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Long-term Maintenance Benefits of a Pulmonary Rehabilitation Program Using a Mobile Digital Solution: a Prospective, Randomized, Controlled, Multicenter Study in a Population of COPD Patients (m-Rehab COPD)

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
telerehabilitation
Sponsored by
University Hospital, Montpellier
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring Chronic obstructive pulmonary disease, Telerehabilitation, Telemedicine, Exercise training, Quality of life, E-health, Connected objects, Care manager

Eligibility Criteria

40 Years - 78 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients diagnosed with COPD according to the GOLD (Global Initiative for Chronic Obstructive Lung Disease) creteria.
  • Presence of an incompletely reversible obstructive ventilatory disorder defined by a report VEMS / CVF lower than the lower limit of normal post-bronchodilator.
  • Patient on RR for four weeks in respiratory rehabilitation center.
  • Aged between 40 and 78 years.

Exclusion Criteria:

  • Presence of contraindications for exercise training (neuromuscular disease, orthopedic cause).
  • Patients with significant and unstable cardiovascular disease.
  • Inability to understand and/or answer questionnaires.
  • Refusal to use a smartphone or digital device.
  • Unable to access an internet connection at home.

Sites / Locations

  • Centre hopsitalier universitaire de Montpellier
  • Clinique du SouffleRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Telerehabilitation

Standard chronic care

Arm Description

Experimental group of 100 patients using the M-Réhab BPCO telerehabilitation solution. The solution will be provided during the fourth and final week of RR's stay during which patients will be trained to use all of the solution's features. Patients will carry out the entire post-rehabilitation using the remote rehabilitation solution and will benefit from medical assessments by teleconsultation at 1, 3, 6 and 12 months as well as assessments at 3, 6 and 12 months by filling. electronic auto-questionnaires followed by a telephone quality control if necessary. A final evaluation at 12 months, by videoconference, will be carried out at the patient's home.

following usual standard chronic care. Patients will receive during the last week of stay in the center, the usual advice to continue physical activity and nutritional advice at home. The evaluations at 3, 6 and 12 months will be done by electronic filling of auto-questionnaires followed by a telephone quality control if necessary. A final evaluation at 12 months, by videoconference, will be carried out at the patient's home.

Outcomes

Primary Outcome Measures

Quality of Life of chronic obstructive pulmonary disease patients after a 1-year téléherabilitaion versus standard care program, after an initial short-term pulmonary rehabilitation program
Quality of life assessed by the Saint Georges Respiratory Questionnaire. Three scores are calculated for the components: Symptoms; Activities; Impacts. A Total SCORE is also calculated. The minimum significant difference is 4 points.

Secondary Outcome Measures

Pre-intentional variables
Perceived risk: questionnaire focused on respiratory disease and conditioned by absence of adoption of physical activity behavior. Expectation of conséquences: questionnaire of the expected effects of Physical activity on physical health and psychological well-being. Self-efficacy: questionnaire relating to their perceived ability to perform the quantity of physical activity recommended by healthcare professionals. Intentions: determination and realization of physical activity behavior in the next months.
Post-intentional variables
planning: by a Questionnaire relating to the anticipation of the conditions to realize physical activity. self-efficacy with regard to barriers: questionnaire relating to their perceived ability to perform physical activity recommended despite the difficulties encountered. Social support:questionnaire relating to the behavior of the entourage habits: questionnaire on automatic nature of physical activity behavior.
Physical Activity behaviors.
Measured by the International Physical Activity Questionnaire as a continuous variable (MET minutes a week). MET minutes represent the amount of energy expended carrying out physical activity. walking consider to be 3.3 METS, moderate physical activity to be 4 METS and vigorous physical activity to be 8 METS.
Predictive model of physical activity behavior
Test a predictive model of physical activity behavior at 12 months in each of the two arm groups.

Full Information

First Posted
June 29, 2020
Last Updated
September 13, 2023
Sponsor
University Hospital, Montpellier
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1. Study Identification

Unique Protocol Identification Number
NCT04550741
Brief Title
Long-term Maintenance Benefits of a Pulmonary Rehabilitation Program Using a Mobile Digital Solution: a Prospective, Randomized, Controlled, Multicenter Study in a Population of COPD Patients
Acronym
m-Rehab COPD
Official Title
Long-term Maintenance Benefits of a Pulmonary Rehabilitation Program Using a Mobile Digital Solution: a Prospective, Randomized, Controlled, Multicenter Study in a Population of COPD Patients
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 10, 2022 (Actual)
Primary Completion Date
October 1, 2024 (Anticipated)
Study Completion Date
May 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic obstructive pulmonary disease (COPD) is a public health problem: high prevalence; increasing morbidity and mortality; impact on health costs. Pulmonary rehabilitation (PR) is a multidisciplinary intervention combining exercise training, therapeutic education, psychosocial and behavioral interventions. Its effects are beneficial in the short and medium terms but are limited in time, between 6 and 12 months, for patients who do not pursue regular physical activity (PA) in post-rehabilitation and who do not adopt behavioral changes for health, by loss of motivation. Maintaining the long-term benefits acquired during a short-term PR program is therefore a major issue in the management of COPD. The recent development of remote rehabilitation is a promising approach that has been studied in few studies. In a randomized, controlled and multicenter study, we propose to test the hypothesis that the use of a mobile telerehabilitation solution will allow COPD patients to mainain at long-term the benefits acquired during a short-temr programm and therfore improve their quality of life. (PA) in post-rehabilitation and who do not adopt behavioral changes for health, by loss of motivation. Maintaining the long-term benefits acquired during a short-term PR program is therefore a major issue in the management of COPD. The recent development of remote rehabilitation is a promising approach that has been studied in few studies. In a randomized, controlled and multicenter study, we propose to test the hypothesis that the use of a mobile telerehabilitation solution will allow COPD patients to mainain at long-term the benefits acquired during a short-temr programm and therfore improve their quality of life.
Detailed Description
Exclusion criteria: Presence of contraindications for exercise training (neuromuscular disease, orthopedic cause). Patients with significant and unstable cardiovascular disease. Inability to understand and/or answer questionnaires. Refusal to use a smartphone or digital device. Unable to access an internet connection at home. Analysis: The main analysis will be the univariate intention-to-treat analysis of the primary outcome. Secondary analyzes will include: Analysis with intention to treat secondary endpoints. Multivariate analysis of the efficiency criteria. Univariate and multivariate medico - economic cost - utility analyzes, with their respective sensitivity analyzes. Protocol: This prospective, randomized study with two parallel arms, controlled against standard chronic care will be multicentric and open. Patients included will be patients diagnosed with COPD who are on RR for four weeks in one of the three centers participating in the study. Participation in the study will be offered after verification of the eligibility criteria, during the 3rd week of the stay. The information note will then be provided to them. After obtaining consent, the volunteers will be included in the study at the start of the 4th week and randomized into two arms: - Experimental group of 100 patients using the M-Réhab BPCO telerehabilitation solution. The solution will be provided during the fourth and final week of RR's stay during which patients will be trained to use all of the solution's features. Patients will carry out the entire post-rehabilitation using the remote rehabilitation solution and will benefit from medical assessments by teleconsultation at 1, 3, 6 and 12 months as well as assessments at 3, 6 and 12 months by filling. electronic auto-questionnaires followed by a telephone quality control if necessary. A final evaluation at 12 months, by videoconference, will be carried out at the patient's home. Control group of 100 patients following usual standard chronic care. Patients will receive during the last week of stay in the center, the usual advice to continue physical activity and nutritional advice at home. The evaluations at 3, 6 and 12 months will be done by electronic filling of auto-questionnaires followed by a telephone quality control if necessary. A final evaluation at 12 months, by videoconference, will be carried out at the patient's home. The duration of the inclusions is 18 months and the follow-up will be carried out over 12 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
Chronic obstructive pulmonary disease, Telerehabilitation, Telemedicine, Exercise training, Quality of life, E-health, Connected objects, Care manager

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
This study will be an Open study. For the primary outcome the analysis will be blind to the investigator
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Telerehabilitation
Arm Type
Experimental
Arm Description
Experimental group of 100 patients using the M-Réhab BPCO telerehabilitation solution. The solution will be provided during the fourth and final week of RR's stay during which patients will be trained to use all of the solution's features. Patients will carry out the entire post-rehabilitation using the remote rehabilitation solution and will benefit from medical assessments by teleconsultation at 1, 3, 6 and 12 months as well as assessments at 3, 6 and 12 months by filling. electronic auto-questionnaires followed by a telephone quality control if necessary. A final evaluation at 12 months, by videoconference, will be carried out at the patient's home.
Arm Title
Standard chronic care
Arm Type
No Intervention
Arm Description
following usual standard chronic care. Patients will receive during the last week of stay in the center, the usual advice to continue physical activity and nutritional advice at home. The evaluations at 3, 6 and 12 months will be done by electronic filling of auto-questionnaires followed by a telephone quality control if necessary. A final evaluation at 12 months, by videoconference, will be carried out at the patient's home.
Intervention Type
Other
Intervention Name(s)
telerehabilitation
Other Intervention Name(s)
Digital solution of telerehabilitation with remote connected objects
Intervention Description
After obtaining consent, the volunteers will be included in the study at the start of the 4th week and randomized into two arms: Experimental and Control group
Primary Outcome Measure Information:
Title
Quality of Life of chronic obstructive pulmonary disease patients after a 1-year téléherabilitaion versus standard care program, after an initial short-term pulmonary rehabilitation program
Description
Quality of life assessed by the Saint Georges Respiratory Questionnaire. Three scores are calculated for the components: Symptoms; Activities; Impacts. A Total SCORE is also calculated. The minimum significant difference is 4 points.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Pre-intentional variables
Description
Perceived risk: questionnaire focused on respiratory disease and conditioned by absence of adoption of physical activity behavior. Expectation of conséquences: questionnaire of the expected effects of Physical activity on physical health and psychological well-being. Self-efficacy: questionnaire relating to their perceived ability to perform the quantity of physical activity recommended by healthcare professionals. Intentions: determination and realization of physical activity behavior in the next months.
Time Frame
baseline
Title
Post-intentional variables
Description
planning: by a Questionnaire relating to the anticipation of the conditions to realize physical activity. self-efficacy with regard to barriers: questionnaire relating to their perceived ability to perform physical activity recommended despite the difficulties encountered. Social support:questionnaire relating to the behavior of the entourage habits: questionnaire on automatic nature of physical activity behavior.
Time Frame
6 months
Title
Physical Activity behaviors.
Description
Measured by the International Physical Activity Questionnaire as a continuous variable (MET minutes a week). MET minutes represent the amount of energy expended carrying out physical activity. walking consider to be 3.3 METS, moderate physical activity to be 4 METS and vigorous physical activity to be 8 METS.
Time Frame
12 months
Title
Predictive model of physical activity behavior
Description
Test a predictive model of physical activity behavior at 12 months in each of the two arm groups.
Time Frame
At 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
78 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed with COPD according to the GOLD (Global Initiative for Chronic Obstructive Lung Disease) creteria. Presence of an incompletely reversible obstructive ventilatory disorder defined by a report VEMS / CVF lower than the lower limit of normal post-bronchodilator. Patient on RR for four weeks in respiratory rehabilitation center. Aged between 40 and 78 years. Exclusion Criteria: Presence of contraindications for exercise training (neuromuscular disease, orthopedic cause). Patients with significant and unstable cardiovascular disease. Inability to understand and/or answer questionnaires. Refusal to use a smartphone or digital device. Unable to access an internet connection at home.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Maurice HAYOT, MD, PhD
Phone
+33 467 335 908
Email
m-hayot@chu-montpellier.fr
Facility Information:
Facility Name
Centre hopsitalier universitaire de Montpellier
City
Montpellier
State/Province
Occitanie
ZIP/Postal Code
34295
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maurice HAYOT, MD, PhD
Phone
+33 467 335 908
Email
m-hayot@chu-montpellier.fr
Facility Name
Clinique du Souffle
City
Osséja
ZIP/Postal Code
66340
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julie BLANC MAURIN, Dr
Phone
(+33)6.65.84.96.49
First Name & Middle Initial & Last Name & Degree
Séverine MANANDISE
Phone
(+33)6.65.84.96.49
Email
severine.manandise@korian.fr

12. IPD Sharing Statement

Citations:
PubMed Identifier
33511633
Citation
Cox NS, Dal Corso S, Hansen H, McDonald CF, Hill CJ, Zanaboni P, Alison JA, O'Halloran P, Macdonald H, Holland AE. Telerehabilitation for chronic respiratory disease. Cochrane Database Syst Rev. 2021 Jan 29;1(1):CD013040. doi: 10.1002/14651858.CD013040.pub2.
Results Reference
derived

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Long-term Maintenance Benefits of a Pulmonary Rehabilitation Program Using a Mobile Digital Solution: a Prospective, Randomized, Controlled, Multicenter Study in a Population of COPD Patients

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