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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.
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.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
Yes
Stanford School of Medicine
Stanford, California, United States
Start Date
February 1, 2016
Primary Completion Date
August 1, 2026
Completion Date
December 1, 2026
Last Updated
April 8, 2024
1,000
ESTIMATED participants
Randomized clinical study
OTHER
Lead Sponsor
Stanford University
NCT07469761
NCT06193083
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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