Actively Recruiting

Age: 18Years - 90Years
All Genders
Healthy Volunteers
ID07615504

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

Age: 18Years - 90Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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)

Long-term Monitoring

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

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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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