NCT02328430

Brief Summary

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

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jan 2015

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 19, 2014

Completed
12 days until next milestone

First Posted

Study publicly available on registry

December 31, 2014

Completed
1 day until next milestone

Study Start

First participant enrolled

January 1, 2015

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2015

Completed
Last Updated

December 31, 2014

Status Verified

December 1, 2014

Enrollment Period

7 months

First QC Date

December 19, 2014

Last Update Submit

December 30, 2014

Conditions

Outcome Measures

Primary Outcomes (1)

  • 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

Interventions

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

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients attending UK secondary care outpatient department in respiratory medicine and how are scheduled to undergo spirometry

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

North Bristol NHS Trust

Bristol, Avon, BS10 5NB, United Kingdom

Location

Study Officials

  • James W Dodd, MB CHB PhD

    Academic Clinical Lecturer

    PRINCIPAL INVESTIGATOR

Central Study Contacts

James W Dodd, MB CHB PhD

CONTACT

Deborah Warbrick, BSc

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 19, 2014

First Posted

December 31, 2014

Study Start

January 1, 2015

Primary Completion

August 1, 2015

Study Completion

August 1, 2015

Last Updated

December 31, 2014

Record last verified: 2014-12

Locations