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NCT Number: NCT05636969

Multimodal Prehabilitation in Patients with Lung Cancer Undergoing Neoadjuvant Therapy

Neoadjuvant therapy (NAT) with chemoimmunotherapy is currently indicated for patients with locoregional advanced non-small cell lung cancer (NSCLC) prior to resection surgery, but literature has suggested that this is associated with decreased pulmonary function and potentially cardiorespiratory fitness, leading to increased risk of postoperative complications. In this study, we aimed to: 1) compare the effects of NAT on cardiorespiratory fitness (VO2peak) and lung function (DLCO, FEV1 and FVC) in patients with locoregional lung cancer undergoing prehabilitation before lung resection surgery.

Secondary objectives included:

1. To determine feasibility of the intervention (recruitment rate, competition rate and adherence) as well as safety (incidence of adverse events), particularly regarding the exercise component; 2. To quantify the effects of the intervention in terms of functional capacity (1min Sit-to-Stand Test), mood (Hospital Anxiety and Depression Scale) and self-reported physical activity (Yale Physical Activity Survey). 3. To assess the effects of multimodal prehabilitation on treatment completion (dose reductions/delays in planning/treatment withdrawal) as well as tolerability/toxicity (Coming Terminology Criteria for Adverse Events version 4.03) to chemo/immunotherapy 4. To assess the effects of multimodal prehabilitation on surgical outcomes (postoperative complications based on the Comprehensive Complication Index (CCI) of the Clavien-Dindo Classification System and length of hospital stay). 5. To determine the effect of the intervention on post-operative functional recovery by means of the 1-min Sit-To-Stand test conducted at hospital discharge.

In order to achieve this, we will conduct a prospective study including all patients with NSCLC scheduled for NAT (chemoimmunotherapy or chemotherapy alone) across four different hospitals in Spain and France. Patients will be identified from the multidisciplinary tumour board and will be subsequently referred to the oncologist consultation. After this, one of the members of the researchers will contact the patient and explain the purpose of the study. Those who are willing to participate, will be scheduled to undergo a CardioPulmonary Exercise Test (CPET) in addition to standard lung function tests (spirometry, diffusion capacity of carbon monoxide). After that, patients will be invited to participate in a multimodal prehabilitation program including supervised exercise training, home-based inspiratory muscle training, nutritional optimization and psychological support. Patients who refuse participation in the program due to logistic reasons, will be asked to serve as controls. In addition, we will also use data from a historical cohort including patients treated with chemoimmunotherapy prior to the implementation of the study as controls.

Patients will be assessed at baseline, after NAT and post-surgery (at hospital discharge).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hospital Clinic de Barcelona

Barcelona, 08036, Spain

Location status: Recruiting

Location contact

Raquel Sebio, PhD

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult patients with diagnosed non-small celll lung cancer (NSCLC) undergoing neoadjuvant therapy before lung resection surgery

Exclusion criteria

  • Physical impairments that prevent patients to perform a CardioPulmonary Exercise Test
  • Non-resectable tumours
  • Patients who refuse either surgical resection or neoadjuvant therapy

Treatment and study plan

Multimodal prehabilitation

Behavioral

The multimodal prehabilitation programme will consist of 1) twice weekly, supervised exercise training at the hospital gym for approximately 12-16 weeks; 2) nutritional consultation and diet optimization and supplementation if needed; 3) individual or group-based psychological support.

Primary outcomes

  1. Changes in cardiorespiratory fitness assessed with a cardiopulmonary exercise test

    Time frame: 2 weeks post-neoadjuvant therapy

    Differences in maximum oxygen consumption (VO2pic) pre to post neoadjvuant therapy during an incremental, symptom-limited test

Secondary outcomes

  1. Changes in diffusion capacity of carbon monoxide (DLCO)

    Time frame: 2 weeks post-neoadjuvant therapy

    Differences in diffusion capacity of carbon monoxide pre to post-neoadjuvant therapy

  2. Changes in submaximal cardiorespiratory fitness assessed with a cardiopulmonary exercise test

    Time frame: 2 weeks post-neoadjuvant therapy

    Differences in oxygen consumption at the anaerobic threshold (VO2AT) pre to post-neoadjuvant therapy during an incremental, symptom-limited test

  3. Changes in ventilatory efficiency (VE/VCO2 slope) assessed during a cardiopulmonary exercise test

    Time frame: 2 weeks post-neoadjuvant therapy

    Changes in ventilatory efficiency (VE/VCO2 slope) pre to post-neoadjuvant therapy

  4. Changes in pulmonary function (FEV1)

    Time frame: 2 weeks post-neoadjuvant therapy

    Differences observed in the maximum volume achieved during the first second (FEV1) of a forced spirometry test, pre to post-neoadjuvant therapy

  5. Changes in pulmonary function (FVC)

    Time frame: 2 weeks post-neoadjuvant therapy

    Differences observed in the forced ventilatory capacity (FVC) of a forced spirometry test, pre to post-neoadjuvant therapy

  6. Feasibility (recruitment rate ) of multimodal prehabilitation

    Time frame: 1 week before surgery

    Feasibility of the multimodal prehabilitation programme assessed by the recruitment rate (number of patients attending prehabilitation versus number of eligible patients)

  7. Feasibility (completion rate) of multimodal prehabilitation

    Time frame: 1 week before surgery

    Feasibility of the multimodal prehabilitation programme assessed by the completion rate (number of completers among those who accepted to participate in the programme)

  8. Adherence

    Time frame: 1 week before surgery

    Number of completed exercise sessions in the prehabilitation cohort versus number of scheduled sessions

  9. Adverse events

    Time frame: 1 week before surgery

    Number of adverse events registered during the exercise training sessions

  10. Postoperative Complications

    Time frame: within 30 days of hospital discharge

    Number and severity of postoperative complications will be assessed by reviewing medical records and calculating the Comprehensive Complication Index (CCI) according to the Clavien-Dindo Classification.

  11. 30-Day readmissions, re-interventions and emergency room visits

    Time frame: 30 days after surgery

    Readmissions, surgical re-interventions and emergency room visits post-discharge and during the first 30 days will be recorded by reviewing medical records

  12. Chemoimmunotherapy completion rates

    Time frame: 1 week post-neoadjuvant therapy

    Chemoimmunotherapy complete dosage, treatment delays and treatment withdrawal rates will be calculated and compared in both groups

  13. Post-surgery functional capacity

    Time frame: Same day as dicharge from hospital

    Functional capacity assessed with the 1 min Sit-to-Stand Test which consist of counting the number of times the patient can stand up and sit back onto a chair without arm support during one minute.

  14. Post-NAT functional capacity

    Time frame: 2 weeks post-neoadjuvant therapy

    Functional capacity assessed with the 1 min Sit-to-Stand Test which consist of counting the number of times the patient can stand up and sit back onto a chair without arm support during one minute.

  15. Post-NAT mood

    Time frame: 2 weeks post-neoadjuvant therapy

    Anxiety and depression symptoms will be assessed with a self-administer questionnaire, the Hospital Anxiety and Depression Scale

  16. Post-NAT self-reported physical activity

    Time frame: 2 weeks post-neoadjuvant therapy

    Self-reported physical activity levels will be measured using a validated questionnaire, the Yale Physical Activity Survey

Study contacts

Contact information is provided by the study sponsor or research team.

Graciela Martínez-Pallí, PhD

CONTACT

[email protected]

932275400

Raquel Sebio, PhD

CONTACT

[email protected]

+34634787194

Sponsors and collaborators

Lead sponsor

Hospital Clinic of Barcelona

Other

Collaborators

  • CHU de Rouen - Accueil
  • Consorci Hospitalari de Vic
  • Fundació Sanitaria de Mollet
  • Hospital General de Granollers

Registry information

Official study title

Effects of Multimodal Prehabilitation on Cardiorespiratory Fitness and Pulmonary Function During Neoadjuvant Therapy in Patients with Locally Advanced Lung Cancer

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Dec 5, 2022
Registry last updated
Mar 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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