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Clinical Trials/NCT02328430
NCT02328430UnknownNot Applicable

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

North Bristol NHS Trust1 site in 1 country100 target enrollmentStarted: January 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
100
Locations
1
Primary Endpoint
Correlation between change in chest wall depth and Forced Expiratory Volume in 1 second (FEV1)

Study Overview

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.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

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

Exclusion Criteria

  • •Unable to give informed consent
  • •Unable to perform spirometry -

Outcomes

Primary Outcomes

Correlation between change in chest wall depth and Forced Expiratory Volume in 1 second (FEV1)

Time Frame: participants will be followed up for the duration of outpatient visit - on average 3 hours

Change in lung volume over time (litre per minute)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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