Participants
We value Patients as Partners.
Join a Trial Today
$200 per visit + $300 dosing day
Major Depressive Disorder
26-MDD-10
18 to 70 years
52 weeks
Outpatient
Inpatient & Outpatient $200 per night
Schizophrenia
26-SCZ-07
Ages 18–65
18 weeks
Outpatient
How to Enroll in a Trial
By participating in any study, you are contributing to the advancement of new medications aimed at improving the treatment of mental illness.
Phone Screen
You can get in touch with our research coordinators at 314-282-3521 to complete a quick phone conversation to help determine if one of our current studies is a good fit for you.
On-Site Pre-Screen
You will meet with one of our research coordinators, who will recommend a study that she believes best suits your psychiatric needs.
Eligibility
Once your pre-screening is complete, the eligibility process will involve further assessments and evaluations to ensure you meet all the criteria for the study.
Participate
If you choose to participate in the recommended study, then you will meet with the Study Coordinator to complete each visit in the study. For each visit you complete, you will be compensated, and all transportation will be provided if necessary.
We have a Referral Program
Frequently Asked Questions
A clinical research study involves human participants in medical investigations that offer doctors and researchers deeper insights into specific diseases, aiding in the development of new treatments and medications. These studies are generally classified into two main types: observational and interventional. Observational studies seek to uncover the root causes of diseases or conditions, whereas interventional studies assess the effectiveness of new treatments, procedures, or lifestyle changes in curing or preventing diseases.
The eligibility criteria for clinical research study participation are determined by specific inclusion and exclusion guidelines. These criteria may include having specific medical conditions, falling within certain age groups, or having particular medical histories. These requirements are set to ensure that researchers collect pertinent data while prioritizing participant safety.
When you join a clinical research study, you contribute to scientific knowledge and potentially enhance global health outcomes. Beyond advancing science, these studies often encourage participants to adopt healthier lifestyles and become more engaged in their healthcare. Participants typically receive free medical care related to the study, and in interventional studies, they may access new treatments not yet available to the general public.
The duration of every research study varies widely. Some studies may last only a few weeks, while others can span several months or even years. Longer studies often provide more valuable and comprehensive information. Our aim is to ensure that participating in the study is as convenient as possible for all selected individuals.
Payment for clinical trials can vary based on factors such as the type and frequency of assessments conducted during each visit, the duration of the trial, and any additional study requirements. Participants usually receive stipends after completing each scheduled visit, and compensation for longer trials can range from hundreds to thousands of dollars in total.
We respect the personal and private nature of psychiatric assessments and treatments. Confidentiality in our clinical trials is rigorously upheld to safeguard participants’ privacy from external entities, and we are legally obligated to protect their confidentiality. This means we do not disclose participants’ information to employers or insurance companies. However, if pertinent to the study, we may need to gather details about your primary healthcare provider, always with the participant’s signed consent beforehand.
Arch Clinical Trials has its own building for inpatient studies, located at 1400 Lemay Ferry Road. Only subjects participating in inpatient trials will be staying at this center.