Viewing Study NCT02190916



Ignite Creation Date: 2024-05-06 @ 3:03 AM
Last Modification Date: 2024-10-26 @ 11:27 AM
Study NCT ID: NCT02190916
Status: COMPLETED
Last Update Posted: 2014-07-15
First Post: 2014-05-30

Brief Title: Vasculitis Illness Perception VIP Study
Sponsor: University of South Florida
Organization: University of South Florida

Study Overview

Official Title: Illness Perception Fatigue and Function in Systemic Vasculitis The VCRC Vasculitis Perception VIP Study
Status: COMPLETED
Status Verified Date: 2014-06
Last Known Status: None
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: None
Brief Summary: The purpose of this study is to learn about how patients with vasculitis think about their illness and to assess to what extent patient perceptions of illness are associated with physical mental and social functioning
Detailed Description: All patients enrolled in the Vasculitis Clinical Research Consortiums Contact Registry were invited via email to participate in this study The Contract Registry includes people who self-identify as having one of the following types of vasculitis granulomatosis with polyangiitis Wegeners microscopic polyangiitis Churg-Strauss syndrome polyarteritis nodosa Takayasus arteritis giant cell arteritis Behcets disease Henoch-Schöenlein purpura or CNS vasculitis People voluntarily enroll in this Registry with the understanding that they will receive information about clinical studies for which they might be eligible The introductory email included basic information about the study and all of the required elements for informed consent in a brief format Once participants agreed to participate in the study then they were directed to the online questionnaire

When completing the questionnaire patients were asked a series of questions Some of the follow-up questions depended on initial answers The questionnaire content was included as an appendix The online questionnaire version was thoroughly tested for usability

It was expected that most participants would require approximately 20-30 minutes to complete the questionnaire

The survey data is stored by the Rare Diseases Clinical Research Network Data Management and Coordinating Center DMCC at the University of South Florida The data is de-identified Names or other personal health information are not be collected

Study Oversight

Has Oversight DMC: None
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?: None