Cough in Lung Cancer Cancer Malignant neoplasm of bronchus and lung
Conditions
Interventions
Day 0 Groups A and B: Case Report Form will be completed by investigator, Brief Reflux Inventory, Visual Analogue Scale (VAS), Manchester Cough in Lung Cancer Scale questionnaire and Quality of LIfe
Sponsors
The Christie NHS Foundation Trust (UK)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Histologically or cytologically confirmed Non Small Cell Lung Cancer (NSCLC) or Small Cell Lung Cancer (SCLC) 2. WHO performance 0-2 3. Ability to give informed consent to participate 4. Age =18 years
Exclusion criteria
Exclusion criteria: Patients unable to complete self-reporting questionnaires
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Frequency of cough, measured using 24-hour ambulatory cough monitoring at baseline and day 60 in a subset of patients 2. Severity of cough, measured using the Cough Severity Visual Analogue Scale at baseline, day 30 and day 60; the Cough Severity Diary at baseline and day 60; and the EORTC LC13 questionnaire at baseline and day 6060 and the Common Toxicity Criteria for Adverse Events v 4.0 at baseline and day 60 | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Impact of cough on quality of life measured using the Manchester Cough in Lung Cancer Scale at baseline, day 30 and day 60 2. Clinical factors associated with cough severity and cough impact scores at baseline and day 60 | — |
Countries
England, United Kingdom
Outcome results
None listed