Your voice could hold the key to spotting lung disease
NCT ID NCT04754490
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This study investigates whether patterns in speech and breathing can indicate the presence of obstructive respiratory diseases like COPD. Researchers will collect short voice recordings from patients with and without lung disease and compare them to standard lung function tests. The goal is to build a database of speech patterns that could one day lead to a simple, non-invasive diagnostic tool.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could lead to a simple, non-invasive way to screen for or monitor chronic respiratory diseases using just a voice recording.
- What could go wrong
- This is a small, early-stage study focused on collecting data, not testing a treatment. The approach may not prove accurate enough for real-world diagnosis.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
80 people
The number who actually took part.
- Started
-
Mar 2019
- Finished
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Jun 2026
- Lead sponsor
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A government agency
The lead sponsor is a government body.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patient \>18 years old referred for spirometry in the Respiratory Physiology Clinic at Prince Charles Hospital; Eligibility Criteria - Control Participants Control participants will be contact through the British Lung Foundations local groups who have indicated their willingness to be involved in local clinical research to act as control participants. As all prospective participants will have had their respiratory function measured before taking part by a Respiratory Physiologist, we do not expect to have to screen for medical issues for participation in the study. Furthermore, the actual tests the participants will be undertaking will be non - invasive, submaximal and will require little or no effort.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
6.1.2 Inclusion criteria Patient Participants 1. Adult patient \>18 years old referred for spirometry in the Respiratory Physiology Clinic at Prince Charles Hospital; 2. Clinically defined obstructive or restrictive respiratory disease (indicated by spirometry) 3. Clinically stable (indicated by being able to undergo spirometry) 4. No significant unstable disease co-morbidities (indicated by being able to undergo spirometry) 5. Capable of providing informed consent. 6. Willing to take part in all study measurements. 7. The speaking exercise will be conducted in English on this study. 8. Participants are not taking part in any other research. 6.1.3 Inclusion criteria Control Participants 1\. No obstructive or restrictive respiratory disease (indicated by spirometry) 2. Clinically stable (indicated by being able to undergo spirometry) 3. No significant unstable disease co-morbidity's (indicated by being able to undergo spirometry) 4. Capable of providing informed consent. 5. Willing to take part in all study measurements. 6. The speaking exercise will be conducted in English on this study. 7. Participants are not taking part in any other research. 6.1.4 Exclusion criteria for both Patient and Control Participants 1. Any form of challenge testing in the Respiratory Physiology Department involving salbutamol. 2. Severe Sensory and/or Cognitive Impairment 3. Inability to complete study measurements
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Cwm Taf Morgannwg Health Board
Abercynon, Wales, CF45 4SN, United Kingdom
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Other studies related to the condition(s) this trial covers.
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