Actively Recruiting
Better Tests- Improving Diagnostic Accuracy and Prognostication in Interstitial Lung Diseases
Led by University of Dundee · Updated on 2026-05-29
750
Participants Needed
3
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Dundee
Lead Sponsor
B
British Pigeon Fanciers Medical Research
Collaborating Sponsor
AI-Summary
What this Trial Is About
This research aims to improve diagnosis and prediction of outcomes in people at risk for or diagnosed with interstitial lung diseases (ILD). It focuses on evaluating non-invasive tests based on blood and breath samples, especially among Pigeon Fanciers who have a higher risk of developing ILD due to their bird exposure. The study will also include patients diagnosed with ILD, including those with severe respiratory failure, to better understand how these tests relate to disease progression and patient experience. Participants will be grouped as active Pigeon Fanciers, ILD clinic patients, or hospital patients with ILD. Initial assessments for Pigeon Fanciers include collecting height, weight, lung function tests, medical history, and pigeon exposure details. Blood samples will be taken to measure antibodies and other biomarkers, and breath samples will be collected for analysis. Repeated assessments will be done over time to observe changes related to exposure or illness development. Participants will attend assessments at national pigeon meetings or clinical visits, where researchers will measure lung function, collect samples, and record symptoms and health changes. These data will help link test results to clinical outcomes over five years, including disease progression, treatment response, and survival. The study also evaluates how acceptable these tests are to participants, aiming to guide future clinical trials and improve ILD care.
CONDITIONS
Brief Title
Better Tests- Improving Diagnostic Accuracy and Prognostication in Interstitial Lung Diseases
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants must be active Pigeon Fanciers, attend ILD clinics, or be hospitalized with severe respiratory failure due to ILD
- Able to provide informed consent
- Adults aged 18 to 90 years
You will not qualify if you...
- Unable to provide informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo assessments including collection of height, weight, lung function tests, blood samples for antibody levels and storage, and breathing tests to analyze exhaled air. Health history and exposure information are also collected.
1 visit (in-person)
Duration - Up to 5 years
Participants return for follow-up assessments at large national meetings to repeat candidate tests and observe natural variation, exposure effects, and development of new medical conditions over time.
Multiple visits at national meetings over several years
Trial Site Locations
Total: 3 locations
1
Winter Gardens
Blackpool, United Kingdom, FY1 1HU
Actively Recruiting
2
Ninewells Hospital
Dundee, United Kingdom, DD21UB
Actively Recruiting
3
Perth Royal Infirmary
Perth, United Kingdom, PH1 1NX
Actively Recruiting
Research Team
M
Mark Spears, PhD FRCP
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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