Research
Clinical Trials at Redbird Research
Clinical trials are the backbone of medical progress. On this page, you’ll learn what clinical trials are, why your potential participation in mental health clinical trials matters, how we prioritize your safety throughout the process, and find helpful resources plus answers to frequently asked questions.
clinical trials
What are Clinical Trials?
Clinical trials are research studies designed to evaluate whether new medical treatments, therapies, or devices are safe and effective. They play a crucial role in developing better solutions for a wide range of health conditions.
At Redbird Research, we are currently enrolling in clinical trials focused on psychiatric and central nervous system disorders. Through these studies, we contribute to the advancement of medical science and help shape the future of mental health care.
By joining a clinical trial, you may gain early access to innovative treatments while also supporting medical research that benefits others. Every study we conduct follows strict ethical guidelines and scientific protocols to ensure participant safety and high standards of care.
Why
Why Participate in a Clinical Trial?
- Contribute to Medical Advances
By participating in a clinical trial, you help researchers develop better treatments for mental health and other medical conditions. Your involvement plays a key role in advancing scientific understanding and improving patient care.
- Access to Innovative Therapies
Clinical trials could give you early access to investigational products that may be more effective than standard care. These therapies are not yet available to the public and might offer new hope for managing your condition.
- Close Monitoring
Participants receive regular check-ups and health evaluations throughout the study. Our experienced clinical team ensures you are safe, supported, and fully informed at every step.
- Make a Difference
By joining a clinical trial, you contribute to the future of treatment, helping others who may benefit in the future from the treatments being studied. Your participation supports future patients and helps pave the way for new therapies that could become tomorrow’s standard of care.
Safety
Your Safety is Our Priority
At Redbird Research, your safety and well-being always come first. Before enrolling in any clinical trial, you’ll receive clear, detailed information about the study’s purpose, procedures, potential risks, and benefits. Our experienced research team is here to answer your questions and guide you every step of the way, so you can make a fully informed and confident decision.
FAQ
Frequently Asked Questions
Answers to some of our most frequently asked questions
What are my responsibilities as a participant in a clinical research study?
As a participant in a clinical research study, you have several important responsibilities:
- Read the consent form thoroughly and ask the study staff any questions you may have. It’s essential that you understand what will happen during the study before agreeing to participate.
- Consider the potential benefits and risks of being in the study and discuss them with the study staff or your doctor if you have concerns.
- Follow all study instructions and any restrictions, including taking medications exactly as advised by the research staff.
- Attend all scheduled visits and be on time. Your participation and consistency are crucial to the success of the study.
- Report any issues or side effects with the study medication, procedure, or device to the study staff right away.
- Avoid pregnancy while participating in the study, either for yourself or your partner, if applicable.
- Answer all questions honestly to help ensure the study results are accurate and reliable.
- If you decide to leave the study at any time, speak with the study staff so they can guide you on the next steps.
What is a placebo?
A placebo is a substance or treatment that looks like the real treatment being studied but doesn’t contain any active ingredients. If you are receiving oral medication in a clinical trial, all pills, tablets, or capsules look the same and taste the same whether you are receiving a placebo or the research medication. Placebos are used to help researchers understand the effects of the actual treatment compared to no treatment. If you are given a placebo, it will not have any direct effect on your condition, but your participation still provides valuable information to help researchers learn more about the treatment.
Will I know if I am receiving the actual treatment or a placebo?
In many clinical trials, especially those that are double-blind, neither the participants nor the researchers know who is receiving the actual treatment and who is receiving the placebo. This method helps to prevent bias and ensure the study results are reliable. Information about what you received during the study will not be available at the time you complete the study. However, once all study participants across all centers complete the study, this information may become available.
What happens if I experience side effects during the trial?
If you experience any side effects or feel unwell during the trial, it’s important to inform the study staff immediately. You will be closely monitored, and any necessary medical care will be provided. Depending on the nature of the side effects, the study team may adjust your treatment, provide additional support, or decide to withdraw you from the trial if necessary to protect your health.
Can I leave the clinical trial if I change my mind?
Yes, you can leave the clinical trial at any time, for any reason. Your participation is completely voluntary, and you have the right to withdraw without any penalty or loss of benefits to which you are otherwise entitled. If you decide to leave, please inform the study staff so they can guide you on the process and discuss any follow-up care that may be needed.
Who oversees the safety of clinical trials?
Clinical trials are reviewed and monitored by Institutional Review Boards (IRBs), ethics committees, and government agencies like the FDA to ensure participant safety and ethical research conduct.
Will I be paid for participating in a clinical trial?
Yes, all of studies offer compensation for your time and travel. Details about compensation will be provided during the screening process so that you can make an informed decision.
How long do clinical trials usually last?
It depends on the study. Some trials last a few weeks, while others might have periodic visits over the course of several months. You’ll be informed of the exact time commitment before you decide to participate.
Will my personal and medical information be kept private?
Yes. All personal health information is kept strictly confidential and protected in compliance with HIPAA and other privacy regulations.
Resources
Learn More About Clinical Trials
To better understand clinical trials and their importance, we encourage you to explore the following resources:
- FDA Clinical Trials: Learn about clinical trial phases and how treatments are developed.
- NIH Clinical Trials and You: Find out more about how clinical trials work, why they are important, and hear from people who have participated in studies.
- NIMH Clinical Trials – Psychiatry and Mental Health: The National Institute of Mental Health provides information specific to clinical trials in psychiatry, including ongoing studies in mental health and CNS disorders.
- ClinicalTrials.gov: A comprehensive database of privately and publicly funded clinical studies conducted around the world. You can search for trials by condition, location, and other criteria.
If you have any questions or are interested in participating in one of our clinical trials, you can take a look at our current available clinical trials below or you can click here.
Clinical Research
Current Clinical Trials at Redbird Research
Redbird Research is currently enrolling participants for clinical trials focused on psychiatric and central nervous system (CNS) disorders. If you’re interested in joining a study, click on the condition that applies to you below to begin the quick pre-screening process and see if you qualify.
- Colorado
Alcohol Use Disorder
- Colorado
PTSD
- Colorado
Depression
- West Virginia
Bipolar Disorder
- Nevada
Schizophrenia
- Colorado