Are Clinical Trials for You?
- Participants must meet stringent criteria (medication, lifestyle choices, stage of disease, etc.) to be an eligible candidate for a clinical research trial.
- Participation generally includes multiple office visits and additional time requirements from the participant.
- Some potential participants are uneasy about anything that is “investigational”. The informed consent provides information on known and potential risks and benefits to participating in the trial.
Why Should I Participate?
- Study related evaluations (performed by licensed, board certified practitioners), medications and procedures are provided at no charge to the participant or their insurers.
- Participants are excited to be part of advancing modern medicine and devices. There is always a risk associated with medications but after reviewing the information in the informed consent form (ICF) and discussing the potential benefits, they can make a decision to proceed with their enrollment into the study.
- Participants have the opportunity to improve the livelihood of others, and aid in new scientific discoveries allowing for advancements in available health care and treatment options.
- There are many reason’s clinical trials are conducted but it is important to ensure the safety and efficacy of new or improved medications and devices. Without participant’s, we would not know whether a medication, vaccine or device is effective and safe with the benefits outweighing the risk.
- Not all studies are related only to medications or vaccines. There are also trials conducted for devices that may be new to the market or that have undergone improvements.
- We greatly appreciate our participants and their contributions to furthering research; allowing new medications, devices and vaccines to become available.
- You will be provided with an Informed Consent Form (ICF) before we collect any data. This form has been reviewed and approved by an Independent Ethics Committee (IEC) or Independent Review Board (IRB) that is overseen by the Food and Drug Administration (FDA).
- The risks and benefits of participating in a trial vary widely between each trial and cannot be generally summarized. If you enroll into a trial, you will be informed of any changes to the risks and benefits as they become available; as required by law. The Principle Investigators and ASR staff will always be available to answer any questions you may have. We encourage you to ask questions at any time.
- You will never be pressured to enroll in a study. Your decision to participate is entirely voluntary and at any time you can choose to withdraw your consent.
- You can take as much time as needed to discuss the study with your family or Primary Care Provider before participating.
- Your information will be kept confidential. ASR is a HIPAA covered entity and complies with all local, state, and federal regulations. We will tell you what we are going to do with your information. If you no longer want us to use your information, simply let us know.
Compensation
- Participant’s may receive compensation for their time and travel. The total compensation depends on each study but may range from $25 – $150 per visit. It is important to note that the amount is relative to the requirements of the participant and is in no way related to the risk of participation.
- Compensation is generally provided in the form of a check unless specified otherwise, after completing study “milestones”. The amount you are compensated and when you will receive compensation is explained in the Informed Consent Form (ICF).
- Most clinical trials last from 6 months to 2 years, depending on the study. During this time, all study related activities as explained in the ICF (examinations, lab work, EKG’s, lung function tests, X-rays, study related medications, etc.) are provided at no charge to the participant.
Would You Like to Participate in One of the Following Trials We Have to Offer?
Locations, Contact Information, and Hours of Operation
Hours of Operation
Monday through Thursday
8:00 a.m. to 5:00 p.m.
Friday
Closed
Location
Address:
200 N 3rd St Suite 110
Boise, ID 83702
Office Number:
+1(208)-906-1600