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Behind the Scenes: What to Expect in a Clinical Trial

Segal Trials

So now you have decided to enroll in a clinical study, what's next?

Deciding to volunteer for a clinical trial is an important decision with potential implications for your health and the advancement of medical science. By participating, you contribute to research that may benefit many others in the future. If you're considering this step, it's essential to be well-informed about the process, potential risks, and benefits. This article provides a comprehensive overview of what to expect as a first-time clinical trial volunteer, from preparation to participation. Whether motivated by personal health reasons or a desire to contribute to scientific progress, here are the key insights and guidelines you should be aware of.

PARTICIPATING IN A STUDY IS EASY!
This Is How It Works
Decentralized Trials

1 Get Screened

Joining is Easy! Start by reaching out to us for current research opportunities. We’ll then conduct a brief assessment by asking a few pertinent questions. If, your interests and criteria align with a particular study, you’ll move on to the next step.

Patient-centricity

2 Physical Assessment

Check-Up Time! Next, you’ll visit our research facility for a complimentary physical assessment, which is required to continue. During this visit, you can ask any questions or talk about anything you’re wondering about.

Wearable Devices

3 Start Participating

Jump In and Get Started! Once you’re considered eligible to participate and you’ve reviewed and are comfortable with the study’s specifics, you’re all set to start the research process.

 

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A Clinical Study Journey Explained

For those interested in participating, here’s a comprehensive roadmap to ensure a smooth and informed experience from start to finish.

1 Pre-Screening

At this initial phase, we address specific inclusion and exclusion criteria for the study and other issues for suitability. An over the phone interview to qualify may also be required.

 2 Screening

Here’s what happens next. You will receive a study consent form (ICF) and meet the doctors and clinical coordinator. Many studies require a physical assessment and review of your medical history. Sometimes, a waiting period is required.

3 Enrollment/Randomization

Once you’re officially on board and qualified, the study will begin. You will be allocated at random to receive one of several clinical interventions, which could be a placebo. You and your Doctor will not know what you receive.

 4 Study Period

During the study period, the clinical team will monitor your progress and assess for adverse events. Depending on the study, follow up visits, labs and EKGs may be required or needed.

 5 Final Phase/End of Study

After the study journey concludes, you will have one last required safety visit with labs, physical assessments, and enclosing adverse events. Your safety and understanding are our top priority throughout this journey.

Help In Advancing Medicine

Potential Benefits of Participating

  • First access to promising care options. By participating, you could benefit from care methods that might be more effective than current standard practices.

  • Cutting-edge advantage. Secure early access to potential short-term care solutions before they become mainstream.

  • Community contribution. Your participation directly benefits society by advancing medical research and knowledge.

  • Complimentary transportation. We prioritize your convenience. Most participants receive free pick-ups and drop-offs.

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