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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: NCT03696654 Recruiting - Blood Pressure Clinical Trials

High Blood Pressure in Paediatric Patients With Sleep Disorder Breathing.

Start date: February 19, 2019
Phase: N/A
Study type: Interventional

There are data supporting a possible increase in the prevalence of High Blood Pressure (HBP) in pediatric patients with Sleep Disorder Breathing (SDB). Adeno-tonsillectomy has proven to be an effective treatment in the correction of nocturnal respiratory events in the majority of patients. Our objective is to determine the presence of HBP in pediatric patients with SDB and the impact of adenotonsillar surgery on its correction. Methodology: 286 children (4-18 years old) will be included consecutively referred for suspected SDB. Variables: a) Clinical history; b) Anthropometric variables: weight, height, body mass index, neck, hip and waist perimeter c) Chervin questionnaire d) polysomnography (PSG) for the SDB assessment and e) for the HBP evaluation, ambulatory blood pressure measurement (ABPM) and pulse transit time (PTT) will be performed during 24h. In control group (not SDB) and patients with indication for medical treatment, the same tests will be repeated six months after the baseline visit. In patients with surgery indication, ABPM and PTT will be performed just before the surgical treatment and ABPM, PTT and PSG six months after the intervention. In a subgroup of patients, will also assess the presence of subclinical organic damage produced by HBP: blood markers (creatinine / glomerular filtration), urine (albuminuria / proteinuria), electrocardiogram and echocardiography (left ventricle hypertrophy).

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: NCT03688503 Active, not recruiting - Blood Pressure Clinical Trials

Magnesium Supplementation and Blood Pressure Reduction

Start date: February 15, 2019
Phase: N/A
Study type: Interventional

This double-blind, placebo-controlled randomized clinical trial will test whether a magnesium glycinate supplement (480 mg/day) taken for 12 weeks lowers 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: NCT03636490 Active, not recruiting - Blood Pressure Clinical Trials

Stress, Salt Excretion, and Nighttime Blood Pressure

SABRE
Start date: November 16, 2018
Phase: N/A
Study type: Interventional

The study will examine urinary sodium excretion induced by psychological stress and its diurnal pattern as a novel biological mechanism that may underlie an abnormal diurnal pattern of blood pressure. The study will test the hypotheses that lower stress-induced sodium excretion is associated with an abnormal diurnal pattern of sodium excretion, and that an abnormal diurnal pattern of sodium excretion is associated with an abnormal diurnal pattern of blood pressure. Primary Aim 1: To examine the association between urinary sodium excretion after provoked psychological stress and the diurnal pattern of sodium excretion. Primary Aim 2: To examine the association between the diurnal pattern of sodium excretion and the diurnal pattern of BP. Secondary Aim: To examine whether the association between urinary sodium excretion after provoked stress and the diurnal pattern of sodium excretion is modified by ecological momentary levels of perceived stress, experienced during the daytime period. Exploratory Aim: To determine the socio-demographic, behavioral, and psychological traits, chronic stress, and biological stress-related factors that are associated with lower stress-induced sodium excretion. Identification of these factors will help determine who is at risk for having a differential sodium excretion response to psychological stress.

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.