Impact of Chronic Cough on Activities of Daily Living and Response to Acute High-intensity Exercise
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Chronic Cough (CC). Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United Kingdom
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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).
Primary outcome measures
- Physical activity status assessed using objective wearable accelerometer (ActiGraph LEAP) [Time frame: 1-week]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Case-control
Study locations
United Kingdom · 1 center
- University of Leeds — Leeds
Identifiers
NCT: NCT06766175 · 344527