Understanding the Feasibility of a Co-designed Pre-radiotherapy Exercise Programme - A Single-arm Study

Recruiting now · Not applicable

Conditions studied: Lung Cancer

In brief

The goal of this clinical trial is to understand the feasibility of a co-designed, pre-radiotherapy exercise programme for people with stage I-III non-small cell lung cancer. This involves people with lung cancer engaging in 20 minutes exercises sessions performed within the radiotherapy department and immediately before each treatment at a personalised intensity. The main questions it aims to answer are: To understand the acceptability of the exercise programme through monitoring recruitment rates, attendance of the exercise sessions, and adherence to prescribed exercise intensities. Adverse events will also be monitored to understand programme safety. Follow-up qualitative interviews will be conducted with participants, their family members, and health care professionals (HCP) to further explore the acceptability of the exercise programme. In total, participants will be invited to perform twenty, supervised exercise sessions scheduled immediately before each treatment within the radiotherapy department. Each exercise session will be twenty minutes in duration and will be performed on a stationary exercise bike. Regarding exercise intensity, there are four levels which may be prescribed depending on people's exercise history, baseline exercise experience, and personal preference. Participants may progress or regress exercise intensity levels throughout the programme depending on their adherence and preference.

Key facts

Study ID

NCT07554677

Run by

Queen's University, Belfast

People needed

30

Starts

2026-06-10

Expected to finish

2026-12-01

Last updated by the study team

2026-06-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with clinically or histologically confirmed NSCLC stages 1-3.
• Planned to receive treatment with curative intention radiation as primary treatment.
• Eastern Cooperative Oncology Group (ECOG) performance status 0-2.
• At least 18 years of age.
• Can understand and communicate in English.
• Deemed safe to participate in moderate-intensity exercise and for ECG monitored maximal fitness test through the completion of a medical clearance form by their treating physician.
• Able to provide written and informed consent.

You may not qualify if…

• Unstable or new angina (diagnosed within the previous month).
• Unstable or acute heart failure, cardiomyopathy, or other uncontrolled cardiac disease (as evidenced by symptomatic fluid retention, excessive breathlessness, rapid weight gain, swollen ankles or pitting oedema) within the previous 3 months.
• Presence of new or uncontrolled cardiac arrhythmias.
• Confirmed or suspected spinal cord compression.
• Uncontrolled diabetes (e.g. medication changed within 1 month, has had episodes of hypoglycaemia during the previous 2 weeks, or hyperglycaemia which does not decrease with exercise during the previous 2 weeks).
• Is receiving combination treatment with chemotherapy or immunotherapy.
• Current active secondary malignancy other than non-melanoma skin cancer.
• Has had orthopaedic surgery within the previous 3 months on weight-bearing bones.
• Chest pain while undertaking exercise or physical activity.
• No > Grade 2 peripheral neuropathy.
• Metastatic disease beyond localised metastatic involvement (e.g. bone or brain).
• Has discovered any abnormalities shown on the ECG monitored maximal fitness test which warrant early termination or contraindicate physical activity.
• People with living with a physical disability which would limit their ability to exercise safely on the stationary exercise bike used within this study.
• People who are non-English speakers.
• People who are pregnant.
• Patient participation in other clinical research - As an additional consideration, patients will be excluded if they are currently enrolled in an alternative exercise or physical activity study, as this may impact outcomes in both studies. However, if they have been involved in research prior to this or are currently involved in research in an unrelated area we will not immediately exclude them from trial participation. Instead, the Doctor of Philosophy (PhD) candidate, Chief investigator, and Principal investigator will discuss their involvement to determine safe and appropriate enrolment.
• Physical disability - it is with regret that we will be limited in our capacity to offer alternative exercises to accommodate people with a physical disability. To elaborate, the Belfast City Hospitals (BCH) main gym is willing to lend a stationary exercise bike to the research team in support of this study. However, due to limitations on equipment availability in the trust, and limited funding/resources to purchase equipment, people who have a physical disability which limits their capacity to exercise safely on the stationary bike will be excluded from this study. In an ideal scenario, we would also have a recumbent stationary bike to support more people with physical disability get involved within this research.

Where it is running

• Northern Ireland Cancer Centre, City Hospital, BHSCT — Belfast, Antrim, United Kingdom (enrolling)

Full record on ClinicalTrials.gov

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