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Assessing Health Related Quality of Life in Hypersensitivity Pneumonitis — CHP-HRQOL  

Interstitial Lung Disease Clinical Trial

Official title:
Assessing Health Related Quality of Life in Hypersensitivity Pneumonitis

Clinical Trial Summary

The objective of this study is to administer and validate a disease specific health related quality of life (HRQOL) survey for patients with Chronic Hypersensitivity Pneumonitis (CHP).

Clinical Trial Description

The objective of this study is to administer and validate a disease-specific health related quality of life (HRQOL) survey for patients with Chronic Hypersensitivity Pneumonitis (CHP). The survey items have been developed and revised from prior qualitative research with CHP patients. Potential participants will be recruited from WCMC, the Pulmonary Fibrosis Foundation (PFF) Registry and outside physician referral for the study. Participants will be asked to sign informed consent. At the initial visit participants will be asked to complete the survey and two additional PROs needed for concurrent validity testing. Participants will then be asked to complete the HRQOL survey under study a second time 2 weeks after the initial visit for test-re-test reliability testing. Pulmonary function testing and six minute walk test results will be collected. Pertinent demographic and clinical information will be collected from the patients and their medical records or registry data (if a PFF Registry participant). All information will be entered into a REDCap database for secure data management and storage. Psychometric testing will be performed on the overall survey instrument and the individual items in order to test validity and reliability. The goal is that the survey developed will be a reliable and valid measurement tool for use in both clinical practice and research settings. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04273867
Study type Observational
Source Weill Medical College of Cornell University
Contact
Status Completed
Phase
Start date July 10, 2020
Completion date February 22, 2023
View Details
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