Cost of Care for Juvenile Idiopathic Arthritis

Status Completed

Clinical Trial Summary

This project seeks to collect data on healthcare utilization and expenditure rates in Juvenile Idiopathic Arthritis (JIA) patients from across the US, correlate these costs with disease activity and outcome measures and determine methods by which to reduce the economic impact while improving outcomes.

Clinical Trial Description

SPECIFIC AIMS AND OBJECTIVES

The specific aims of this registry protocol are:

- To create and maintain a secure online database of patients with JIA

- To collect data elements related to cost of care in patients with JIA

- Compare standard outcome and disease activity measures to health care expenditures in JIA

- To determine methods by which to reduce costs while improving outcomes and quality of care

The study plans to enroll 300 or more subjects from 3 medical centers in the US over a 24 month period. Subjects in the study are patients with Juvenile Idiopathic Arthritis.

Enrollment into the protocol will include key demographic and clinical data including, medication exposures, disease severity, and function including disease-specific data elements; and estimates of health care service utilization and health care expenditures. Data will be collected once per subject within the context of a standard of care visit. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01469897
Study type	Observational
Source	The Cleveland Clinic
Contact
Status	Completed
Phase	N/A
Start date	January 2012
Completion date	March 2017

View Details

See also
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