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Related Concept Videos

Clinical Trials: Overview01:11

Clinical Trials: Overview

Clinical development focuses on how the drug will interact with the human body and encompasses four key phases of clinical trials, each serving a specific purpose in assessing the safety and effectiveness of new drugs. These phases overlap and build upon one another. Phase I involves a small group of healthy volunteers (typically 20-80 individuals) or, in cases where significant toxicity is expected, patients with the targeted disease, such as cancer or AIDS. The volunteers are tested for...
Clinical Trials01:16

Clinical Trials

Clinical trials are prospective experimental studies conducted on humans to determine the safety and efficacy of treatments, drugs, diet methods, and medical devices. Using statistics in clinical trials enables researchers to derive reasonable and accurate conclusions from the collected data, allowing them to make wise decisions in uncertain situations. In medical research, statistical methods are crucial for preventing errors and bias.
There are four phases in a clinical trial. A phase one...
Types of Reports II: Incident or Occurrence Report01:21

Types of Reports II: Incident or Occurrence Report

An Incident or Occurrence Report in a healthcare setting is a crucial document used to record any unexpected occurrence that may or may not have affected a patient, employee, or visitor. Such reports are critical to improving patient safety and include all details leading up to and including the event.
Purposes:
In the healthcare industry, reports play a crucial role in documenting incidents within an agency. The primary objective of these reports is to ensure patient safety, uphold the...
Blinding01:11

Blinding

Blinding is a commonly used method of not telling participants which treatment a subject is receiving. Blinding is a critical part of a randomized control trial or RCT. It reduces the bias that affects the results. In an RCT, blinding is used in the form of a placebo. A placebo effect occurs when untreated subjects falsely believe they have received the treatment and report improved symptoms. A placebo or a dummy treatment is administered to subjects to negate the bias caused by such an effect.
Introduction to Documentation and Reporting01:20

Introduction to Documentation and Reporting

Documentation is the systematic process of formally recording, maintaining, and communicating information.
Nursing documentation records essential information and details regarding a patient's care and treatment in written or electronic form. It is a critical aspect of nursing practice that involves documenting assessments, interventions, outcomes, and other relevant details about a patient's health status.
Documentation maps the patient's health journey by creating a comprehensive and precise...
Types of Reports III: Telephone and Verbal Reports01:26

Types of Reports III: Telephone and Verbal Reports

Telephone and Verbal Reports in healthcare settings are two communication methods for conveying therapeutic instructions from healthcare providers to nurses or other healthcare staff.
Here's an overview of each type:
Telephone Orders

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Related Experiment Video

Updated: May 9, 2026

Using Visual and Narrative Methods to Achieve Fair Process in Clinical Care
14:32

Using Visual and Narrative Methods to Achieve Fair Process in Clinical Care

Published on: February 16, 2011

Transparent reporting of trials is essential.

Douglas G Altman1

  • 1Centre for Statistics in Medicine, University of Oxford, Oxford, UK. doug.altman@csm.ox.ac.uk

The American Journal of Gastroenterology
|August 6, 2013
PubMed
Summary

Clear reporting of randomized controlled trials (RCTs) is crucial for patient care and research. Adhering to the CONSORT Statement ensures transparency and maximizes the value of clinical trial findings.

Area of Science:

  • Clinical Research Methodology
  • Evidence-Based Medicine

Background:

  • Randomized controlled trials (RCTs) are vital for informing clinical practice and patient care.
  • Effective use of RCTs relies on clear, transparent, and complete reporting of methods and findings.

Purpose of the Study:

  • To emphasize the importance of high-quality reporting for randomized controlled trials (RCTs).
  • To highlight the negative consequences of poor RCT reporting on clinical practice, research, and policy.

Main Methods:

  • Discussion of the essential elements for adequate reporting of randomized controlled trials (RCTs).
  • Reference to the CONSORT Statement as a minimum standard for RCT reporting.

Main Results:

  • Poor reporting of RCTs is a common issue with significant negative impacts.

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  • Adherence to reporting guidelines like the CONSORT Statement is essential for reliable trial interpretation.

    • Conclusions:

    • Authors, peer reviewers, and editors must ensure RCT reports are clear, transparent, and complete.
    • Improving RCT reporting maximizes the value of research investments and benefits patient care.