Effects of Preoperative Rehabilitation in Patients Resected for Lung Cancer
NCT ID: NCT03020251
Last Updated: 2025-12-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ACTIVE_NOT_RECRUITING
NA
90 participants
INTERVENTIONAL
2017-05-12
2026-02-28
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
NONE
Study Groups
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control group (C group)
patient will receive preoperative chest physiotherapy (standard supportive care)
preoperative chest physiotherapy
preoperative chest physiotherapy : 5 sessions per week during 3 weeks
rehabilitation group (R group)
patient will receive preoperative chest physiotherapy and a preoperative rehabilitation program at home (exercise training)
preoperative chest physiotherapy
preoperative chest physiotherapy : 5 sessions per week during 3 weeks
preoperative rehabilitation program
exercise training at home : 5 sessions per week during 3 weeks
Interventions
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preoperative chest physiotherapy
preoperative chest physiotherapy : 5 sessions per week during 3 weeks
preoperative rehabilitation program
exercise training at home : 5 sessions per week during 3 weeks
Eligibility Criteria
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Inclusion Criteria
* Age \> 18 years
* Presence of Chronic Obstructive Pulmonary Disease (COPD) stages 2-4 of Gold (forced expiratory volume (FEV )/ forced vital capacity (FVC) \<70%, FEV \<80% of predicted) and Exertional dyspnea stage MMRC (Medical Research Council) \> 1
* Patients must provide written consent
* Member of social security scheme
Exclusion Criteria
* COPD stage 1 Gold (VEMS \>= 80% of the theoretical value)
* Presenting an operating contraindication during the initial maximal exercise test
* Presenting cardiac or vascular contraindication to achieve the readaptation program
* Patient living alone at home
* Patient with ventilatory assistance at home (oxygen therapy or noninvasive ventilation (NIV))
* With exercise hypoventilation (PaCO2 \>45 mmHg)
* Cognitive difficulty
* unable major
* pregnancy,
* patients deprived of liberty by a court or administrative decision
18 Years
ALL
No
Sponsors
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Centre Jean Perrin
OTHER
Responsible Party
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Principal Investigators
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Marc FILAIRE, Pr
Role: PRINCIPAL_INVESTIGATOR
Centre Jean Perrin
Locations
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CHU Clermont Ferrand, Gabriel Montpied, service de médecine du sport et explorations fonctionnelles,
Clermont-Ferrand, , France
Centre de Recherche en Nutrition Humaine
Clermont-Ferrand, , France
Centre Jean Perrin
Clermont-Ferrand, , France
CHU Grenoble, Hôpital Michallon
Grenoble, , France
Hospices Civiles de Lyon, groupement hospitalier Est, Hopital Louis Pradel
Lyon, , France
CHU Saint-Etienne, CHU Hopital Nord
Saint-Etienne, , France
Countries
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References
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Laurent H, Galvaing G, Thivat E, Coudeyre E, Aubreton S, Richard R, Kwiatkowski F, Costes F, Filaire M. Effect of an intensive 3-week preoperative home rehabilitation programme in patients with chronic obstructive pulmonary disease eligible for lung cancer surgery: a multicentre randomised controlled trial. BMJ Open. 2017 Nov 12;7(11):e017307. doi: 10.1136/bmjopen-2017-017307.
Other Identifiers
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2016-A00622-49
Identifier Type: -
Identifier Source: org_study_id