Participate in Clinical Research
Clinical research evaluates potential new medications, therapies, technologies, and approaches to mental health care.
Depending on the study, participants may receive an investigational treatment, another study intervention, or take part in research activities designed to better understand a condition or treatment. Participation may or may not provide a direct medical benefit. However, the information gained from clinical research may help advance the development of future treatments and improve our understanding of mental health conditions.
What is Clinical Research?
Clinical research studies evaluate potential treatments, therapies, technologies, and approaches to better understand their safety, effectiveness, and how they may affect people with specific conditions.Each study has its own eligibility requirements, procedures, potential risks, and potential benefits.
Who Can Participate?
Every clinical study has specific eligibility requirements. These factors may include:- Age
- Diagnosis or symptoms
- Previous treatment
- Current medications
- Medical or psychiatric history
- Other study-specific criteria
What to Expect
1
Connect With the Research Team
After you express interest, a member of the research team may contact you to learn more about your interest and provide additional information.
2
Complete an Initial Eligibility Review
The research team may ask you questions about your health, medical history, and other information to determine whether a study may be appropriate for you.
3
Learn About the Study
If a study looks like a potential fit, the research team will explain what the study is about and what participation involves. This includes study visits and procedures, potential risks and possible benefits, time commitment.
4
Decide Whether to Participate
Participation is voluntary. You will have the opportunity to ask questions and decide whether participation is right for you. Choosing to learn more about a study does not obligate you to participate.
Informed Consent
Before joining a clinical trial, eligible participants receive information about the study and have an opportunity to ask questions.The informed-consent process is designed to help you understand the study, including its purpose, procedures, potential risks and potential benefits, before deciding whether to participate.
Participation is voluntary, and you may choose not to participate.
Research Opportunities
Find Out About Future Research Opportunities
We are preparing new research opportunities across psychiatry and neuroscience.
Join our research interest list to receive information about opportunities that may become available in your area.
Our Commitment to Responsible Research
Patient safety, dignity, privacy, and informed decision-making are central to research conducted through PsychPlus.
Research is conducted according to applicable study protocols, informed-consent requirements, privacy protections, regulatory requirements, and Good Clinical Practice principles, with appropriate independent review as required.
Frequently Asked Questions
Interested in Clinical Research?
Tell us that you are interested in learning about research opportunities that may become available in your area.
Participate in Clinical Research
Privacy note:
Please do not include detailed medical history or medical records in this form.
Disclaimer:
Submitting an inquiry does not enroll you in a clinical trial, constitute informed consent, or guarantee eligibility or participation. Participation in research is voluntary.