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Impact of Chronic Cough on Activities of Daily Living and Response to Acute High-intensity Exercise

Recruiting
Conditions
Chronic Cough (CC)
Registration Number
NCT06766175
Lead Sponsor
University of Leeds
Brief Summary

Chronic cough is a common and debilitating condition that affects up to 10% of the global population. The health impact of chronic cough is multifaceted and manifests both physical and psychological symptoms including syncope, chest pain, lethargy, depression and anxiety. It is now also recognised that chronic cough often leads to social isolation and may impact an individual's ability or confidence to undertake routine daily tasks / lead an active lifestyle.

The primary aim of this study is therefore to characterise the impact of unexplained chronic cough on the ability to undertake daily activities - i.e., determine whether individuals with chronic cough exhibit impaired levels of physical activity during usual daily living when compared with healthy age, gender and BMI matched controls. A secondary aim is to assess the short-term impact of high-intensity exercise on cough (i.e., determine whether an acute bout of exercise alters cough frequency and/or severity).

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
129
Inclusion Criteria
  • Age >18 years
  • Chronic cough as per European Respiratory Society definition (>8 weeks duration)
  • High symptom burden (i.e., cough visual analogue scale >40 mm at pre-study screening)
  • Chest radiograph or CT within 3 years of the screening visit with no abnormalities considered to contribute to chronic cough
Exclusion Criteria
  • Smokers or individuals who gave up smoking within 12 months

  • Smoking history >20 pack-years

  • Long-COVID or post-COVID syndrome (defined as symptoms lasting over 12-weeks in duration)

  • Recent exacerbation of cough within 4 weeks of inclusion

  • Respiratory tract infection within 4 weeks of inclusion

  • Currently taking any of the following medications:

    • ACE inhibitors and within 3 months of inclusion
    • Antitussives (opioids, pregabalin, gabapentin, amitriptyline, nortriptyline, or over the-counter medications) within 2 weeks of inclusion
    • Medical treatments for gastro-oesophageal reflux disease (GORD), eosinophilic bronchitis or other cough related conditions, initiated or changed (i.e., not in a stable regimen) for 4 weeks prior to inclusion
  • Medical history of asthma or exercise-induced bronchoconstriction (EIB), COPD, or chronic bronchitis in the judgement of the investigator

  • Medical conditions/history or other circumstances which, in the judgement of the investigators, could increase the risk of adverse events or bias the study results

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Physical activity status assessed using objective wearable accelerometer (ActiGraph LEAP)1-week

Physical activity status including:

- Absolute daily steps

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Leeds

🇬🇧

Leeds, West Yorkshire, United Kingdom

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