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Blood Pressure clinical trials

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NCT ID: NCT03698903 Completed - Blood Pressure Clinical Trials

Take a STAND 4 Health: A Sedentary Behavior Reduction Intervention

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

There is emerging evidence that an excessive amount of sitting is linked with an increased risk of negative health outcomes independent of an individual's physical activity levels. This is concerning considering data indicate Americans spend over half of the waking day engaged in sedentary activities, and that individuals who are overweight or obese and/or have a chronic disease such as hypertension are likely to have an even higher level of sedentary behavior. A limited number of experimental studies have looked at the effects of reducing sitting time on blood pressure and have shown promise. However, these studies lasted for only a day, so it is unclear how reducing sedentary time may influence blood pressure over a longer duration. The purpose of this study is to look the relationships between the amount of time a person spends sitting and their blood pressure and examine whether decreasing sedentary behavior helps improve blood pressure. The study employs the use of coaching calls and a mobile health (mHealth) intervention to reduce the sedentary behavior of participants through strategies such as prompting, feedback, and counseling.

NCT ID: NCT03691701 Completed - Hypertension Clinical Trials

Pilot to Examine Risk and Feasibility of Remote Management of BP From Childhood Into Early Adulthood

PERFORMANCE2
Start date: July 20, 2018
Phase: N/A
Study type: Interventional

Hypertension is an increasingly common problem in children, especially among those who are obese or with diabetes and chronic kidney disease. This study is a pilot randomized controlled trial designed to test whether improved blood pressure control can be achieved with the use of remote home blood pressure monitoring in children with uncontrolled blood pressure.

NCT ID: NCT03691194 Completed - Blood Pressure Clinical Trials

The Effects of 8 oz Fresh vs. Commercial Orange Juice on Blood Pressure In Normotensive Males Aged 18-59

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The purpose of this graduate student research study is to determine the effects of drinking eight ounces of fresh vs. commercial orange juice on blood pressure in males with normal blood pressure.

NCT ID: NCT03678116 Completed - Blood Pressure Clinical Trials

Effects of a Thermogenic Dietary Supplement on Metabolic, Hemodynamic, and Mood Responses

Start date: July 23, 2018
Phase: N/A
Study type: Interventional

This a randomized, double blind, placebo controlled, crossover design study which measures the effect of an available thermogenic dietary supplement on resting energy expenditure (REE), blood pressure and heart rate, and mood changes in moderate caffeine consumers. Participants will complete baseline measurements then ingest one of three pills. Once the pill is ingested, subjects will complete four REEs along with heart rate and blood pressure and appropriate questionnaires. Participants will return two more times, each after a one week washout period, and complete the same protocol with the remaining supplements.

NCT ID: NCT03661112 Completed - Blood Pressure Clinical Trials

Wrist-based Blood Pressure Monitoring Study

Start date: May 7, 2018
Phase:
Study type: Observational

To observe blood pressure variation in various real-world settings

NCT ID: NCT03640429 Completed - Obesity Clinical Trials

Accuracy of Non-invasive Blood Pressure Monitoring at the Wrist in Obese Patients

Start date: August 21, 2018
Phase:
Study type: Observational

Arterial blood pressure (ABP) monitoring is a corner stone in perioperative management. However, proper control of SBP requires accurate measurement of ABP. The aim of this work is to validate the wrist OBP monitor in obese patients and compare it to upper arm location (in accuracy, convenience, and trending) using invasive blood pressure monitor as a reference standard.

NCT ID: NCT03634813 Completed - Blood Pressure Clinical Trials

Perioperative Blood Pressure Screening to Improve Long-term Cardiovascular Health

Start date: August 31, 2018
Phase: N/A
Study type: Interventional

To explore in a pilot randomized clinical trial, the impact of Home Blood Pressure Monitoring with patient directed information as compared to usual care on the postoperative management of blood pressure.

NCT ID: NCT03626792 Completed - Physical Activity Clinical Trials

Effect of Mat Pilates Training on Women After Menopause

Start date: August 5, 2017
Phase: N/A
Study type: Interventional

This project aims to verify the chronic effect of Mat Pilates exercise on climacteric symptoms, ambulatory blood pressure responses, lipid and glucose profile and pro and anti-inflammatory and antioxidant markers in postmenopausal normotensive and hypertensive women. All volunteers received the same intervention.

NCT ID: NCT03603860 Completed - Heart Diseases Clinical Trials

Comparison of the Non-invasive Biobeat Device With an Invasive Arterial Line

Start date: November 5, 2018
Phase:
Study type: Observational

In this clinical study the investigators will compare blood pressure measurements obtained using the non-invasive, continuous and wireless Biobeat monitoring device (a wrist watch or a patch configuration) to an invasive arterial line (radial or femoral) in 30 patients immediately after cardiac surgery, at the intensive care unit.

NCT ID: NCT03590080 Completed - Hypertension Clinical Trials

Impact of Intravenous Methylprednisolone Treatment on Blood Pressure

Start date: January 1, 2011
Phase:
Study type: Observational

Hypertension is common side effect of Cushing Syndrome (CS): in patients with endogenous CS and those treated with glucocorticosteroids (GCs). The impact of the intravenous GCs therapy on blood pressure (BP) remains unclear. According to the European Group On Graves' Orbitopathy (EUGOGO), patients with active, severely symptomatic and sight-threatening Graves' orbitopathy (GO) should be treated with high dose intravenous methylprednisolone (IVMP) pulses. There are, however, reports of fatal side effects that may be associated with this therapy (e.g.: pulmonary embolism, myocardial infarction, severe cerebrovascular events, acute liver damage and sudden death). For this reason, the cumulative dose of IVMP should not exceed 8 g within each treatment course, and pulses should not be given on consecutive or alternate days, except for the case of dysthyroid optic neuropathy. A consensus on the monitoring of patients during and after IVMP pulse administration is not yet established. What is more, there is lack of paper regarding pattern of blood pressure at various time points during and after ivGCs administration. Thus, the investigators decided to evaluate acute changes of N-terminal pro-brain natriuretic peptide (NT-proBNP) as a marker of hemodynamic stress and to monitor BP before, during and after IVMP pulse administration. All of patients were treated routinely according to EUGOGO recommendations with standard doses of methylprednisolone with standard recommended schedule. Inclusion criterion for the therapy was according to EUGOGO guidelines active, moderate-to-severe and active GO (12 pulses of IVMP 6x0.5g followed by 6x0.25g every week).