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Clinical Trial Summary

The overall goal of this proposal is to address barriers to the use of patient reported outcome (PRO) data in the Dept. of Veterans Affairs (VA) health care system.


Clinical Trial Description

This is a randomized, controlled, single-blinded study that compares outcome data in patients for whom PRO data either is or is not made available to the treating physician. The question addressed by this proposal is whether patient reported outcome (PRO) data change patient's outcomes. The hypothesis is that the availability of these data in the form of the patient-completed Multidimensional Health Assessment Questionnaire/routine assessment of patient index data (MDHAQ/RAPID3) questionnaire will change patient-centric outcomes such as patient reported well-being, patient satisfaction and medication compliance. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02326532
Study type Interventional
Source North Florida Foundation for Research and Education
Contact
Status Active, not recruiting
Phase N/A
Start date February 2015
Completion date June 1, 2021

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