What is a clinical trial?
A clinical trial is a research study conducted to assess if investigational drugs, medical devices, or treatment techniques are safe and work as expected in people.
Why are clinical trials important?
Clinical trials generate the evidence needed to determine whether new medical treatments are safe and effective. Without them, many of the medicines, vaccines, and tests we rely on today wouldn’t exist.
Who can take part in a clinical trial?
Each trial has eligibility rules based on age, health, and other factors. Some trials need people with certain conditions, others involve healthy volunteers.
What should I consider before joining a clinical trial?
You should know as much as possible about the clinical trial and feel comfortable asking the healthcare team questions about it, including the care expected during the trial, the costs involved, and any other details. Some of the answers to these questions will be available in the informed consent document.
Are clinical trials a legitimate option for medical care?
Yes. In many cases, participants receive dedicated medical attention and may even have access to specialist tests and monitoring at no cost.
What happens during a clinical trial?
This depends on the study, but typically you’ll go through a screening process, receive the treatment or placebo, attend follow-up visits, and have tests to monitor your health.
How long do clinical trials last?
Trials can last from a few weeks to several years, depending on the treatment being studied and the goals of the research.
What are side effects and adverse reactions?
Side effects are any undesired actions or effects of a drug or treatment. Experimental treatments must be evaluated for both immediate and long-term side effects.
Can I keep seeing my primary healthcare provider while I’m in a trial?
Most clinical trials provide short-term treatments related to a designated illness or condition, but do not provide extended or complete primary health care so you should continue to see your main healthcare provider.
Will my privacy be protected if I take part in clinical trials?
Yes. All medical records and research materials that identify you will be confidentially held. Only individuals working on the study will have access to your personal information.
Can I leave a clinical trial after it starts?
Yes. Participation is voluntary, and you can withdraw at any time without affecting your standard medical care. If you do leave, you should let the research team know so that we may retrieve any remaining medication and do an exit visit if possible.
How do clinical trial results get used?
Results help doctors, regulators, and researchers decide whether a treatment should be approved, modified, or studied further.
What is informed consent and why does it matter?
Informed consent is the process of explaining the trial’s purpose, risks, benefits, and requirements before you decide whether to participate. It ensures your decision is voluntary and based on full understanding.
How do paid clinical trials work in the US?
Some trials offer payment for your time and participation. Others reimburse for expenses such as travel or childcare. Payment varies based on the type and length of the study.
Will I get paid for taking part in a US clinical trial?
Reimbursement may be paid for time and participation. Every study is different and full details will be provided before you decide whether to join.
Will I receive a 1099-MISC for tax filing?
A Form 1099-MISC will be issued to any patient or caregiver who has received patient stipends of $600 or more paid during the year. This is a mandatory filing for Velocity Clinical Research due to Internal Revenue Service rules and regulations. The Form 1099-MISC will be mailed no later than January 31 of the following year.
How do I join a medical research study in the US?
You can search ClinicalTrials.gov, talk to your doctor, or register your interest via our website to find nearby studies that match your health profile.
How is my safety protected in US clinical trials?
All US trials are reviewed by an Institutional Review Board (IRB) to ensure the risks are minimized and participants’ rights are protected.
