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Assessing Health Related Quality of Life in Hypersensitivity Pneumonitis

Clinical Trial Details

Chronic Hypersensitivity Pneumonitis (CHP) is a chronic interstitial lung disease that occurs after longstanding or recurrent exposure to an inhaled stimulus. This disease affects many patients in our pulmonary practice. We know from prior research that living with CHP has an impact on patients’ quality of life. We have recently designed a survey that asks questions that specifically address how CHP impacts patients’ lives. The purpose of this study is to validate the newly developed survey so that it may be used in the future to assess patients’ quality of life both in clinical practice and in research trials.

The study will involve two separate “study visits”. We will schedule you for the first study visit with one of our research team members. In this session we will ask you to complete the newly developed quality of life survey for CHP, as well as two other quality of life surveys and a brief demographics/medical history form. We will also be collecting Pulmonary Function Test and 6 Minute Walk Test results along with other medical history and demographic information. The entire initial visit should take on average 1 hour of your time. The second study visit will be scheduled for two weeks (+/- 3 days) after the initial visit. The purpose of this visit will be to have you complete the newly developed CHP survey (only this survey at this time) a second time. This session should take no more than 30 minutes.

During the COVID-19 pandemic, all study components will occur virtually via telephone or Zoom, email, and REDCap. Relevant medical information including the most recent Pulmonary Function Test results and 6-Minute Walk Test results will be taken from patient medical charts.

Key Eligibility: 

Inclusion Criteria

  • 18 years old or older
  • Understand and sign the informed consent document
  • Documented diagnosis of HP made and confirmed at an ILD center via expert consensus or in multidisciplinary discussion. Diagnosis based upon a minimum of a medical history, physical examination, pulmonary function testing, and computerized tomography (CT) scan. Pathology will be reviewed if available but is not required.
  • HP must be the primary pulmonary disease
  • Anticipated ability to complete follow up survey within 2 weeks of initial survey completion

Exclusion Criteria

  • Non-English Speaking (Patient must be able to speak and read English fluently but it does not have to be their primary language)
  • Inability to complete questionnaire due to cognitive impairment

Study contact by location

Upper East Side - Manhattan

Contact(s)

Kerri Aronson, MD
(646) 962-2740
pulmonaryresearch@med.cornell.edu

Primary Investigator(s)

Protocol ID(s)

Weill Cornell Medicine IRB #:

1905020233

ClinicalTrials.gov:

NCT04273867

Status

Open to Enrollment

Age Group

Adult

Sponsor