Related Experiment Video
Updated: May 16, 2026

Working with Human Tissues for Translational Cancer Research
Published on: November 26, 2015
[Analysis of informed consent readibility in intensive care]
M R Ramírez-Puerta1, R Fernández-Fernández, J C Frías-Pareja
1Servicio de Medicina Intensiva, Hospital Universitario San Cecilio, Granada, España.
Informed consent documents in intensive care and the Andalusian Healthcare System are largely unreadable. Most documents failed readability tests, hindering patient understanding and the effectiveness of informed consent.
Area of Science:
- Medical Ethics
- Health Communication
- Patient Advocacy
Background:
- Informed consent is crucial for patient autonomy in healthcare.
- Readability of informed consent documents directly impacts patient comprehension and decision-making.
- Previous assessments indicate challenges in simplifying complex medical information for diverse patient populations.
Purpose of the Study:
- To evaluate the readability of informed consent (IC) documents used in an intensive care unit (ICU) and across the Andalusian Healthcare System (AHS).
- To identify specific readability metrics that are not met by current IC documents.
- To inform improvements in patient communication and understanding of medical procedures.
Main Methods:
- A descriptive study analyzing 14 IC documents from an ICU and 14 from the AHS.
- Utilized six readability scores: Flesch, Sentence complexity, LEGIN, Fernández-Huerta, Szigriszt, and INFLESZ.
- Quantified the percentage of documents meeting each readability criterion.
Main Results:
- A significant majority of IC documents (85.7%) failed to meet at least one readability index.
- Only 14.3% of documents satisfied all analyzed readability indexes.
- While some scores showed better performance (e.g., Sentence complexity), overall readability remains a concern across both ICU and AHS settings.
Conclusions:
- Informed consent documents analyzed are generally difficult for the public to read and comprehend.
- The current IC documents do not effectively fulfill their primary purpose of ensuring clear patient understanding.
- There is a critical need to revise and simplify IC documents to enhance patient comprehension and uphold ethical standards.
More Related Videos
10:38Observational Study Protocol for Repeated Clinical Examination and Critical Care Ultrasonography Within the Simple Intensive Care Studies
Published on: January 16, 2019
06:28E-Patient Counseling Trial (E-PACO): Computer Based Education versus Nurse Counseling for Patients to Prepare for Colonoscopy
Published on: August 1, 2019
Related Concept Videos
Nurses' Legal Responsibilities I
The legal responsibilities of a nurse regarding informed consent include the following:
Nursing Ethical Principles II
Consider the following scenario, which illustrates how these principles are applied in the care of Mr. John, a fifty-year-old teacher diagnosed with metastatic liver cancer.
Initially, Mr. John's cancer...
Types of Biopharmaceutical Studies: Controlled and Non-Controlled Approaches
Non-controlled studies, commonly employed for initial exploration, lack a control group, rendering them susceptible to biases and external influences. In contrast, controlled...
Bioavailability Study Design: Healthy Subjects Versus Patients
Methods of Documentation III: PIE
Obedience