT stands for Consolidated Standards of Reporting Trials. Its main purpose is to improve the transparency and accuracy of reporting and interpreting the study results from a clinical trial. The initial version was proposed in 1996, and the most updated version was published in 2010.

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Form Packages
Adoption
Bankruptcy
Contractors
Divorce
Home Sales
Employment
Identity Theft
Incorporation
Landlord Tenant
Living Trust
Name Change
Personal Planning
Small Business
Wills & Estates
Packages A-Z
Form Categories
Affidavits
Bankruptcy
Bill of Sale
Corporate - LLC
Divorce
Employment
Identity Theft
Internet Technology
Landlord Tenant
Living Wills
Name Change
Power of Attorney
Real Estate
Small Estates
Wills
All Forms
Forms A-Z
Form Library
Customer Service
Terms of Service
DMCA Policy
About Us
Blog
Affiliates
Contact Us
Privacy Notice
Delete My Account
Site Map
All Forms
Search all Forms
Industries
Forms in Spanish
Localized Forms
Legal Guides
Real Estate Handbook
All Guides
Prepared for You
Notarize
Incorporation services
Our Customers
For Consumers
For Small Business
For Attorneys
Our Sites
US Legal Forms
USLegal
FormsPass
pdfFiller
signNow
airSlate workflows
DocHub
Instapage
Social Media
Call us now toll free:
1-877-389-0141
As seen in:
  • USA Today logo picture
  • CBC News logo picture
  • LA Times logo picture
  • The Washington Post logo picture
  • AP logo picture
  • Forbes logo picture
© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232