FAQs & Resources

Frequently Asked Questions

What is a clinical study?

A clinical study, also known as a clinical trial, is designed to learn if an investigational drug is safe and effective for public use. Participants are given specific medical treatments and researchers closely monitor the results to help decide if the drug should be approved for wider distribution. All medications on the market today have gone through this process.

What are my responsibilities while participating in the study?

If you choose to participate in the study, you will be provided with guidelines and instructions to ensure your safety and well-being. You will be required to share information about your current and past health to protect your safety throughout the study. Additionally, it is advisable to inform your primary care physician about your involvement in the study for comprehensive care and support.

Is participation voluntary?

Yes, participation in the study is entirely voluntary. You have the right to withdraw at any time for any reason. If you decide to leave the study, you will not be charged, nor will you lose any benefits you are otherwise entitled to.

Are there costs or compensation involved in participating in this study?

It will not cost you anything to take part in this study. You can be compensated $575 or more in each study group.

How many posttraumatic stress disorder (PTSD) treatment options are FDA approved?

Despite the significant impact of PTSD on patients’ daily lives, PTSD treatment options are limited. Currently, there are only two FDA-approved medications for PTSD, both of which are used to treat depression, and none have been approved since 2001.

How many veterans have PTSD?

Posttraumatic stress disorder (PTSD) is a significant concern for US combat veterans, with an estimated 7% of veterans affected at some point in their lifetime. This rate varies depending on factors like the era of service, branch, and deployment status.

https://www.ptsd.va.gov/understand/common/common_veterans.asp