Interest of Intensive Postoperative Rehabilitation Following Minimally Invasive Lung Resection: A Randomized Controlled Study

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
Other Locations
France
CAEN, university Hospital
RECRUITING
Caen
Rouen, University Hospital
RECRUITING
Rouen
Valenciennes, Hospital
RECRUITING
Valenciennes
Contact Information
Primary
Jean-Marc BASTE, PhD
jean-marc.baste@chu-rouen.fr
+33 2 32 88 87 04
Backup
Fairuz BOUJIBAR, PhD
fairuz.biujibar@chu-rouen.fr
+33 2 32 88 89 90
Time Frame
Start Date: 2024-09-09
Estimated Completion Date: 2027-05-09
Participants
Target number of participants: 184
Treatments
No_intervention: standard rehabilitation
Experimental: standard rehabilitation and cycloergometer
Sponsors
Leads: University Hospital, Rouen

This content was sourced from clinicaltrials.gov