Local research studies are evaluating investigational add-on treatments for adults with Parkinson’s disease. Discover if you qualify today.
About Clinical Trials
Before emerging therapies can be approved for widespread public use, they must first be tested in controlled clinical research settings to ensure that new medical treatments are safe and effective. By joining a study, participants are playing a vital role in helping doctors and scientists make meaningful progress in Parkinson’s disease research, and work towards a more hopeful future for fellow patients.
WHAT ARE THE BENEFITS?
Participants in Parkinson’s disease clinical studies will have access to specialists who understand their unique situation and can help answer questions and address concerns from participants or their loved ones. Throughout the duration of a trial, participants should expect to be monitored in a safe, professional clinical environment and have the opportunity to contribute to scientific innovation.
WHAT IS BEING TESTED?
Researchers are exploring new pathways for treatment of Parkison’s disease. Ongoing clinical trials are evaluating potential new approaches to evaluate if they can help reduce “OFF” time and improve daily motor function without worsening dyskinesia. Read our FAQs to learn more about clinical research studies for people with Parkinson’s disease, and what one might expect as a participant.
What Can I Expect?
The Process: Studies are often randomized and placebo-controlled. This means you may receive an active investigational treatment or a placebo (which contains no active treatment). This is necessary to scientifically prove if a new treatment works.
The Commitment: Research studies often require scheduled appointments at the study clinic and a commitment to your health. This may involve keeping a “motor diary” at home to track your “ON” and “OFF” times (times when Parkinson’s medication is working and times when it is not). Participants may also be asked to wear a high-tech, bracelet-like sensor on their wrist to track activity and sleep quality.
Safety First: Safety is always the top priority. Participation is entirely voluntary, and patient safety and rights are protected by an Institutional Review Board (IRB).
Clinical Trials Make A Difference
Participation in a clinical study provides valuable information to researchers that could eventually lead to additional treatments and to potential advancements in care options. Take our short survey to see if you or a loved one may be a good fit. There is no obligation to participate.
From the Community
“There are clinical trials out there. I don’t want to just sit here and let it overtake me, I want to feel like I’m battling back, even just a little bit.”Todd, FL
“If I have the opportunity to help myself and help other people who are dealing with my condition, if that’s the way I can contribute, sign me up.”Elizabeth, VA
“Without the first person with the first step, you never know what greater good could come.”Thomas, MD
“If you’re not doing clinical trials, you’re not making progress. The more people examining it and studying it, the better.”JENNIFER, AUS
Still Have Questions?
Contact us anytime at help@clinicalenrollment.com.