Finding a Study That’s Right For You
If you are thinking about participating in a clinical trial you will be connected with a member of our research team. Specific studies require specific criteria. Before you start on a trial, you will go through a screening and consent process. This is how Dr. Carlson and his team can ensure participants meet safety criteria for the study drug or device that is being developed. It is also an opportunity for you to ask questions and make sure you feel the study is the right fit for you. You may be compensated in consideration of your time and travel.
No Overnight Stays Required for Our Studies
More Details about the Screening and Consent Process
We’ll begin with a phone Q&A about your health and medical history. At that time we’ll schedule an appointment with the doctor to learn more about the study.
Informed Consent: At your first appointment, the study team will review the details of the study, including possible risks and benefits, so you will know what to expect. If you decide to participate, you will give written permission for additional screening and access to your health records.
Screening Visit: This visit will confirm that you meet study participation requirements. It includes a more detailed review of your medical history, a physical exam and may also include additional tests related to your condition.
What to Expect After Consenting to Participate in a Study
Taking part in a research study is different from regular medical care. When in a clinical trial, you will primarily interact with the Be Well Clinical Studies team. Our team includes study nurses, coordinators and research staff who work closely with Dr. Carlson and Be Well MD. Before you consent to participate, you will be told how the study works.
You may have additional scheduled visits and procedures, extra laboratory tests, and/or follow a modified treatment plan.
You can stop participating at any time—the decision to stop will not affect your regular medical care or any benefits to which you are entitled.
Where permissible, reimbursement for study-related expenses—such as parking and travel—may be provided.
To research a study drug for effectiveness and safety, some participants are given the study drug and others are given standard of care or a placebo.