Multicenter pilot study to determine the feasibility of a multimodal prehabilitation program in patients with non-small cell lung cancer undergoing anatomical lung resectio
- Conditions
- 10029107Non-small cell lung carcinomalung cancer10038666
- Registration Number
- NL-OMON48205
- Lead Sponsor
- Maxima Medisch Centrum
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
- *18 years of age
- NSCLC, pathologically confirmed or high clinical suspicion
- Eligible for anatomical lung resection, that will be performed in MMC or ASz
- Straight forward preoperative work-up, with confirmation of eligibility for
surgery by lung surgeon before the multidisciplinary team meeting
- Written informed consent
- Inability to give written informed consent (illiteracy, language barrier,
cognitive disabilities)
- Contra-indication for training (e.g. comorbid conditions, signs of
undiagnosed cardiac disease, physical or psychological impairments)
- Renal insufficiency, defined as estimated Glomerular Filtration Rate (eGFR)
<60 ml/min/1.73m2 (estimated using the Modification of Diet in Renal Disease
(MDRD) formula in the MMC and estimated using the Chronic Kidney Disease
Epidemiology Collaboration (CKD-EPI) formula in the ASz)
- Participation in MEDIAST trial (NTR6528; NL60692.015.17)
- In case of patients in ASz: referral by pulmonologist from Beatrix hospital,
Gorinchem (the Netherlands) for surgery in ASz
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method