Viewing Study NCT02326532


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Study NCT ID: NCT02326532
Status: UNKNOWN
Last Update Posted: 2020-09-09
First Post: 2014-12-09
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Incorporation of Patient Reported Outcomes Data in the Care of US Veterans With Rheumatoid Arthritis
Sponsor: North Florida Foundation for Research and Education
Organization:

Study Overview

Official Title: Incorporation of Patient Reported Outcomes Data in the Care of US Veterans With Rheumatoid Arthritis
Status: UNKNOWN
Status Verified Date: 2020-09
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PRO
Brief 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.
Detailed 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 Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: