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Valiance Clinical Research
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Now Enrolling — Tarzana, CA
HIGH BLOOD PRESSURE STUDY
Help Advance Hypertension Research While Receiving Care at No Cost
If you have been diagnosed with cardiovascular disease or are 55+ with uncontrolled high blood pressure, you may qualify. Fill out the form below to see if you're eligible, it only takes a minute.
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About This Study
Learn more about the hypertension research study while you wait
Study Purpose
Evaluating Innovative Hypertension Treatments
This clinical trial investigates new approaches to controlling high blood pressure and reducing cardiovascular risk in adults with established heart disease or those at high risk.
Location
Tarzana, California
All study visits will take place at our state-of-the-art research facility in Tarzana, CA. Free transportation to and from the site is provided for all participants.
Study Status
Now Enrolling
We are actively enrolling qualified participants. Our team is reviewing applications and conducting screenings on an ongoing basis.
Medication Schedule
Every 6 Months
Study medication will be administered every 6 months during your scheduled visits, with regular monitoring and follow-up care throughout the trial.
Participant Benefits
Comprehensive support for all qualified participants
$50–$250 Compensation Per Visit
Receive compensation for each completed study visit, recognizing your valuable time and contribution to advancing medical research.
Free Transportation
Complimentary transportation to and from our Tarzana, CA research site for all scheduled visits. Never worry about travel logistics.
No-Cost Medical Care
All study-related medication, examinations, and medical care provided at no cost to participants throughout the entire trial.
Comprehensive Health Monitoring
Regular blood pressure checks, cardiovascular assessments, and professional medical oversight throughout your participation.
Expert Medical Team
Access to experienced research physicians and study coordinators who are dedicated to your safety and well-being.
Contribute to Medical Science
Help advance hypertension research and potentially improve treatments for future patients with cardiovascular conditions.
Study Eligibility Criteria
For your reference, here are the general eligibility criteria for this study. Final eligibility will be determined during your screening visit.
- Adults 18 years and older with established cardiovascular disease (such as previous heart attack, stroke, or other heart conditions)
- Adults over 55 years old with a risk of cardiovascular disease (CVD) and uncontrolled high blood pressure
Note: These are general guidelines. Our medical team will conduct a comprehensive evaluation to determine your eligibility for the study.
The Complete Study Journey
What to expect from screening through completion
1
Initial Contact & Phone Screening
Our study coordinator will contact you for a brief phone conversation.
- Receive a call within 1-2 business days
- Brief phone screening (5-10 minutes)
- Answer basic health and eligibility questions
- Ask any initial questions you may have
2
Screening Visit
If eligible based on your phone screening, you'll be invited to our Tarzana facility for a comprehensive evaluation.
- Meet the research team and tour our facility
- Review detailed study information and informed consent
- Complete medical history questionnaire
- Physical examination and vital signs
- Blood pressure measurements
- Laboratory work (blood tests if needed)
- Determine final eligibility for the study
3
Enrollment & Consent
If you qualify and choose to participate, you'll officially enroll in the study.
- Sign the informed consent form after all questions are answered
- Receive your study information packet
- Schedule your first study visit
- Get contact information for 24/7 study support
4
Study Participation
Attend regular monitoring appointments and receive study medication every 6 months.
- Receive study medication as scheduled
- Regular blood pressure monitoring and health assessments
- Report any changes in your health or medications
- Complete questionnaires about your well-being
- Receive compensation for each completed visit
- Maintain communication with study team between visits
5
Study Completion
Complete your final study visit and receive information about next steps.
- Final health assessment and evaluation
- Discussion of study results and findings
- Recommendations for ongoing care
- Information about accessing treatment after study (if applicable)
- Receive final compensation
Frequently Asked Questions
Browse our comprehensive FAQ while you wait for our call
What is a clinical trial?
A clinical trial is a research study that tests new treatments, medications, or medical approaches to determine their safety and effectiveness. Clinical trials follow strict scientific standards and are closely monitored by medical professionals and regulatory agencies to protect participants. They are essential for advancing medical science and developing new treatments for various health conditions.
Why should I consider participating in a clinical trial?
Participating in a clinical trial offers several benefits: you receive high-quality medical care at no cost, gain access to innovative treatments before they become widely available, contribute to medical science that may help future patients, receive close monitoring from medical professionals, and often receive compensation for your time and commitment. Many participants also find the experience personally rewarding knowing they're helping advance healthcare.
Is participation in a clinical trial safe?
Yes. All clinical trials follow strict safety protocols approved by an Institutional Review Board (IRB), which is an independent committee that reviews research to protect participants' rights and welfare. Participants are closely monitored throughout the study by medical professionals, and you can withdraw at any time if you feel uncomfortable. Before enrolling, you'll receive detailed information about potential risks and benefits, and you'll have the opportunity to ask questions.
What does this hypertension study involve?
This study evaluates innovative treatments for high blood pressure in adults with cardiovascular disease or at risk for it. Participation involves regular visits to our Tarzana facility for blood pressure monitoring, health assessments, and receiving study medication every 6 months. You'll be closely monitored by our medical team throughout the study to ensure your safety and track the effectiveness of the treatment.
Can I continue seeing my regular doctor during the study?
Yes! We encourage you to maintain your relationship with your primary care physician and other healthcare providers. With your permission, we will coordinate with your regular doctors to ensure continuity of care. It's important that you inform both your regular doctor and our study team about any changes in your health or medications.
Where does the study take place?
All study visits take place at our state-of-the-art research facility in Tarzana, California. The facility is designed specifically for clinical research and includes comfortable examination rooms, modern medical equipment, and a professional team dedicated to participant care. Free parking is available, and we also provide complimentary transportation to and from the site for all study visits.
Do I qualify if I'm already taking blood pressure medication?
Many participants in our study are currently taking blood pressure medication. In fact, being on medication doesn't automatically disqualify you. During your screening visit, our medical team will review all your current medications and health conditions to determine if you're eligible for the study. It's important to be open about all medications and supplements you're taking.
What if I have other health conditions besides high blood pressure?
Having other health conditions doesn't necessarily disqualify you from participating. Many people with multiple health conditions successfully participate in clinical trials. During the screening process, our medical team will conduct a comprehensive review of your complete medical history to determine if the study is appropriate for you. We consider each potential participant individually to ensure their safety.
I'm over 65 years old. Can I still participate?
Yes! There is no upper age limit for this study. In fact, we specifically welcome participants over 55 years old who have cardiovascular risk factors and uncontrolled high blood pressure. Age alone is not a disqualifying factor. What matters most is your overall health status and whether the study is appropriate for your specific medical situation.
How much compensation will I receive?
Qualified participants receive between $50 and $250 per completed study visit. The exact amount depends on the type of visit and the procedures involved. Some visits may involve more tests or take longer, resulting in higher compensation. You'll be informed about the compensation for each visit type during the enrollment process.
Is parking available at the facility?
Yes, free parking is available at our Tarzana facility for all study participants. Additionally, if you prefer not to drive or don't have access to transportation, we provide complimentary transportation to and from the research site for all scheduled study visits. Simply let us know your transportation needs when scheduling your appointments.
What if I need to miss a scheduled visit?
We understand that life happens and unexpected situations arise. If you need to miss a scheduled visit, please contact our study coordinator as soon as possible so we can reschedule. However, please note that consistently missing visits may affect your eligibility to continue in the study, as regular monitoring is important for both your safety and the integrity of the research.
What medication will I receive in this study?
The specific study medication and detailed information about how it works will be thoroughly explained during your screening visit and before you sign the informed consent form. This allows you to make an informed decision about participation. Our study doctor will discuss the medication's mechanism of action, how it's administered, and what to expect.
Are there side effects I should be aware of?
All medications can potentially cause side effects. Before you begin the study, the study doctor will discuss in detail all known and potential side effects of the study medication. You'll receive written information about what to watch for and what to do if you experience any side effects. Throughout the study, you'll be closely monitored, and you should report any symptoms or concerns to the study team immediately.
What if I experience side effects during the study?
If you experience any side effects, contact the study team immediately. You will have 24/7 access to a study physician who can address your concerns and provide medical guidance. Your safety is our top priority. If necessary, you may be asked to come in for an unscheduled visit to be evaluated. Remember, you can also withdraw from the study at any time if you're uncomfortable continuing.
How often will I receive the study medication?
In this study, medication is administered every 6 months during your scheduled study visits. Between medication visits, you'll have regular monitoring appointments to check your blood pressure and overall health. The study team will provide you with a complete schedule of all visits during the enrollment process.
Can I leave the study if I change my mind?
Absolutely. Participation in clinical research is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you're otherwise entitled. If you choose to withdraw, simply inform the study team. We may ask you to complete a final safety visit to ensure your health is stable, but this is not required.
Will my personal information be kept confidential?
Yes. All your medical information and personal data are protected under HIPAA regulations and are kept strictly confidential. Your name will never be used in any publications or presentations of study results. Data used for research purposes is de-identified, meaning it cannot be traced back to you personally. Only authorized study staff have access to your identifiable information, and all data is stored securely.
What is an Informed Consent Form?
The Informed Consent Form is a detailed document that explains everything about the study, including its purpose, procedures, potential risks and benefits, your rights as a participant, and alternatives to participation. Before signing, you'll have ample time to review the document, discuss it with family or friends if you wish, and ask the study team any questions you have. Signing the consent form means you understand the study and agree to participate, but you can still withdraw at any time afterward.
Who oversees the study to ensure participant safety?
All clinical trials are overseen by an Institutional Review Board (IRB), which is an independent committee of medical professionals, researchers, and community members who review the research protocol to protect participants' rights and welfare. The IRB reviews the study before it begins and continues to monitor it throughout. Additionally, the study is conducted according to Good Clinical Practice (GCP) guidelines and is subject to FDA regulations.
What happens to my health information after the study ends?
After the study concludes, your health information continues to be protected under HIPAA regulations and is stored securely. De-identified data may be used for research purposes, such as publishing study results in medical journals, but this data cannot be traced back to you. You'll receive your personal health information collected during the study, and overall study results are typically made available after analysis is complete.
Have Questions While You Wait?
We're here to help. Feel free to reach out if you have any questions before we call you.
