Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07460999

Effects and Mechanisms of Online Delivered Singing Training vs Usual Care in Patients With Persistent Symptoms 6-18 Months After Surgical Resection for Non-small Cell Lung Cancer (NSCLC) - a Multi-centre RCT

Led by Zealand University Hospital · Updated on 2026-04-02

100

Participants Needed

5

Research Sites

26 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating whether an online singing training program can improve physical function, reduce symptoms, and enhance quality of life in people who have undergone surgery for non-small cell lung cancer (NSCLC) six to eighteen months earlier. This study compares singing training to usual care in a multi-center randomized controlled trial. Singing has shown benefits in respiratory diseases like COPD, which shares symptoms with NSCLC, and this study aims to see if similar benefits apply to lung cancer patients. Participants will be randomly assigned to either a 10-week online singing training program based on the Singing for Lung Health (SLH) approach or to usual care followed by singing training after the initial period. The singing sessions are held twice a week for 1.5 hours, delivered by trained singing teachers, and include physical warm-ups, vocal exercises, singing, movement, and playful activities. Participants may also continue other physical or singing activities during the study. During the trial, participants will be assessed before and after the 10-week intervention period using measures such as the Six Minute Walking Test, perceived exertion, quality of life questionnaires, and symptom burden evaluations. Researchers will monitor changes in physical capacity, breathlessness, anxiety, depression, and other health-related outcomes. Adherence and any adverse events will be recorded. The study is expected to run from early 2026 to late 2027, with multiple follow-up assessments for participants.

CONDITIONS

Brief Title

Singing Training vs Usual Care 6-18 Months After Surgical Resection for Non-small Cell Lung Cancer (NSCLC)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Persistent symptoms 6-18 months after surgical resection of localized lung cancer using video-assisted thoracoscopy (VATS)
  • Stage I lung cancer surgery performed 6-18 months earlier
  • Motivated to participate and accept randomization
  • Access to a computer or tablet with internet
  • Ability to speak and understand Danish
  • Willing to attend singing sessions twice a week as scheduled
Not Eligible

You will not qualify if you...

  • Unstable coronary diseases
  • Severe cognitive disabilities such as dementia
  • Need for adjuvant chemotherapy or other cancer treatments
  • Signs of lung cancer recurrence on follow-up CT scans

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) for screening and enrollment

Treatment

Duration - 10 weeks

Participants receive 10 weeks of online singing training according to the Singing for Lung Health (SLH) approach or usual care without additional intervention. Singing sessions include physical, vocal, and breathing exercises twice a week, lasting 1.5 hours each.

Twice weekly online sessions for 10 weeks

Follow-up

Duration - Up to 14 weeks after baseline

Participants are assessed for changes in physical capacity, quality of life, symptom burden, and other health outcomes after the treatment phase. Those initially receiving usual care are offered the singing training and followed again.

1 to 2 follow-up visits depending on group assignment

Trial Site Locations

Total: 5 locations

1

August Krogh Section for Molecular and Human Physiology, Department of Nutrition, Exercise, and Sports, Faculty of Health and Medical Sciences, University of Copenhagen

Copenhagen, Denmark, 2100

Actively Recruiting

2

Department of Respiratory Medicine, Bispebjerg Hospital

Copenhagen, Denmark, 2400

Actively Recruiting

3

Department of Medicine Roskilde and Næstved, Zealand University Hospital

Næstved, Denmark, 4700

Actively Recruiting

4

Department of Respiratory Medicine, Odense University Hospital

Odense, Denmark, 5000

Actively Recruiting

5

Department of Respiratory Medicine, Lillebaelt Hospital

Vejle, Denmark, 7100

Actively Recruiting

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Research Team

M

Mette Kaasgaard, PhD

U

Uffe Bødtger, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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