Once... as recently as 20 years ago, it was not uncommon for patients with arthritis to rapidly become crippled or to die from the devastating effects of arthritis.
Today, many patients are able to experience remission from their arthritis. To get to this point has taken the work of many hard-working researchers as well as the dedication of thousands of patient volunteers.
The Benefits of Exercise::
How Often Should I Exercise? Ask your doctor or physical therapist for recommendations specific Most people with arthritis CAN participate in exercise.
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The goal of arthritis clinical research is to safely translate promising basic laboratory discoveries into safe and effective medical practice.
All clinical research conducted in the United States is guided by the Nuremberg code. These guiding principles were established to protect human subjects from unethical conduct, such as what took place under the Nazis during World War II.
The eight fundamental standards that guide clinical research are:
The risks of a study must be minimized through sound research design and methodology
Clinical Trials Forums, Discussions, egroups, Listserves, and ::
Inadequate research, a lack of evidence-based treatment, and a remarkable shortage of clinical trials has prevented the advancement of disease-specific
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The Herbal Insider Vol 1, Issue 1::
What I do know is that if I exercise enough growing my red beans and picking my .. (German clinical trials have already shown it to be as effective and
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Risks must be reasonable relative to the anticipated benefits of the study
The selection of research volunteers must be equitable and without bias
Informed consent must be obtained from the person participating in the study
Member Story - Taking Control::
The extreme diet I was on before joining the clinical trial was a concern to my new doctor. He told me I was losing fat to a risky point and told me to gain
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The consent language agreed to and the process for obtaining consent must be documented carefully
Research patient privacy and confidentiality must be protected
Ongoing safety of research volunteers must be adequately monitored
Vulnerable patients such as children must be adequately protected
All clinical trials in the United States are overseen by what is called an Institutional Review Board (IRB). This is a panel of people with diverse backgrounds who are unaffiliated with the center conducting the research. While there are many IRBs in the United States, they all have a common goal.
The goal of the IRB is to safeguard the privacy, welfare, and rights of volunteers participating in clinical research. The IRB may approve, disapprove, modify, or suspend research. The IRB has final authority with regard to human research.
The informed consent process is critical to the ethical and safe conduct of a clinical trial. During the process of informed consent, it is important that the prospective volunteer have time to read and understand the consent form and have all questions answered by professionals conducting the study. The consent form must contain sufficient information about the research as well as the risks and benefits so that the volunteer can make an informed decision about participation.
Consent forms should:
Describe the study as fully as possible
Point out foreseeable risks or discomforts
Explain anticipated benefits
Explain alternatives
Describe how confidentiality will be maintained
Describe compensation, if any
Provide contacts who will provide more information or discuss concerns
Explain that participation is voluntary and the volunteer may withdraw at any time
The Health Insurance Portability and Accountability Act (HIPAA) was established in 2003 to protect the privacy on health information. Centers conducting clinical research must adhere to HIPAA regulations when it comes to disclosing confidential patient information.
All arthritis research conducted at the Arthritis and Osteoporosis Center of Maryland (AOC) supports and follows the above principles. Any questions should be directed to the principal Investigator, Dr. Nathan Wei.
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My Doctor Has Asked Me To Participate In An Arthritis Clinical Research Trial... What Should I Know?