American Clinical Research Institute
Contact ACRI
ACRI helps people in the Dayton area explore studies that may fit their condition, understand what participation can involve, and connect with research staff for the next step.
Start Here
This first conversation is informational. Our team can explain available study areas and help you understand whether screening may be appropriate.
Browse current study categories such as anxiety, depression, migraine, IBS, gout, endometriosis, and more.
Complete the interest form for study matching, or contact ACRI directly if you want to speak with the team before sharing details.
If a study may be a fit, staff will explain visits, consent, privacy, possible risks, possible reimbursement, and participation expectations.
Participant Support
Taking part in research is voluntary. You can ask questions before signing an informed consent form, and you may stop participation according to the study guidance provided to you.
Study records are handled by authorized personnel and protected according to study requirements and applicable privacy rules.
The research team will explain study-related costs, covered procedures, and any available reimbursement before you decide.
ACRI offers weekday hours and flexible availability when participant and study needs require it.
Common Questions
These answers are general. The details can vary by study, and ACRI staff will explain the specific requirements before you choose whether to participate.
Study records and samples are handled according to study privacy requirements. Only the study doctor and authorized personnel can connect coded records with your identity, unless disclosure is required by law.
The study team will explain visit schedules, time commitments, responsibilities, and informed consent before you decide. If you participate, you will be asked to follow the study instructions provided by the research staff.
Study drugs or procedures may cause side effects or discomforts, and some risks may be unknown. You should tell the study doctor or study staff about any side effects or changes you notice.
Some studies use a placebo, which looks like the study drug but does not contain active medication. If a placebo is part of a study, the team will explain that possibility during the consent process.
Your symptoms may or may not improve. Participation can also provide information that may help future patients. The study team will explain possible benefits and risks for the specific study.
Participation is voluntary. You may discontinue participation according to the study guidance provided to you, without penalty or loss of benefits to which you are otherwise entitled.
The study team will explain which study-related drugs, visits, or procedures are covered before you decide. Details can vary by study.
Some studies may offer reimbursement for travel, meals, or time. The research team will explain any available reimbursement for the study you are considering.
Next Step
Use the dedicated interest form to share your contact details, health conditions, and study interests. This is only an interest form; a staff member will contact you before any screening or consent process.
Usually takes a few minutes to complete.
Tell us the condition or study area you are interested in. Our team will follow up with the next step.