How Clinical Trial Works

Why Participate in a Clinical Trial?

Clinical trials evaluate new investigational medications, therapies, medical devices, and disease management approaches. By participating, you contribute to medical advancements while potentially benefiting from innovative treatments. These studies play a crucial role in improving healthcare outcomes and discovering better preventive measures.

How Clinical Trial Works

01 Pre-screening

Once a participant expresses interest, the research study staff or medical professionals leading the study will call to discuss the details to determine the level of interest from the interested party. If the level of interest remains after the pre-screening, a screening appointment will be scheduled.

You’ll need a few things to apply

02 Screening Appointment

During the screening appointment, the medical professional or research study staff discuss in detail the protocols, procedures, treatments, risks, benefits, medical history, current medications, any other significant health concerns, and more criteria about the research study to ensure the participant is the right fit to volunteer for the trial.

We schedule your appointment

03 Confirmation Call

Following the screening tests, the medical professionals leading the clinical trial will review and ascertain each participant’s candidacy based on their provided screenings. The study coordinator will then call and inform you of the decision. If it is determined that you don’t qualify for the study, we encourage you to apply for future studies. You never know which study will be the right fit!

Verify qualification for study

04 Baseline Visit

At this visit, the study drug is typically dispensed, along with instructions for dosage, documentation of dosing, and other instructions pertaining to the study protocol. The study coordinator will also establish your visit schedule for the course of the study so you’ll know when to return to the office for further check-ins.

This is your first official study visit

05 Clinic Study Visits

Visits are typically more frequent during the beginning of the study. As the study progresses, they become less frequent. Each visit will require you to bring your study medication and any diaries you may have been asked to complete. The coordinator will count your medication and dispense enough to last you through the next visit.

Your safety is always our primary concern

Clinical trials vary in length, with some lasting only a few weeks or months, while others may last a few years.
The length of your study will determine the number of visits you’ll have throughout the course.
Follow-up visits are usually every three to six months for long-term studies.
Labs or other procedures

06 End Of Study

Exams and tests during this visit are similar to the one completed during the screening appointment. In order to continue your follow-up care, the coordinator will schedule a regular office visit with your physical in the next few months, aligned with your typical treatment schedule.

Your study coordinator and/or doctor will give you more information at your screening visit regarding the approximate length of each study visit.

We’ll coordinate with your physician

What to Expect from Your Participation

Participating in a clinical study can be a rewarding and enriching experience. As a participant, you will have the opportunity to contribute to the advancement of medical knowledge and potentially gain access to cutting-edge treatments. Here’s what you can expect from your participation:

Informed Consent Process

Our staff will guide you through a thorough informed consent process, explaining the study intervention, potential risks, and benefits. We will ensure all your questions are answered, so you feel fully informed before participating.

Comprehensive Medical Evaluation

You will undergo a detailed medical evaluation, including a physical exam, medical history review, and laboratory tests, to ensure you meet the study’s inclusion and exclusion criteria.

Study Intervention

Depending on the clinical study, you may receive a new medication, medical device, or behavioral health intervention. Our trained staff will administer the intervention and monitor your progress closely.

Regular Follow-Up Visits

Throughout the study, you will have regular follow-up visits where our staff will monitor your health, address any concerns, and provide ongoing support and guidance.

Compensation

We offer compensation for your time and travel, as well as any other expenses related to your participation in the study.

We are committed to ensuring that every participant has a positive and rewarding experience. Our staff is dedicated to providing exceptional care and support, and we are always available to answer any questions or concerns you may have. By participating in a clinical study, you are not only gaining access to potential new treatments but also playing a crucial role in advancing medical research and improving patient care for future generations.