For Patients

Everything you need to know about participating in a clinical trial at ICR — the benefits, the process, and what to expect every step of the way.

Benefits of Participating

Access to New Treatments

Gain access to investigational therapies and cutting-edge treatments that may not yet be available to the public.

Compensation for Time & Travel

Participants are compensated for their time and travel at every visit. You will know the details before you sign anything.

No-Cost Study-Related Care

All exams, lab work, procedures, and study treatments are provided at no cost. No insurance needed — ever.

Personal Medical Attention

Receive dedicated, one-on-one attention from our experienced team of physicians and research coordinators.

What to Expect at ICR

01

First Contact

You reach out by phone, email, or our contact form. We listen to your questions and help you understand what studies might be a fit.

02

Pre-Screening Call

A confidential 15–20 minute conversation where we review your medical history and current health to determine preliminary eligibility.

03

Informed Consent

Before anything happens, we walk you through the full study — risks, benefits, timeline, procedures. You sign only when you are fully comfortable.

04

Screening Visit

You come into our Tampa facility for a physical exam, blood work, and any study-specific tests to confirm you qualify.

05

Study Participation

You attend regular visits over the study period. Each visit includes health monitoring, the study treatment, and time with our medical team.

06

Study Completion

After your final visit, we conduct a follow-up assessment and provide a summary of your experience. You are compensated for your time.

Risks to Be Aware Of

We believe in full transparency. Every study has potential risks, and you deserve to understand them before making a decision.

Side Effects

Investigational treatments may cause side effects, some of which may be unexpected. You will be closely monitored by our medical team at every visit, and any side effects are documented and addressed promptly.

More Visits Than Standard Care

Clinical trials typically require more frequent visits and procedures than routine medical care. The full schedule is explained during informed consent so you can decide if it fits your life.

Possibility of Receiving a Placebo

Some studies use a placebo (an inactive substance) for comparison. If a study uses placebos, you may not receive the active treatment. You will always be told during consent if this applies.

Ready to get started?

Contact Us Today
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