Postexercise Hypotension Clinical Trial
— CAPEROfficial title:
Postexercise Hemodynamics Compared in Obese and Non-Obese Subjects After Aerobic Interval Training
Verified date | February 2020 |
Source | Arizona State University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study examines the effect of obesity and gender on postexercise hypotension with three different randomized exercise protocols or varying intensity. Subjects will be separated into obese and non-obese groups and then further by gender. From there, they will be put through a control, continuous exercise bout, and aerobic interval bout of exercise in a randomized order over three visits. Post exercise blood pressure, as well as other non-invasive cardiac measures will be taken over a 4 hour period.
Status | Terminated |
Enrollment | 6 |
Est. completion date | February 7, 2020 |
Est. primary completion date | February 7, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 55 Years |
Eligibility |
Inclusion Criteria: - Healthy, inactive (defined as less than 60 min of moderate to vigorous physical activity per week) - Men (age 18-45) and non-pregnant women (age 18-55) - Normal BMI and waist circumference (18.5- 24.5 kg/m2 and waist <94 cm ) OR obese (BMI > 30kg/m2 and waist >94 cm). - normotensive or prehypertensive blood pressure (SBP <140 and DBP <90) according to JNC guidelines. Exclusion Criteria: - Subjects over age (men >45, women > 55) - Subjects who register more than 60 minutes/week of moderate-to-vigorous physical activity via accelerometer - Subjects who classify as hypertensive (SBP >140 or DBP >90) - Subjects who answer positively (i.e. yes) on The Physical Activity Readiness Questionnaire (PAR-Q). - Subjects with known cardiovascular, pulmonary, renal, or metabolic disease, or are having symptoms of these disease will be excluded, following current American College of Sports Medicine guidelines (ACSM). - Current smokers - Pregnant women - Anyone with contraindications to vigorous exercise will be excluded from the study. -Subjects on medications used for the treatment of symptomatic cardiovascular disease will be excluded. |
Country | Name | City | State |
---|---|---|---|
United States | Arizona Biocollaborative Building- Healthy Lifestyle research labratory | Phoenix | Arizona |
United States | Arizona Biomedical Collaborative 1 | Phoenix | Arizona |
Lead Sponsor | Collaborator |
---|---|
Arizona State University |
United States,
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* Note: There are 12 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Postexercise Blood pressure | Central and peripheral blood pressure (systolic and diastolic) taken via Oscar 2 device. | Postexercise- every ten minutes for four hours post exercise session | |
Secondary | Heart Rate Variability | Heart rate variability (taken via polar monitor) | until study completion- up to 2 years | |
Secondary | Cardiac Output- non-invasive | Non-invasive: taken via physioflow device | until study completion- up to 2 years | |
Secondary | Systemic Vascular Resistance | Non-Invasive: Taken via physioflow device | until study completion- up to 2 years |
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