For Patients

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Help Improve the Lives of Others

Study participation is the first step to bringing helpful new treatments to market.

What is clinical research?

Clinical research involves people from all backgrounds participating in trials to test the effectiveness of a new drug or combination of drugs, a new prevention strategy, or new ways to use existing treatments.

Clinical research allows doctors from various disciplines to evaluate new treatments, how best to apply recent developments in medicine, and ensure that patients can receive the best care options available. Some people with an illness or disease participate because they may receive the newest treatment before it’s widely available.

All participants may receive additional care and attention from the clinical research staff, study tests at no cost, and reimbursement for their time and travel. No insurance is required.

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We’re Here

We provide health education and clinical research options to a large, diverse patient population in all major therapeutic areas.

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We Care

We take pride in providing research services that are inclusive, impactful, and outstanding.

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We’re Experts

Our certified research professionals are committed to conducting all research activities with patient safety and data integrity front of mind.

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What should I know before I volunteer?

  • Clinical trials are carried out in a step-by-step process to ensure that each participant receives careful medical attention from beginning to end.
  • We understand and recognize that all participants in medical studies are volunteers; therefore, we respect every participant’s time and commitment.
  • Participation is always voluntary, and participants can choose to withdraw from a study at any time.
  • There are rigorous patient safety guidelines and operational oversight.

What are the benefits?

Take a more active role in your health care

  • You’ll have access to medical staff with frequent health check-ups throughout a study.
  • You may be given new medications or have access to devices or procedures before they are widely available.
  • You will learn more about what health resources are available to you, such as support groups and educational literature.

 

No-cost alternative option

  • You may receive tests, such as lab work, for free.
  • Most studies offer compensation for time and travel.
  • No insurance is required.
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Free Health Screenings

  • Health screenings are tests that help identify diseases before showing symptoms and may be used to determine the right study for you.
  • Which tests you need depends on your age, family history, and whether you have risk factors for certain diseases.
  • These are by appointment only and are provided at no cost to you or your insurance.
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Blood Glucose

Can help determine if you have high or low blood sugar levels. Having high or low blood sugar can lead to major health problems if not treated.

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Blood Pressure

Measures high blood pressure (hypertension) and low blood pressure (hypotension) which can be an indicator of health conditions, including heart disease.

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Pulmonary Screening

Measures lung volume, capacity, rates of flow, and gas exchange, which can be used to evaluate a broad range of lung diseases including asthma or emphysema.

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Depression Screening

 Questionnaire used to assess if you are suffering from depression. Untreated depression can lead to overwhelming sadness, loss of appetite, and thoughts of suicide.

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Memory Screening

Composed of a series of questions and/or tasks that are designed to test memory, language skills, and other mental functions. Changes to your memory may indicate an underlying issue that may need attention.

Frequently Asked Questions

What is informed consent?

An informed consent is a documented process of communication between the research participant and the health care provider to outline an agreement or permission for care, treatment, or services and serves to protect the rights and well-being of all research participants.

What does eligibility criteria mean?

Requirements that must be met for a person to be included in a clinical trial. These can include specific factors such as age, aspects of general health, or a history of previous treatment.

How many visits are required?

It depends on the study, but there are three types of visits that happen during a clinical trial.

  • Screening visit: Informed consent and a complete medical history
  • Baseline visit: Receive your first study medication or receive your first treatment
  • Routine study visits: Regularly scheduled check-up visits throughout the length of the study to track the progress of the medication or treatment

What happens with my data?

All information collected is kept private and confidential, with data reports, sharing, and storage done in a HIPAA manner. Data is analyzed by physicians and findings are reported to the FDA (Food and Drug Administration) for their consideration in the approval of new medications or devices.

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