COPD Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have had surgery to remove early-stage (stage I) lung cancer using a keyhole surgical technique (called VATS), where the surgery took place between 6 and 18 months ago
- People who are still experiencing symptoms after their surgery, meaning at least one symptom has been rated as clinically significant on a standard quality-of-life questionnaire
- People who are willing to take part and comfortable with being randomly assigned to a group within the study
- People who have access to a computer or tablet with an internet connection
- People who can speak and understand Danish
- People who are able to attend singing sessions twice a week at the scheduled times
Who may not be able to join:
- People with unstable heart (coronary) disease
- People with severe cognitive difficulties, such as dementia
- People who have been recommended chemotherapy or other cancer-fighting treatments after their surgery
- People whose regular follow-up CT scan has shown signs that their lung cancer may have returned
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 4528940238
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in Physical capacity; Perceived exertion; Change in Health-related quality of life (HRQoL)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.