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e-Prone Clinical Protocol

e-Prone Clinical Protocol

On this platform you will find information and resources that will enable you to learn about and implement the protocol of the study "Effect of Continuous Prolonged Prone Position versus Intermittent Daily Prone Position on Mortality in ARDS Patients: A Multicenter Randomized Controlled Trial".

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Responsable mpamthau@uc.cl
Última actualización 29/04/2025
Tiempo de finalización 20 minutos
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e-Prone Clinical Protocol

Suggested Model for Informed Consent Request

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Recommendations for Informed Consent Request
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e-Prone Clinical Protocol
Suggested Model for Informed Consent Request

Download the PDF version


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e-Prone Clinical Protocol
Invitation to Participate in the Clinical Study - Case of a Family Member Requesting More Information
The following presents an example of how to carry out the authorization request procedure with the patient's designated family member when additional information is requested or further concerns are raised. English and Spanish subtitles are available and can be activated in the video.
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e-Prone Clinical Protocol
Invitation to Participate in the Clinical Study - Standard Case
Below is a standard example of how to carry out the procedure for requesting authorization from the patient’s legal representative. The video includes English and Spanish subtitles that can be activated.
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