Frequently Ask Questions | Center for Family Health Research in Zambia (CFHRZ)

Frequently Asked Questions

What is a clinical research site?

What does CFHRZ stand for?

Center for Family Health Research in Zambia

How can I participate in a clinical research study at CFHRZ?

To participate in a clinical research study at CFHRZ, you would typically need to meet specific eligibility criteria set by the researchers conducting the study. You can inquire about ongoing studies and eligibility requirements by contacting CFHRZ directly.

What are the benefits of participating in a clinical research study?

Participating in a clinical research study may provide benefits such as access to potentially new and innovative treatments or interventions before they become widely available, close monitoring by healthcare professionals, and the opportunity to contribute to scientific advancements.

Are there any risks involved in participating in a clinical research study?

Yes, there can be risks involved in participating in a clinical research study. These risks vary depending on the nature of the study, the experimental interventions used, and individual factors. It is important to thoroughly understand and discuss the potential risks and benefits with the researchers before deciding to participate.

How are participants protected during a clinical research study at CFHRZ?

Participants in clinical research studies at CFHRZ are protected through a process called informed consent. This involves providing detailed information about the study, including its purpose, procedures, potential risks, and benefits. Participants have the right to ask questions, understand the information provided, and voluntarily decide whether to participate. Additionally, research studies are subject to ethical and regulatory oversight to ensure participant safety.