FAQs
CLINICAL RESEARCH FAQs
Clinical research is one of the main ways we move forward in our understanding of medical conditions and implementation of new drugs. All types of people are needed for research, from those who have been diagnosed with specific diseases to those who are completely healthy. All volunteers receive detailed information regarding the risks and benefits of participation in each study. We welcome all questions and concerns you may have as it is important to us that you are comfortable and aware of all aspects involved with being a research volunteer. You always maintain the option of discontinuing your participation at any time.
What is a clinical trial?
A clinical trial is a carefully designed study that involves people like you who volunteer to receive investigational treatments under close supervision of a physician and other research professionals. All clinical trials are independently reviewed by Institutional Review Boards (IRBs) which are independent committees who ensure your rights are fully protected and that you are not exposed to any unnecessary risks.
Why is clinical research important?
Clinical research is important in order to develop new therapies and diagnostic procedures as well as to understand how diseases develop. Observational studies may help identify risk factors for the development of a particular disease, such as the association between smoking and lung cancer. Outcomes-based research can help doctors identify the most effective therapies and treatments for a number of conditions. Another aspect of clinical research is the development of new technologies for use in health care, ranging from surgical tools and materials to hearing aids and artificial limbs.
Does it cost anything to participate?/Will I be paid to participate in the study?
All participants in a clinical trial are volunteers and do not pay to take part in the study. Qualified participants will receive all investigational medication and study related medical exams at no cost, and you may also receive compensation for time and travel.
What are the pros and cons of participating in a clinical trial?
The benefits of clinical trials are many and range from taking an active role in the management of one’s own health care, helping others by aiding the process of knowledge acquisition and development of enhanced treatments, being cared for by leading health-care teams in a given field, and in some cases, receiving access to new treatments before they are approved. However, there are also risks, including side effects of drugs and risks of any procedures that may be performed. In some cases, clinical-trial participation may require more frequent doctor visits or hospitalizations than standard care, and you may have to travel to a study site that is farther away than your local health-care practitioner’s office.
I’m interested! What’s next?
Contact Pivotal Clinical Research & Associates…
Call our office (770) 376-7912
Email our research team (research@pivotalcra.com) to ask any questions.
REFERENCES:
National Institute of Health
National Institutes of Health -Clinical Trials
Center for Information and Study on Research Participation
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