Healthy Clinical Trial
Official title:
Acute Effects of Whole Body Vibration on Autonomic Function in Healthy Young and Elderly
Verified date | December 2017 |
Source | Universidade Federal de Pernambuco |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Aging causes anatomical and physiological changes in the cardiovascular system and autonomic function with decline in its maximum function. This study aimed to evaluate the acute effects of whole body vibration on cardiovascular system, autonomic function and heart variability in healthy young and elderly. The investigators' hypothesis is that whole body vibration has different effects in young and elderly.
Status | Completed |
Enrollment | 35 |
Est. completion date | December 30, 2017 |
Est. primary completion date | August 31, 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Elderly individuals aged between 60 and 80 years - Young individuals aged between 18 and 30 years - Able to walk without assistance - Good understanding to perform the proposed procedures - Sedentary or low active Exclusion Criteria: - Body Mass Index (BMI) > 35Kg/m2 - Systolic blood pressure > 140 mmHg or diastolic blood pressure > 90 mmHg (at rest) - Difficulty adapting to the whole body vibration - Smoking - Neuromuscular or degenerative disorders - Neurological diseases - Cardiopulmonary comorbidities - Cardiac arrhythmias - Osteoarticular disorders - Use of hormone replacement therapy - Use medications or supplements known to affect cardiovascular parameters - Labyrinthitis |
Country | Name | City | State |
---|---|---|---|
Brazil | Federal University of Pernambuco | Recife | Pernambuco |
Lead Sponsor | Collaborator |
---|---|
Universidade Federal de Pernambuco |
Brazil,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Autonomic Function | Heart rate variability will be assessed from 3-channel holter | Change from Baseline Heart rate variability at 5, 10, 15, 20 and 35 minutes | |
Secondary | Sympathetic modulation | Sympathetic modulation will be assessed from 3-channel holter | Change from Baseline Sympathetic modulation at 5, 10, 15, 20 and 35 minutes | |
Secondary | Parasympathetic modulation | Parasympathetic modulation will be assessed from 3-channel holter | Change from Baseline Parasympathetic modulation at 5, 10, 15, 20 and 35 minutes | |
Secondary | Sympathovagal Balance | Sympathovagal Balance will be assessed from 3-channel holter | Change from Baseline Sympathovagal balance at 5, 10, 15, 20 and 35 minutes | |
Secondary | Heart Rate | Non-invasive measures will be assessed from 3-channel holter | Change from Baseline Heart Rate at 5, 10, 15, 20 and 35 minutes | |
Secondary | Blood pressure | Non-invasive measures of brachial blood pressure | Change from Baseline Blood pressure at 5, 10, 15, 20 and 35 minutes | |
Secondary | Peripheral oxygen saturation | Non-invasive measures will be assessed from pulse oximeter | Change from Baseline Peripheral oxygen saturation at 5, 10, 15, 20 and 35 minutes | |
Secondary | Adverse effects | Adverse effects reported by volunteers | Change from Baseline at 20 minutes |
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