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Clinical Trial Summary

Our goal is to compare two types of advance directives forms available in English and Spanish to determine which is more easy to use for patients.


Clinical Trial Description

Step1: Any adult participant who is interested in completing advance directives and able to read and write in English and or Spanish will be eligible to participate in the study Step 2: Online Stanford consent form will be presented before the participants. Only after they read the consent and click on the participation link will they be able to enter the study.Those who are willing to participate will be randomly assigned to either the letter or traditional advance directives in Spanish and study measures. They will also answer questions as to how much they liked and understood the documents. Step 4: The investigators will collect data until the investigators reach an n=1000 Step 5: The investigators will analyze the results and submit for publication. In this protocol, we are assessing whether patients prefer the traditional advance directives or the letter directive. As it is just an questionnaire based study, there no risk for patients. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02799537
Study type Interventional
Source Stanford University
Contact VJ Periyakoil, MD
Phone (650) 493-5000
Email Periyakoil@stanford.edu
Status Recruiting
Phase N/A
Start date February 2016
Completion date December 2026

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