As a Research Participant...

Participation in any clinical study is completely voluntary. You may choose not to participate or withdraw at any time, for any reason, without penalty or loss of medical care. You are always in control of your decision.

Before joining a study, you will receive clear, detailed information about the purpose, procedures, potential risks, and possible benefits. You will only participate after you fully understand the study and provide your written consent. 

Your personal and medical information is kept confidential and handled in accordance with federal privacy laws, including HIPAA. Data collected during the study is securely stored and shared only with authorized research partners when required. 

Your health and well-being are our top priority throughout the study. Participants are closely monitored by qualified medical professionals, and any concerns or side effects are addressed promptly. 

All studies are reviewed and approved by an Institutional Review Board (IRB) to ensure participant safety, ethical conduct, and regulatory compliance. This independent oversight helps protect your rights at every stage of the research process. 

You will have access to the study team to discuss symptoms, concerns, or questions at any time during participation. In case of urgent medical issues, appropriate care and guidance will be provided immediately.