Pulmonary Rehabilitation (PR)
Other20 sessions of PR in respiratory rehabilitation centre will be performed over a period of 3 months
NCT Number: NCT05015153
Pulmonary Embolism (PE) is a common and serious disease. Indeed, the annual incidence is 1/1000 patients per year and the 3-month mortality is 10%, which is twice that of myocardial infarction. The treatment is based on anticoagulation for at least 3 months. However, after three or six months of anticoagulation, persistent dyspnea and impairment of quality of life are observed in at least 30% of cases. Several mechanisms explain dyspnea and impairment of quality of life after PE, such as residual pulmonary artery obstruction, exercise deconditioning, depressive syndrome or development of a cardio-respiratory pathology. Pulmonary rehabilitation (PR) has been shown to be effective on dyspnea and quality of life and is included in the therapeutic management of chronic respiratory diseases such as Chronic Obstructive Pulmonary Disease (COPD) or pulmonary fibrosis. Furthermore, PR is also used after a myocardial infarction. However, PR after PE is still not included in therapeutic management of PE while outpatient management is recommended for the majority of patients after an acute PE episode. Study hypothesis is that PR has the potential to improve quality of life and dyspnea perception in patients who have received anticoagulation for at least 3 months after PE and who present an impairment of quality of life and/or a persistent dyspnea. This study presents several innovative aspects. First, to our knowledge, This study is the first large randomized trial assessing PR at least 3 months after acute symptomatic PE. Only one small randomized trial on 18 patients evaluating the impact of PR after PE has been published; as PR was performed just after the acute phase of PE in this trial, the clinical status improvement observed in this study could not be explained by PR alone, but also by anticoagulation. In this study, the investigators will include 112 patients at least 3 months after PE in order to exclude the bias related to anticoagulation effect. Second, This study is the first large randomized trial. Third, this study is the first that have the potential to demonstrate efficacy and safety of delayed PR after PE in patients with impaired quality of life due to persistent residual dyspnea.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
CHU Brest, Brest, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
20 sessions of PR in respiratory rehabilitation centre will be performed over a period of 3 months
Time frame: 3 months
Pulmonary embolism Quality of life score. This score includes 6 items regarding the frequency of lung complaints, their intensity, their physical, personal, social and professional impact. For each item, an average score is collected
Time frame: 3 months
Number of events
Time frame: 15 months
Pulmonary embolism Quality of life score. This score includes 6 items regarding the frequency of lung complaints, their intensity, their physical, personal, social and professional impact. For each item, an average score is collected
Time frame: 3 months
Pulmonary Vascular Obstruction (Meyer score) assessed with V/Q lung scan
Time frame: 3 months and 15 months
Multidimensional dyspnea Profile (MDP) at the cycloergometer, Borg scale at the cycloergometer and at the 6 minute-walk-test, and Modified Medical Research Council scale (MMRC)
Time frame: 3 months and 15 months
6 Minutes Walk Test
Time frame: 3 months and 15 months
Score of Hospital Anxiety and Depression scale. 14 rated items from 0 to 3. Seven questions relate to anxiety (total A) and seven others to the depressive dimension (total D), allowing thus obtaining two scores (maximum score for each score = 21)
Time frame: 15 months
Number of events
Time frame: 15 months
Number of events
Time frame: 15 months
Number of events
Time frame: 15 months
Number of events
Contact information is provided by the study sponsor or research team.
University Hospital, Brest
Other
Acronym: RAMBO
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.
Published trials that share one or more normalized conditions with this study.
NCT05103670
Cardiovascular Diseases, Dyspnea
Brest, France
View Trial DetailsNCT04615065
Acute Disease, Acute Kidney Injury
Groningen, Netherlands
View Trial DetailsNCT04920695
Cardiovascular Diseases, Dyspnea
Kingston, Ontario, Canada
View Trial DetailsNCT00707811
Asthma, Bronchial Diseases
Cleveland, Ohio, United States
View Trial Details