1
Our staff will welcome you and walk you through the purpose of the visit. No need to prepare anything in advance.
2
A physician will walk you through the Informed Consent Form — explaining the study, risks, benefits, and what's expected. A translator can be provided if needed.
3
Free physical exam, blood and urine tests to determine eligibility. All at no cost to you.
4
If you qualify, a coordinator schedules your first official study visit. If you don't, you'll still be compensated for your time and travel.
Clinical trials are research studies that explore whether new medical approaches — medications, devices, procedures, or behavioral strategies — are safe and effective in people. They are the most reliable way to evaluate whether a new treatment works.
All studies at Solace Clinical Research are FDA-approved and supervised by licensed physicians.
Before joining any study, you’ll go through an informed consent process. A coordinator — along with the physician overseeing the study — will explain everything: the purpose of the trial, known risks and benefits, what procedures are involved, how long it lasts, and your rights as a participant. A translator can be provided if English is not your first language. Signing the consent form does not lock you in — you can withdraw at any time.
No. No health insurance, Social Security Number, or citizenship documentation is required to participate. Eligibility is determined by the medical criteria of each specific study — not by your documentation or immigration status.
If you don’t qualify for a current study, we’ll keep your information on file and reach out when a matching trial becomes available. You’ll also be compensated for any screening visit you attend, regardless of the outcome.
Yes. All participants are compensated for their time and travel at each completed study visit. Compensation amounts vary per study and per visit type, and everything will be clearly outlined in your Informed Consent Form before you begin. You can also contact our staff at any time with questions about payments.
Clinical trials are research studies that explore whether new medical approaches — medications, devices, procedures, or behavioral strategies — are safe and effective in people. They are the most reliable way to evaluate whether a new treatment works.
All studies at Solace Clinical Research are FDA-approved and supervised by licensed physicians.
Before joining any study, you’ll go through an informed consent process. A coordinator — along with the physician overseeing the study — will explain everything: the purpose of the trial, known risks and benefits, what procedures are involved, how long it lasts, and your rights as a participant. A translator can be provided if English is not your first language. Signing the consent form does not lock you in — you can withdraw at any time.
No. No health insurance, Social Security Number, or citizenship documentation is required to participate. Eligibility is determined by the medical criteria of each specific study — not by your documentation or immigration status.
If you don’t qualify for a current study, we’ll keep your information on file and reach out when a matching trial becomes available. You’ll also be compensated for any screening visit you attend, regardless of the outcome.
Yes. All participants are compensated for their time and travel at each completed study visit. Compensation amounts vary per study and per visit type, and everything will be clearly outlined in your Informed Consent Form before you begin. You can also contact our staff at any time with questions about payments.
