Effect of a High-intensity Interval-training on "Heart Rate Variability" Prognostic Parameters in Early Post-stroke Patients: A Randomized Controlled Trial

Brief Summary

Detailed Description

A randomized controlled 2-arms parallel study, comparing HRV in two groups of stroke patients. Post-acute stroke patients hospitalized in rehabilitation stroke¬-units, within secondary care hospitals, are screened for eligibility. * Inclusion criteria: * first-ever hemispheric stroke, with consistent clinical and neuroimaging signs * \<3 month * NIHSS \<20 in acute care * age\>18 * Non-inclusion criteria: * complicated diabetes mellitus with objective neuropathy and/or autonomic dysfunction * other concomitant cardiac or pulmonary diseases possibly affecting HRV recordings, ie: acute myocardial infarction (\<6 month), myocardial dysfunction as severe dilated or hypertrophic cardiomyopathy, class 3 and 4 heart failure, arrhythmias including chronic atrial fibrillation, conduction abnormalities. * beta-blockers with no alternative options * severe cognitive impairment inconsistent with free, informed and written consent or questionnaire filling * Patients will benefit beforehand from a symptom-limited Graded Exercise Test (GXT), with ECG monitoring and using a semi recumbent cycle ergometer (Ergoline, Optibike MED600), mainly to exclude a CV risk and to accurately assess their exercise capacities for better individualized programs. Peak oxygen uptake, Peak Power , Peak Heart Rate, Respiratory Exchange Ratio (VO2peak, Power peak, HRpeak, RER respectively) will be measured, Ventilatory Threshold 1 (VT1) will be estimated, and oxygen uptake, power and heart rate at VT1 will be recorded (VO2vt1, Pvt1, HRvt1). * The standard-of-care neuro-rehabilitation program was carried out according to the international recommendations. It will consist daily in a mean of 3 sessions (2 to 4), five days a week: physiotherapy (with, among others, Strengthening-Stretching activity), occupational therapy, cognitive therapy (orthophonist or neuro-psychologist). In addition, either aerobic training (HIIT) or non-aerobic training (Control Group-CG by Low Intensity Group Training-LIGT). * HIIT and LIGT training volume and duration will be the same (16 sessions, 12 to 30' each, 6 weeks). The intervention-group (HIIT Group) will realize a 6-weeks Aerobic Training as follows: Among the FITT principle: * Frequency: 2-3 times a week * Intensity: long-HIIT: 4 to 5 four-minutes intervals at Pvt1(+/- 2 steps) interspersed with two-minutes interval at 50% Pvt1=(4-5 x (4':2')/(Pvt1 :50%Pvt1)) * short-HIIT: 8 to 10 forty-five seconds intervals at Pmax (+/- 2 steps) interspersed with forty-five seconds rest intervals = (8-10x(45":45")/Pmax :Rest)) * Time: 12' to 30' per session (8 short-sessions of 12 to 15', 8 long-sessions of 24 to 30') * Type: cycling on a semirecumbent ergometer Depending on the patient's fatigue and progress, the intensity will be adjusted, with an HR target \>80% HRpeak during intervals. In the CG group, HIIT will be replaced by "LIGT" sessions, as follows: Among the FITT principle: * Frequency: 2-3 times a week * Intensity: Low HR controlled by HR monitoring (\<50% HRpeak or 30%HRR) * Time: 12' to 30' per session (8 short-sessions of 12 to 15', 8 long-sessions of 24 to 30') * Type: Static and Segmental strengthening and stretching mainly * Measures taken to reduce bias: -Patients' spontaneous physical activity will be monitored via two sets of four-day measurements, including weekends, using an Actigraph device worn on a belt. * The primary endpoint will always be measured over 24 hours, at the same time of week; it will be read blind by the same cardiologist (single-blind). * Known criteria for HRV modification will be monitored (side of the lesion, fever, blood pressure spike or hypoxia during measurement, medication intake). * The other criteria will always be measured during the same half-day. * In order to introduce a "blind component" for the patient (double-blind), the information provided to the patient will specify a "comparison between two different types of physical activity " * At M6, only the primary endpoint will be measured. A Marshall questionnaire will be used at this time to verify the proportion of patients complying with WHO recommendations on physical activity at 6 months post-discharge. Patients who would have been in the control-group will be proposed to enter in an out-patient (day-hospital) HIIT program. * Novelty 1. To use a new and strong risk marker of stroke relapse and post-stroke complications (mortality, morbidity, and poor functional outcomes), which is improved by physical activity, to strengthen the use of Aerobic Training (AT) in secondary prevention. 2. To allow generalization of conclusions: * by studying AT with a shorter intervention-design, limiting competition with neuro-rehabilitation (fatigue, time spent) and via a simple intervention-device (semi recumbent ergometer). (Indeed, most of non-ambulatory participants (82% ) in RCTs benefited from AT through assistive walking devices, using Weight Bearing Support Treadmill, which are difficult to set up (accessibility, personnel and equipment costs…)). * by studying AT effects in a more disabled population and at an early stage. (Indeed, in Randomized Controlled Studies having assessed AT in chronic (\>6months) post-stroke patients, NIHSS ≤ 5/42 was most often chosen for inclusion criterion, with a median NIHSS around 3 at study start.

Primary Outcomes

Secondary Outcomes

• HRV(Week 1, Week 8, Month 6)
• Dose Ratio(Week 2 to Week 7)
• VO2peak(Week1 Vs Week 8)