Research Studies - Trialsphere

Why Participate

Access to New Treatments: Gain early access to innovative treatments and contribute to the development of new medical therapies.
Indepth healthcare monitoring: Receive free health screenings, lab tests, imaging, and exams, providing valuable insights into your health.
Contribute to Medical Advancements: Play a crucial role in advancing medical knowledge and treatments, helping to improve public health.
Safety and Volunteer Well-being: Enjoy the assurance of a safety-focused environment, with the option to withdraw at anytime for your comfort.

Eligibility Matters: Not all individuals will qualify for every study; eligibility is determined through screening.
Reimbursement for Time and Travel: Reimbursement may be available when provided by the study sponsor.
Privacy and Voluntary Participation: Privacy safeguards followed and participation remains voluntary.

Current Studies

SonusMed Hypertension Study (High Blood Pressure)

Adults aged 21-75 with hypertension (≥140/90 mmHg)
Diagnosed with high blood pressure on at least three separate occasions
NOT taking more than one antihypertensive medication
NOT using weight loss medications (e.g., Ozempic, Mounjaro)

Observation Study for Alzheimer's Disease

Adults aged 60 and older who have undergone testing or screening and have been diagnosed with mild cognitive impairment or mild dementia due to Alzheimer’s disease
Individuals who are considering or are being evaluated for newer treatments for mild cognitive impairment or mild Alzheimer’s disease
Individuals who have a reliable care partner willing to provide written informed consent for participation

Early Cognitive Decline Study

Adults aged 55 to 85 years of age
Have gradual cognitive decline that is noticeable by self or someone close
Have 1 clinical feature of dementia with Lewy-bodies, such as (but not limited to) stiffness, tremor, and/or acting out dreams
Have markers of amyloid-beta and alpha-synuclein found in blood and CSF that meet the study inclusion
Have a reliable study partner

Chronic Migraine Study

Episodic Migraine Study

Upcoming Study

Thank you for your interest in participating in a clinical research study. Please complete the brief form below so our team can identify potential study opportunities and follow up with more information.

By submitting this form, you agree to be contacted by TrialSphere Clinical Research via phone, text, or email. Please do not include sensitive medical information in this form.

FAQs

Everything you need to know

What is a clinical study?

Research studies that evaluate the safety and effectiveness of new medications in humans.
Before human testing, these potential treatments undergo rigorous lab animal testing to verify safety.
They are closely regulated by the US Food and Drug Administration (FDA). FDA approval is required for new treatments, ensuring they meet stringent quality and safety standards before public availability

Why should I join a clinical study?

In-depth Healthcare Attention: Benefit from closer health monitoring and personalized care
from healthcare professionals throughout the study.
Access to New Treatments: Gain early access to innovative treatments and contribute to the
development of new medical therapies.
Complimentary Health Assessments: Receive free health screenings, lab tests, imaging, and
exams, providing valuable insights into your health.
Contribute to Medical Advancements: Play a crucial role in advancing medical knowledge and
treatments, helping to improve public health.
Safety and Volunteer Well-being: Enjoy the assurance of a safety-focused environment, with the
option to withdraw at any time for your comfort.

Can anyone participate in a clinical study?

Yes, however, specific requirements and eligibility criteria exist for participating in clinical studies. Here are some key
things to keep in mind about who can participate:

Age: There are often age minimums and maximums, depending on the study
Health status: To be eligible for the treatment, participants must have the medical condition
that the treatment intends to alleviate. There are usually criteria around the type and severity of
symptoms. Certain other health conditions may also exclude someone from participating if it
could impact results
Gender: Some studies are limited to a single gender, especially early-stage studies testing drugs that
interact differently with men vs. women
Prior treatments/therapies: Another criterion often considered is whether someone has
undergone previous treatments related to the condition

Ultimately, clinical studies set rigorous guidelines on age, health, gender and more. The specifics are
narrowed down based on what they want to test and study for any potential new treatment. Getting
enrolled can be selective.

What are clinical study benefits and study risks?

Benefits include:

Active participation in health care
Difficult to access and often costly treatments
Free testing (i.e. imaging, bloodwork, exams)
Assisting others by participating in studies for potential approval and public availability

Participating in a clinical study may carry risks your doctor will disclose. Possible risks of experimental
treatment include:

Side effects, both known and unknown
Study procedures
Treatment ineffectiveness
Treatment is not practical for all patients

Some clinical studies give patients a placebo instead of experimental treatment. Along with the risks
above, the study may need time and attention from participants, including trips to the research location,
more treatments, hospital stays, or complex dosage requirements.

Is there any cost to me or my insurance company to participate?

Participating in a legitimate clinical study is free, and clinical studies do not require you to have health insurance in order to take part. While every effort is made to ensure that study-related costs are covered by the sponsor, unforeseen expenses may arise. For instance, if you experience side effects that require medical attention outside the study protocol, these costs may not be covered by the study. You are encouraged to discuss any questions or concerns with your health insurance provider and the research team before enrolling in the study

Do I get compensated if I participate in a clinical study?

Individuals who participate in clinical studies may receive compensation for their involvement. Compensation is provided for the time and effort outlined in the informed consent form, and the amounts can vary based on study length, required procedures, and participant needs. The sponsor sets the compensation amounts. Studies may also offer free medical checks, laboratory tests, and study medications. The current compensation system is not intended to incentivize taking personal risks, and any pressure to participate for payment is against ethical standards. Before enrolling in a study, the research site will disclose the compensation available for time and travel. Compensation should never be the main reason for participation; the primary goal should be helping to advance medical research.

What should I consider before enrolling in a research study?

All potential volunteers should learn as much as possible about their disease and the clinical study they are considering. Participants are encouraged to ask questions of the research staff about the study, the care they can expect while participating, and the potential risks.

The following questions may be helpful to discuss with the research team before enrolling:

What is the purpose of the study?
Why do the researchers believe the experimental treatment will be effective?
Has the treatment been tested previously?
What types of tests and experimental therapies will be used?
How do the study’s potential risks, side effects, and benefits compare to my current treatment?
How will my illness and the effectiveness of the treatment be tracked during the study?
How will this study affect my daily life?
How long will the study last?
Who will pay for the experimental treatment and other study-related costs?
Will I be compensated for my time, travel, or any additional expenses?
Will I receive the study results, and if so, when?
Who will be responsible for my healthcare during the study?
Whom should I contact on the study team if I have questions or concerns during participation?