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The Use of Entropy to Assess Sleep Disordered Breathing in Chronic Respiratory Disease

Sponsor: University College, London

NCT ID: NCT07060079

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Not specified by the sponsor
How long the study runs
Study runs about 17 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
120
Started
2025-04-30
Last checked
2025-07

Plain English Summary

What is this study?

  • • Testing a new treatment for bronchial asthma
  • • Clinical study - 120 participants
  • • Research is being conducted into chronic respiratory diseases, including chronic obstructive pulmonary disease (COPD), asthma, interstitial lung disease, and bronchiectasis

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with bronchial asthma

Where?

  • • London - Royal Free hospital

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

Research is being conducted into chronic respiratory diseases, including chronic obstructive pulmonary disease (COPD), asthma, interstitial lung disease, and bronchiectasis. The investigation specifically focuses on sleep-disordered breathing (SDB) in individuals with chronic respiratory disease. SDB encompasses a range of conditions, the most common of which is obstructive sleep apnoea. In obstructive sleep apnoea, periodic pauses in breathing (apnoea) lead to reduced blood oxygen levels. To detect these events, patients typically undergo sleep studies that involve monitoring oxygen saturation, heart rate, and respiratory patterns during sleep. When chronic respiratory disease and SDB coexist, breathing disturbances during sleep may be exacerbated. To identify SDB, sleep studies are commonly used to assess oxygen levels, heart rate, and breathing patterns. The objective of this research is to identify differences between patients with chronic respiratory diseases who have SDB and those who do not. This will be achieved by analysing sleep study data using a novel analytical approach. The aim is to determine whether this method can yield more detailed insights into the underlying pathophysiology of these conditions.

More detail

Sleep is a complex and dynamic interplay between the brain and various physiological systems. Functions such as heart rate, respiration, and brain wave activity are regulated by intricate physiological mechanisms involving nonlinear interactions across multiple control centres operating on different time scales. It is increasingly recognized that a more accurate understanding of physiological outputs can be achieved through nonlinear analytical approaches, rather than traditional linear methods such as the standard deviation of the mean. Among nonlinear techniques, entropy is one of the most widely used metrics for assessing the irregularity of physiological signals. For example, sample entropy is a method used to quantify regularity in time series data and has demonstrated the ability to distinguish between healthy and diseased individuals. In some cases, recordings from a simple finger pulse oximeter (measuring oxygen saturation (SpO₂)) may be sufficient to screen for sleep apnoea, potentially reducing the need for full cardiorespiratory polygraphy. While nonlinear methods are well established in cardiovascular research, their application to respiratory signal analysis in obstructive sleep apnoea (OSA) remains limited. This analytical approach may offer deeper insights into complex physiological interactions-such as those between oxygen saturation and heart rate using relatively simple equipment. The aim of this study is to investigate differences in entropy values between healthy individuals and patients with chronic respiratory diseases, both with and without coexisting sleep-disordered breathing.

Bronchial AsthmaBronchiectasisILDCOPDOSAHSOSAObesity Hypoventilation Syndrome (OHS)

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What we know so far

Condition· Matched your search
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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

Biomarkers mentioned

previously negative

What the study is looking for

  • ✓All adult patients (≥ 18years) with chronic respiratory disease with/without SDB.
  • ✓patients who have had previously negative studies as a control group.
  • ✓Subject is able to read, understand, and sign the agreement to take part form.
  • ✓Willing to sleep with portable monitoring devices.

Who cannot take part

  • ✗Patients who are under 18 years of age at the time of the index study.
  • ✗Contraindications to the use of portable monitoring.
  • ✗Inability to give agreement to take part to take part in the study.
See the full criteria
Inclusion Criteria: * All adult patients (≥ 18years) with chronic respiratory disease with/without SDB. * patients who have had previously negative studies as a control group. * Subject is able to read, understand, and sign the informed consent form. * Willing to sleep with portable monitoring devices. Exclusion Criteria: * Patients who are under 18 years of age at the time of the index study. * Contraindications to the use of portable monitoring. * Inability to give informed consent to take part in the study.

Where Is This Study? (1 UK site)

Royal Free hospital

London NW3 2QG, United Kingdom

Recruiting
Site contact (verified)
Nawal Alotaibi, Phd student02080168375n.alotaibi@ucl.ac.uk

How to Get in Touch

Nawal Alotaibi

Sponsor contact

CONTACT

02080168375 n.alotaibi@ucl.ac.uk
Data sourced from ClinicalTrials.gov · Last verified: 2025-07