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Hypertension (HBP)

About Hypertension (HBP) Clinical Trials (Click to Open)

Join Clinical Trials for Hypertension

Clinical Trials for HypertensionGeneral Purpose:

High blood pressure (HBP) is a common condition affecting almost one third of America and increases an individual’s risk for developing such serious health problems as heart disease and heart failure. There will be different trial purposes depending on the stage of HBP.

For example, if you are pre-hypertensive, clinical trials will be targeted at preventing your condition from developing into stage 1 or 2 HBP. Many questions remain about the development of HBP and treatments, so clinical research aims to learn more about HBP.

Some studies are trying to determine the potential affects of HBP and treatments for HBP on brain functioning in children. There are many trials trying to uncover new and improved behavioral interventions for treating HBP.

Observational studies conducted to expand our understanding of the underlying epidemiology of HBP are attempting to look at the role that stress, SES, ethnicity, and other related factors play on blood pressure. There is also a great deal of research being conducted on the potential positive impact of medications and therapeutic treatments on controlling blood pressure.

By taking part in a clinical trial for hypertension (HBP), you will be among the first to obtain new treatments that may improve your health and quality of life. You will also be helping improve the scientific body of data surrounding this widespread condition.

What will Clinical Trials for Hypertension be like?

These trials intend to learn more about HBP, to facilitate prevention and treatment. Before joining a clinical trial, researchers will first assess your eligibility for helping achieve that end. You will go through a screening phase to ensure that you are an appropriate participant for the aims of the trial. Inclusion criteria are intended to provide benefit and avoid wasting your time.

They are also put in place to avoid any risk of a detrimental interaction between a behavioral or pharmaceutical intervention and an existing condition or medication. The researchers will therefore ask you to provide a very detailed medical history and perform clinical assessments to learn the state of your condition.

They will likely need such baseline information as height, weight, BMI, and may require urine and blood samples. Observational studies will likely have certain background restrictions for inclusion, such as ethnicity or age, in order to focus on certain epidemiologic trends.

Interventional studies will first require participants to undergo in depth screening, including blood pressure measurements. These inclusion criteria intend to determine if you are a good candidate for various forms of intervention, from behavioral to pharmaceutical.

Typical Hypertension Clinical Trial Protocol:

As with all clinical research, the trial protocol will depend upon the condition phase beingClinical Trials for Hypertension studied, as well as the treatment or observation being measured. Interventional trials evaluating a pharmaceutical will first randomly assign participants to different groups, either receiving a varying dose of a drug or a placebo.

Participants will then receive follow up assessments of blood pressure, metabolic factors, cardiovascular risk, etc. at specified time points throughout the duration of the study. While participating in these interventional studies, you will receive cardiovascular care and monitoring. Observational studies conducted to evaluate environmental risk factors, such as stress, will monitor your physiological functioning.

This might include spending nights at an associated clinical research hospital for sleep monitoring to obtain breathing rates and various physical movements. Blood pressure at a resting state and while performing certain activities will also help enhance scientific knowledge about HBP.

Given the impact of behavior on HBP, participants in behavioral intervention trials will undergo relevant baseline assessments, and after beginning a treatment (such as dietary changes and/or exercise) will continuously receive physiological monitoring to assess the benefit of the intervention being studied.

All clinical trials will attempt to provide you personal benefit that improves your quality of life, while also using information provided by your trial experience for the betterment of the many Americans struggling with HBP.  

Suggested Search Terms:

Impact of Stress on High Blood Pressure, Relationship Between Ethnicity and Blood Pressure, Controlling High Blood Pressure with Medication, Benefit of Exercise on High Blood Pressure, High Blood Pressure in Children

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