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Feasibility and Validity of Remote Lung Function Assessment

Comparison of Remote Camera Measures of Lung Function Compared to Standard Spirometry

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02328430
Enrollment
100
Registered
2014-12-31
Start date
2015-01-31
Completion date
2015-08-31
Last updated
2014-12-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Lung Disease

Brief summary

Comparison of standard spirometry to non invasive remote lung function measures of chest wall movement using depth camera technology.

Detailed description

This study plans to test a new non invasive way of measuring lung function and compare it to the current method of blowing into a spirometer. Spirometry is an essential investigation for diagnosis and assessment of severity in people with Chronic Obstructive Pulmonary Disease (COPD) and other respiratory conditions, it is used in every respiratory unit and across primary care. It requires subjects to blow into a tube which measures volume and flow of expired air. It involves specialist equipment and training to perform and interpret. Not all patients are capable of performing spirometry, in particular children, frail, cognitively impaired and those experiencing a flare or exacerbation of symptoms. Remote lung function assessment technology has the potential to enable assessment of lung function in these groups of patients. In the future it is also hoped that it could be used to improve respiratory disease monitoring outside the healthcare environment such as in the patients home. This new method uses the latest infra-red depth detection cameras to measure chest wall movement. (N.B this does not capture identifiable images). We would like to record participants chest wall movements while blowing into the spirometer.

Interventions

DEVICEKinnect 3 camera

comparison of Kinnect 3 measures of chest wall movement during standard spirometry

Sponsors

University of Bristol
CollaboratorOTHER
North Bristol NHS Trust
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Patients attending outpatient department in respiratory medicine. 2. Scheduled to undergo spirometry -

Exclusion criteria

1. Unable to give informed consent 2. Unable to perform spirometry -

Design outcomes

Primary

MeasureTime frameDescription
Correlation between change in chest wall depth and Forced Expiratory Volume in 1 second (FEV1)participants will be followed up for the duration of outpatient visit - on average 3 hoursChange in lung volume over time (litre per minute)

Countries

United Kingdom

Contacts

Primary ContactJames W Dodd, MB CHB PhD
james.dodd@bris.ac.uk01174147925
Backup ContactDeborah Warbrick, BSc
deborah.warbrick@nbt.nhs.uk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026