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Distributed Registry Study
The purpose of this study is to test if a patient can be directly connected to a quality assurance (QA) database, traditionally known as a registry. Patient-reported outcomes (PRO) data will be entered into the database directly from a patient's mobile phone from their index procedure for 12 months. The investigators hope this study to be a "proof of concept" for such a distributed registry and evaluate 1) consistency of data acquisition, 2) engagement of patients, 3) overall value of patient-reported outcomes to enhance long term follow up.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
Yes
Palo Alto Veterans Hospital
Palo Alto, California, United States
Stanford
Palo Alto, California, United States
Start Date
April 1, 2019
Primary Completion Date
September 30, 2019
Completion Date
March 1, 2021
Last Updated
May 10, 2023
100
ACTUAL participants
Patient reported outcomes
BEHAVIORAL
Lead Sponsor
Stanford University
Collaborators
NCT07472049
NCT07161583
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.
View ClinicalTrials.gov Terms and ConditionsNCT07322913