Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06202222

Interest of Intensive Postoperative Rehabilitation Following Minimally Invasive Lung Resection

Led by University Hospital, Rouen · Updated on 2025-09-10

184

Participants Needed

3

Research Sites

138 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

For patients diagnosed with non-small cell lung cancer (NSCLC), lung resection surgery remains the gold standard for curative treatment. This scheduled operation is associated with significant morbidity, particularly in individuals with impaired cardio-respiratory function. Therefore, patient optimization is paramount. The process begins prior to surgery with preoperative rehabilitation, commonly referred to as "prehabilitation," serving as the foundation for various Enhanced Recovery After Surgery programs. The training methods employed in these programs bear similarity to rehabilitation programs designed for patients with chronic obstructive pulmonary disease (COPD). Postoperatively, patients undergoing thoracic surgery partake in daily physiotherapy sessions, aiming to optimize the postoperative period, minimize the respiratory impact of surgery, and reduce the length of hospital stay. However, this treatment is not currently standardized and primarily involves early mobilization, including walking, and respiratory physiotherapy. Our focus is on the intensity and methods of this postoperative rehabilitation. There is limited literature on effective early rehabilitation in the immediate postoperative period, and existing studies suggest no adverse events associated with postoperative training. Therefore, our objective is to assess whether combining endurance training with standard physiotherapy (walking and respiratory physiotherapy) enhances the functional capacity of individuals undergoing lung surgery.

CONDITIONS

Official Title

Interest of Intensive Postoperative Rehabilitation Following Minimally Invasive Lung Resection

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients requiring surgery for diagnosed or undergoing diagnosis of lung cancer.
  • Patients in need of major lung resection through a minimally invasive approach.
  • Patients capable of performing the chair rise test.
Not Eligible

You will not qualify if you...

  • Contraindications to cyclo-ergometry, such as deep vein thrombosis in a lower limb.
  • Patients with one or both lower limbs amputated.
  • Rheumatological pathology, trauma, or previous surgery in the lower limb, pelvis, or spine causing limited joint movement or strict immobilization.
  • Severe dermatological conditions preventing prolonged sitting on a bicycle.
  • Glasgow score less than 15.
  • Patients who have not undergone pulmonary resection by minimally invasive surgery.
  • Patients hospitalized outside the thoracic surgery department before the first post-operative visit with the physiotherapist on Day 0.

AI-Screening

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Trial Site Locations

Total: 3 locations

1

Valenciennes, Hospital

Valenciennes, Hauts-de-France, France, 59322

Actively Recruiting

2

CAEN, university Hospital

Caen, Normandy, France, 14033

Actively Recruiting

3

Rouen, University Hospital

Rouen, Normandy, France, 76 031

Actively Recruiting

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Research Team

J

Jean-Marc BASTE, PhD

CONTACT

F

Fairuz BOUJIBAR, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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