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Rocket trials

Connecting You To Clinical Trials

Sign up to be considered for current and future studies. If there is no active study currently enrolling for the indication you select, we will place your information in our database and contact you if a new study opens up.

Enter your information to join!

Why Participate?

  • Everyone has a different reason for participating in a clinical trial. The most common reasons include:
  • No-cost study-related care from a local physician and/or specialist
  • No insurance required to participate
  • Compensation for your time and travel
  • Chance to help advance medical research
  • Access to the latest treatment options

LOCATION: Various

Enter your information on the form or contact our research staff today.

1-000-00-0000

Hours of Operation
Monday – Friday: 8:00 AM – 5PM
Saturday & Sunday: Closed

About Rocket Clinical

Rocket Clinical aims to connect people to clinical research studies in their area. We have access to hundreds of studies across the nation every year and carefully match people to the studies best for them. Through investigating the effectiveness of new treatments for diseases, these studies help advance healthcare.

Feel free to explore our website to learn more about clinical research or find studies that you can participate in.

What’s Involved?

1 - SIGN UP

Fill out the form at the top of the webpage. Signing up does not guarantee that you will participate in the study.

2 - PHONE CALL / TEXT

The study team reviews
your information. If the study might be a good fit, someone will contact you for further information or to schedule a screening visit.

3 - SCREENING VISIT

The research site will assess if you are fully qualified to participate in the study. All of the study details will be explained to you at this time.

4 - STUDY PARTICIPATON

Fully qualified participants may be offered the chance to enroll and receive the study treatment over the course of the study.

FAQs

What is a clinical research study?

A clinical research study (also known as a clinical trial) is a medical research project conducted to find better ways to prevent, screen for, diagnose, or treat disease. To do so, the study team investigates the effectiveness of new medications and treatments by enrolling human volunteers. These studies follow strict, scientific standards which protect patients and help produce reliable clinical trial results. Therefore, all participants are under the supervision of a doctor and/or health professionals throughout the entirety of the study. Clinical trials are one of the final stages of a long and careful research and development process. As the trial goes on, more and more information is gathered about the treatment or device under investigation. The overall goal of a trial is to improve healthcare and the treatments available to the general public.

What are the benefits of participating in a clinical trial?

Clinical trials help advance medical research and improve healthcare. By participating in a clinical trial, you have the opportunity to gain access to the latest treatment options from quality health professionals. In addition, many trials offer: No-cost study-related care from a local physician and/or specialist No insurance required to participate Compensation for your time and travel

What if I don’t qualify for the clinical trial I’m interested in?

Each study follows a specific set of guidelines that describes who is eligible to participate. Common eligibility criteria may include: age group, medical history, current health status, past medical treatments, and whether or not you have a particular disease. If you do not qualify for the study you are interested in, there may be another study currently enrolling in your area. You can search for additional trials on our website or sign up to be notified when we match you to a new study.

What if I change my mind about participating after the study starts?

The study team will try their best to work with you to make accommodations so you can participate. However, we understand that circumstances change, so you are always able to stop your participation. Please reach out to the study team if this occurs.

How much time is required to participate in a study?

The time commitment required varies for every study. Some studies involve weekly office visits, while other’s require overnight stays at the clinic. Overall the study can last a few weeks to several months. When possible we try to list the time requirement on our sign up forms. However, if you still have questions the study team will go over all of the requirements with you during your screening visit before you are enrolled in the study.

Will I receive a placebo?

A placebo is a medication that does not contain the study drug which some studies use to compare against the study treatment. Not all trials use placebos. Oftentimes, the study treatment will be compared against the current standard medication or older treatments. Regardless of which medication you receive, you will still have access to the health professionals assigned to your study. Before you are enrolled in a trial, the study team will go over which options are used in each trial.

Will I be able to continue taking the study drug after completion of the study?

Whether or not you will be able to continue taking the study treatment after your participation has ended, varies for each study. You can talk to the study team about whether this is an option for your study before enrollment.

What do “phases” of a clinical trial mean?

You may have heard of clinical trials and the “phases” associated with them. There are 5 phases, which are defined by the FDA (U.S. Food and Drug Administration). The three most common phases you may encounter are described below. Phase I studies are done during the earliest part of researching a treatment. These trials are usually small and include healthy volunteers to find out the safety of the drug. Phase II studies gather information to find out if the drug will have an impact on a certain condition. These studies typically use larger groups of volunteers to determine treatment effectiveness. Phase III studies look further into safety and effectiveness of the drugs while comparing to existing treatments or a placebo. These studies also use larger groups of volunteers.

PRIVACY POLICY AGREEMENT

Who we are

Rocket Clinical (a part of Rocket Trials, LLC) seeks to connect you to local clinical trials and study clinics. You may have arrived at this site because you were looking for clinical trial opportunities to participate in studies that investigate the latest medical treatments or because you clicked on an ad for a currently running clinical trial. The following information describes how we collect, use, and store your information.

What Information We Collect

You may have been asked to fill out a form for a potential study opportunity. Filling out the form and submitting your information is completely optional. Typically, this information constitutes your name, email, phone number, date of birth, and zip code.

How We Use Your Data

The information you provide is used to contact you in regards to your interest in participating in a clinical trial. Any basic contact information you provide may also be used during pre-screening in order to determine if the study you signed up for would be a good fit. Each study has predetermined criteria that must be met in order to participate. By submitting your information, you are not officially enrolling in a study.

Your information may also be shared with our partner clinics who are in charge of the clinical trial so that they may respond to your interest. They will only use your information for study related purposes unless you have given further consent.

Third Parties

We will not disclose, sell, or distribute your information to any third parties without your prior agreement unless required to do so by law.

Once you are officially enrolled in a clinical trial with one of our partner clinics, you will be subject to the privacy policy they have in place for that particular study. However, you will be given the opportunity to provide your consent before this takes place.

Security

All information is stored in our HIPAA-compliant study portal that can only be accessed by staff members and clinic physicians. We are the sole owner of this portal and only allow partner access to our partner clinics and clients. We have implemented and will maintain all necessary technical, organizational, and physical security measures that are reasonable and designed to help protect your information from unauthorized access, disclosure, alteration, or destruction.

Consent

By signing up, you agree to receive text messages, emails, or phone calls about this and similar studies near you. Text message and data rates may apply. You have the option to unsubscribe or opt out of any future communications about clinical trials if you so choose. To do so please, reach out to us to express your request that we cease communications.

By filling out the form, you state that you are the person whose name is listed on the form and that all information provided is current and correct to the best of your knowledge. If you are the parent or legal caretaker of the person interested in this trial you may enter their health information in their place and/ or your contact information.