This confidential screener takes approximately 3–4 minutes and helps our clinical team assess your compatibility with current and upcoming research studies exploring device-based therapies for treatment-resistant depression.
This should be a diagnosis made by a licensed psychiatrist, psychologist, or physician. A self-reported or suspected diagnosis does not qualify at this stage.
Duration of illness is an important factor in determining eligibility for certain neuromodulation protocols. Please select the option that best reflects your experience.
Please reflect on the past two weeks when selecting your response.
This helps us understand the full scope of your experience.
Include all medications prescribed by a doctor for depression where you did not achieve significant symptom improvement, regardless of whether you completed the full course.
Select every category you've been prescribed, even if you've only tried one medication from that class.
Understanding your current situation helps us determine which studies you may be eligible for right now.
This includes any device-based, procedural, or interventional treatments you may have received for depression.
Most of our active trials require participants to be between 22 and 70 years of age. Age criteria vary by specific study protocol.
Neuromodulation trials typically require regular in-person visits to a study site over 6–24 months. Some visits may be weekly, particularly in the early phases.
A clinical coordinator will personally review your screening responses and reach out within 48 hours to discuss next steps.
Please complete all fields before submitting.
By submitting this form, you consent to being contacted by the Broaden Study research team. Your information will not be shared with third parties. This screener does not constitute medical advice or a guarantee of trial eligibility.
Based on your current responses, you may not meet the eligibility criteria for our active trials. Clinical trial criteria can be very specific and this is not a reflection of the severity of your experience.
Stay connected as new studies open.
New trials enroll regularly. By joining our newsletter, you'll be among the first to know when eligibility criteria change or new research studies become available.
✓ You're on the list. We'll be in touch when new studies open.
If you believe you received this result in error, or if your situation changes, you can retake the screener at any time. Questions? study@broadenstudy.com
Your information has been securely submitted. A clinical coordinator will review your eligibility profile and reach out within 48 hours to discuss potential next steps and answer any questions.
What happens next?
Questions in the meantime? Reach us at study@broadenstudy.com