- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05385341
Rehabilitation Exercise With MObile Technology and Education After Acute Coronary Syndrome (REMOTE-ACS)
Is Tele-rehabilitation an Efficacious Alternative to Traditional Center Based Cardiac Rehabilitation After Acute Coronary Syndrome?
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
After acute coronary syndrome (ACS), it is recommended to propose a cardiac rehabilitation (CR) program in order to reduce the risk of recidive, to improve the quality of life and to reduce the risk of disabilities. Traditional CR which is most of the time center-based, is underutilized with less than 30% of patients addressed en France. Therefore, Télé-Cardiac Rehabilitation (Télé-RCV) has been developped progressively since the eighties showing comparable efficacity compared with CR concerning physical fitness. The investigative team, had previously published results showing that telephone support guided by accelerometers could improve physical activity. However, In France, device allowing telemonitoring online of heart rate are not available. Moreover, the investigators have not yet developped remote therapeutic education which is proposed in CR programs. Thus, the present study planned to develop and evaluate aTele-RCV solution aimed to monitor exercise training at home and to educate remotely patient after ACS.
The device is an association of a heart rate monitor, a blood pressure testing, a balance linked with a full web secured application connecting patient and caregivers. In the intervention group, Tele-RCV is proposed during 20 sessions containing 2h of exercise training combined with 6h of therapeutic tele-education. In the control group, CR is proposed during 20 sessions with the same volume of exercise training and therapeutic education. After randomisation, patient are allocated to one of the two groups. The evaluation of the primary and secondary outcomes are realized at the beginning, at one month (only walking tests) and at 2 months. A social evaluation is done in parallel to test the acceptability for the Télé-RCV compared with CR.
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Toulouse, France
- Marc LABRUNEE
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patient with acute coronary syndrome less than 6 months,
- Addressed to ambulatory cardiac rehabilitation,
- Equipped with a smartphone compatible with the protocol's application, connected to web
- Having signed an informed consent,
- Affiliated to the french national health insurance.
Exclusion Criteria:
- Incapacity to use application on smartphone,
- Contraindication to exercise training,
- Pregnancy,
- Juridic protection
- Left ventricular ejection fraction < 45%
- Significate ventricular arrhythmia (frequent or polymorph PVC during initial exercise testing, ventricular tachycardia or sudden cardiac death at the beginning)
- Flutter or atrial fibrillation (transient or permanent)
- Coronary revascularization needing supplementary procedure
- Residual myocardial ischemia determined by initial exercise testing or alternative testing (nuclear imaging or stress echocardiography)
- Mini Mental State < 26
- Patients living alone at home
- Comorbidities limiting participation to the protocol: kidney dialysis, insulin-requiring diabetes, residuals sequels of central and/or peripheral nervous system injuries
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Telerehabilitation (Tele RCV)
Experimental group (Tele-RCV): the treatment will consist of 20 home-based sessions monitored by the REMOTE-ACS device and containing 2 hours/day 5 days/7 of exercise training (the first session in center to form the patient) associated with 8 educative sessions.
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20 home-based sessions monitored by the REMOTE-ACS device and containing 2 hours/day 5 days/7 of exercise training associated with educative sessions.
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Active Comparator: Rehabilitation (RCV)
Group control (RCV) : 20 sessions of cardiac rehabilitation will be realized in a rehabilitation center containing exercise training during 2 hours/day 5 days/7 and educative program.
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20 sessions of cardiac rehabilitation will be realized in a rehabilitation center containing exercise training during 2 hours/day 5 days/7 and educative program.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Effect analysis 2 month after inclusion
Time Frame: 2 months
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Change of the peak oxygen volume at 2 months after inclusion
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2 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Effect analysis 1 month after inclusion
Time Frame: 1 month
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Analysis of change between T0 and 1 month concerning the walking tests : distance traveled in meters
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1 month
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Effect analysis 1 month after inclusion
Time Frame: 1 month
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Analysis of change between T0 and 1 month concerning the number of Tele-RCV or RCV sessions realized
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1 month
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Effect analysis 2 months after inclusion
Time Frame: 2 months
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Analysis of change between T0 and 2 months concerning the walking tests:distance traveled in meters
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2 months
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Effect analysis 2 months after inclusion
Time Frame: 2 months
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Analysis of change between T0 and 2 months concerning the number of Tele-RCV or RCV sessions realized
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2 months
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Health economics criteria
Time Frame: 26 months
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Incremental Cost-effectiveness ratios of the REMOTE-ACS device compared with the traditional cardiac rehabilitation after acute coronary syndrome according to the French national health insurance perspective and 2 months follow-up period.
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26 months
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Health economics criteria
Time Frame: 26 months
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Cost-utility ratios of the REMOTE-ACS device compared with the traditional cardiac rehabilitation after acute coronary syndrome according to the French national health insurance perspective and 2 months follow-up period.
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26 months
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Production cost of the REMOTE-ACS device
Time Frame: 26 months
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Production cost of the REMOTE-ACS device by micro costing, according the hospital perspective
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26 months
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Acceptability of the device
Time Frame: 26 months
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The acceptability will be assessed by a sociological point of view based on collective meeting (with patient and caregivers) and individual questionnaires for the two groups before randomization and after the program only for the Tele-RCV group.
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26 months
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Satisfaction of the device
Time Frame: 26 months
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The satisfaction will be assessed by a questionnaire of satisfaction titled: Cardiovascular rehabilitation program satisfaction questionnaire, with 8 questions, the minimum value is "nothing", and the maximum value is "very important"
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26 months
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Marc LABRUNEE, MD, University Hospital, Toulouse
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RC31/18/0474
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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