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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02328430
Other study ID # 3480
Secondary ID
Status Not yet recruiting
Phase N/A
First received December 19, 2014
Last updated December 30, 2014
Start date January 2015
Est. completion date August 2015

Study information

Verified date December 2014
Source North Bristol NHS Trust
Contact James W Dodd, MB CHB PhD
Phone 01174147925
Email james.dodd@bris.ac.uk
Is FDA regulated No
Health authority United Kingdom: National Health Service
Study type Observational

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date August 2015
Est. primary completion date August 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility 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 -

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Device:
Kinnect 3 camera
comparison of Kinnect 3 measures of chest wall movement during standard spirometry

Locations

Country Name City State
United Kingdom North Bristol NHS Trust Bristol Avon

Sponsors (2)

Lead Sponsor Collaborator
North Bristol NHS Trust University of Bristol

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation between change in chest wall depth and Forced Expiratory Volume in 1 second (FEV1) Change in lung volume over time (litre per minute) participants will be followed up for the duration of outpatient visit - on average 3 hours No
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