Monitoring COPD Exacerbations Without Contact

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to identify early signs of COPD exacerbations before patients recognize symptoms. Participants will use a device called DistaSense placed on their mattress to monitor biological signals during sleep, while also completing a daily COPD Assessment Test (CAT). The study seeks to determine which biological indicators are most effective in predicting exacerbations and how these compare to daily symptom assessments.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Confirmed diagnosis of COPD
2. 1 or more exacerbation in the last year
3. Aged over 18 years
4. Willing to use monitoring devices and complete study questionnaires
5. Adequate English
6. Signed consent form

Exclusion Criteria:

1. Pregnancy
2. BMI greater than 45 kg/m2
3. Nil other, provided inclusion criteria are met.

Where it's running

• Royal Free Hospital
  London, United Kingdom Recruiting

Study contacts

• Principal investigator: John Hurst — University College, London
• Study coordinator: Eric Howie
• Email: ehowie@distasense.com
• Phone: 4084213151

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.