Status:

UNKNOWN

Understanding Balance Impairment in COPD

Lead Sponsor:

Teesside University

Conditions:

Chronic Obstructive Pulmonary Disease

Healthy Volunteers

Eligibility:

All Genders

55+ years

Brief Summary

This study is an observational study investigating the mechanisms of balance problems in people with COPD and how COPD impacts them living their daily lives. The main objectives of this study are: *...

Detailed Description

Chronic obstructive pulmonary disease (COPD) is a progressive condition that affects around 1.2million people in the UK. Breathlessness is the main symptom but people with COPD are also more likely to...

Eligibility Criteria

Inclusion

  • COPD
  • Have a spirometry confirmed diagnosis of COPD as per GOLD guidelines
  • Stable COPD (six weeks clear of exacerbation)
  • 55 years or over at the point of recruitment
  • Able to communicate with good verbal English or use adaptive equipment to communicate
  • Male or female Controls
  • Free from a diagnosis of COPD (confirmed by spirometry)
  • 55 years or over at the point of recruitment
  • Able to communicate with good verbal English or use adaptive equipment to
  • Communicate
  • Male or female

Exclusion

  • COPD
  • Recent exacerbation of COPD (within the last six weeks)
  • Under 55 years of age at the point of recruitment
  • Any neurological or musculoskeletal diagnoses (e.g., strokes, Parkinson's disease or chronic pain that interferes with ability to safely complete the tests
  • Unable to provide written informed consent
  • Unable to speak English or no translation options available
  • Diagnosed but not corrected visual, vestibular disturbance and peripheral neuropathy
  • Vasovagal syncope
  • Not independent living (e.g., living in a care home or prison) Controls
  • Abnormal lung function (FEV1 and FVC equal to or greater than 80% and FEV1/FVC equal to greater than 70%)
  • Under 55 years of age at the point of recruitment
  • Any neurological or musculoskeletal impairment that would significantly affect balance impacting ability to safely complete the assessments
  • Unable to provide written informed consent
  • Unable to speak English or no translation options available
  • Any uncorrected visual or somatosensory disturbance
  • Vasovagal syncope
  • Living in a care home or in prison

Key Trial Info

Start Date :

July 17 2023

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

May 1 2024

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT05984498

Start Date

July 17 2023

End Date

May 1 2024

Last Update

August 9 2023

Active Locations (1)

Enter a location and click search to find clinical trials sorted by distance.

Page 1 of 1 (1 locations)

1

Teesside University

Middlesbrough, United Kingdom, TS1 3BX