Lung Cancer 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:
- You are 18 years old or older
- You can speak, read, and understand English
- You identify as non-Hispanic Black or non-Hispanic White
- You were diagnosed with invasive lung cancer (that has not spread to other parts of the body) within the last 24 months, confirmed by a tissue test
- You have had surgery for your lung cancer (mainly for stage I, II, or III) and have finished all cancer treatments, including surgery, chemotherapy, and radiation
- You are willing to give a blood sample, which would be collected at your home by a visiting blood draw service
- You are willing to sign a consent form showing you understand the nature of the study before taking part
Who may not be able to join:
- Your cancer was diagnosed as stage 0 (very early, non-invasive) or stage IV (has spread to other parts of the body)
- You have certain health conditions that make breathing muscle exercises unsafe for you, such as a recent blood clot in the lungs, an aortic aneurysm, or a current collapsed lung (confirm with trial site)
- You are already regularly following a structured exercise program or currently meeting general exercise guidelines
- You are unwilling or unable to follow the study's requirements
- The trial doctor believes, for any reason, that you are not a suitable candidate for the study
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.
GP referral letter
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Trial details
Where this trial is recruiting
Primary endpoints
Percentage of patients who complete at least 3 respiratory muscle training (RMT) sessions/week (Compliance) (Aim 1); Proportion of planned sessions completed (Adherence) (Aim 1); Proportion of total completed to total planned cumulative dose (Tolerability) (Aim 1); Inspiratory muscle strength (Aim 2); Change in dyspnea (Aim 2)-Dyspnea-12 survey; Change in dyspena (Aim 2)- Functional Assessment of Chronic Illness Therapy (FACIT) dyspnea; Change in cancer-related fatigue (Aim 2) - Brief Fatigue Inventory; Change in cancer related Fatigue (Aim 2) - FACIT fatigue scale; Circulating levels of myelo...
Can't join this trial?
Data last synced from ClinicalTrials.gov: 2 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.