Patients living with HIV (PLWHIV) have compromised muscle metaboreflex, which can cause exercise intolerance. This randomized controlled clinical trial will verify the effects of regular exercise on autonomic and hemodynamic responses to muscle ergoreflex activation in these patients. PLWHIV without regular physical exercise will be randomly assigned into an exercise training or a control group. The exercise training group will undergo regular physical exercise during 12 weeks (60-min session performed 3 times/wk with moderate intensity), while the control group will keep inactive. Another group consisted of inactive HIV-uninfected group will be included. The primary endpoints will be blood pressure and autonomic markers in response to the Stroop Color-Word Test and the activation of muscle ergoreflex, by means of the post-exercise circulatory arrest (PECA), which will be performed with and without the topical application of a capsaicin-based analgesic balm. Secondary endpoints will include heart rate, peripheral vascular resistance, stroke volume, cardiac output, blood lactate concentration, anthropometrics, and handgrip strength. The active and inactive PLWHIV groups will be evaluated before and after the exercise training, while the healthy group only at baseline.
HIV-infection is associated to a reduced maximal cardiac output and blunted pressor reflex response to static handgrip exercise, which are suggestive of impaired ergoreflex activation. An abnormal ergoreflex activation may lead to exercise intolerance and increases in cardiovascular risk. Despite the importance of therapeutic strategies in reducing the cardiovascular risk among patients living with HIV, exercise-related effects on ergoreflex sensitivity in these population have not been previously investigated.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Enrollment
63
Exercise training performed during 12 weeks, 3 sessions per week of 60 minutes of strength and aerobic exercises.
Rio de Janeiro State University
Rio de Janeiro, Rio de Janeiro, Brazil
RECRUITINGChange from Baseline Blood Pressure at 3 months
Blood pressure will be assessed by a digital sphygmomanometer.
Time frame: Baseline and 3 months of follow-up
Change from Baseline Heart Rate Variability at 3 months
Heart rate variability will be assessed by a heart rate monitor.
Time frame: Baseline and 3 months of follow-up
Change from Baseline Heart Rate at 3 months
Heart rate will be evaluated beat-to-beat by means of a heart rate monitor.
Time frame: Baseline and 3 months of follow-up
Change from Baseline Peripheral Vascular Resistance at 3 months
Peripheral Vascular Resistance will be evaluated by photpletismography.
Time frame: Baseline and 3 months of follow-up
Change from Baseline Stroke Volume at 3 months
Stroke Volume will be evaluated by photoplethysmography.
Time frame: Baseline and 3 months of follow-up
Change from Baseline Cardiac Output at 3 months
Cardiac Output will be evaluated by photoplethysmography.
Time frame: Baseline and 3 months of follow-up
Change from Baseline Blood Lactate at 3 months
Blood Lactate will be determined by the YSL 2700 analyzer.
Time frame: Baseline and 3 months of follow-up.
Change from Baseline Anthropometric markers at 3 months
Anthropometric markers will be determined by a digital scale and wall-mounted stadiometer.
Time frame: Baseline and 3 months of follow-up.
Change from Baseline handgrip maximal voluntary contraction at 3 months
Handgrip maximal voluntary contraction will be assessed using a hydraulic handgrip dynamometer.
Time frame: Baseline and 3 months of follow-up.
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