CLINICAL TRIALS FAQs - Healix Clinical Research

CLINICAL
TRIALS FAQs

Deciding to participate in a clinical trial is an important choice that requires thorough research to feel confident about the process. At Healix Clinical Research, we understand this and are dedicated to ensuring you feel fully informed and comfortable with your decision.

Below, we’ve provided answers to common questions about clinical trials, research studies, observational studies, and more. If you don’t find the information you need, please reach out to us directly for assistance.

Frequently Asked Questions

What is a clinical trial?

Clinical trials are designed to test and study the safety and effectiveness of investigational medications or treatments. Medications and treatments can include a drug or device that may prevent disease, become a new treatment, review existing treatments, test different dosages, other interventions, and more.

What clinical trials are available right now?

If you’re interested in learning more about the available clinical trials, head over to our trial finder. Alternatively, you can search by indication to find the right clinical trial for your condition.

Are clinical trials safe?

Our top priority is the safety of all our trial participants, and as such, we maintain close supervision by medical professionals throughout the entirety of the study. However, some participants may experience an adverse reaction to the drug or therapy being examined, potentially requiring hospitalization or other medical intervention. There is also the risk of experiencing side effects, which can range from mild to severe.

Alternatively, there are many benefits to participating in clinical trials, such as:

Improvement of your medical condition through access to new treatments
No-cost medical care and attention by highly trained research staff and medical professionals
Potential compensation for participation in the study

What is meant by informed consent?

Informed consent is a process by which clinical trial participants are given information about the research study they’re interested in to help them determine if it is the right study. Informed consent information may include criteria regarding the potential risks and benefits of the drug or device, any required medical or surgical procedures, genetic testing, medical product, study protocol, and more.

Why are clinical trials important?

Clinical trials are an essential part of making sure the drugs and medical treatments we all use are safe and effective when compared to placebo or existing therapies. We conduct trials with different populations and groups to predict how well a medication or therapy will perform in the general population when used to treat a certain condition.

Drugs and therapeutic treatments cannot be released for public consumption without FDA approval. Trial results from our research studies help to demonstrate the safety and efficacy of new drugs and devices to the FDA.

How can I qualify to participate in a clinical trial?

Not everyone who wants to participate in each clinical trial will qualify, so it’s important to closely review the qualifications. There are often extremely specific criteria for meeting the qualifications of a clinical trial.

Our research staff will ask a series of questions in a pre-screening interview, and sometimes a second screening will be required to ensure you meet all the qualifications for the trial.

If you aren’t accepted into one clinical trial, we encourage you to apply again. We consistently have a wide variety of clinical research studies at any given time.

Is health insurance required to participate in a clinical study?

No, health insurance isn’t a requirement to participate in a clinical trial. Our clinical trials have nothing to do with insurance, either private or government-provided. As a study participant, you’ll receive study-related medical examinations and investigational medication at no cost to you. Eligible participants may also receive compensation for their time and travel related to the clinical trial.

What are my rights as a clinical study participant?

As a research participant, you have the right to accurate and timely information about the study, including the inclusion criteria and exclusion criteria, the protocol, and processes. As a research participant in a clinical trial, you also have the right to ask questions at any time and have those questions promptly answered. Additionally, if you are concerned about your clinical trial participation, you have the right to withdraw at any time.

What is a study protocol in a clinical trial?

A study protocol for a clinical trial is a document that outlines how the trial will conduct research throughout the study. This document typically includes the clinical trial process, the objectives of the clinical trial, its design, methodology, and organization. The research team clearly outlines the protocol for the trial to ensure the integrity of the study and safety of the clinical trial participants. Typically, the protocol will also outline any possible risks, inclusion and exclusion criteria, details for the informed consent document, and other details pertinent to the study.

What is your privacy policy?

Healix Clinical Research will never share or sell your personally identifiable information (PII) with any company or organization. From the time of your entrance into a clinical trial, you will only be identified by initials and a unique number to parties outside of Healix Clinical Research that are participating in the conduct of the study. To learn more about the lengths we take to protect the privacy of our volunteers, visit our Privacy Policy page.

Find a Clinical Trial for Your Condition

At Healix Clinical Research, we are committed to delivering top-tier research studies to national institutions, empowering them to make informed decisions about the future of healthcare. Our studies focus on gathering critical preliminary data across various healthcare protocols, including experimental drug trials and cancer research.

Whether you are a patient, a caregiver, or a provider, we can pair you with a clinical trial or study that makes sense for your condition. Review the available clinical trials by indication and sign up to be a volunteer today.