Explore research, at your own pace

An introductory conversation is a chance to ask questions; it is not enrollment or a promise of testing. Before arranging a study visit, ask the team to confirm that the study is recruiting at IHR and that the required approvals are in place.

If a study is available, ask about its purpose, visits, risks, possible benefits and alternatives. Study-specific clinical screening depends on the approved study plan and the required informed consent process before testing. Confirm the purpose of your appointment and what to bring. Use the first-visit checklist.

First ask whether a specific study is recruiting at IHR. If one is available, the team can explain its requirements, which may include age, health history and current medicines. Eligibility depends on that study’s criteria and the appropriate screening process. Contacting us or submitting a form does not confirm eligibility, reserve a place or enroll you. Share contact details only; ask the team how to provide any medical information.

No. You can ask questions and review your options before deciding. A website form is not informed consent for a study.

That depends on the study. The team explains any amounts, conditions and payment schedule in the study information and consent. Do not assume payment is offered for every study.

Research can involve risks, and personal benefit is not guaranteed. Some studies use a placebo or comparison treatment. Ask the team to explain the study-specific risks, possible benefits and alternatives.

Participation is voluntary. Discuss withdrawal with the study team, including any recommended follow-up and how information already collected will be handled.

Use this website for basic contact details only. Do not send medical records, diagnoses, test results, Social Security numbers or insurance details through public forms, the chatbot or general email.

Before sharing health information, ask the team which channel to use and request the applicable privacy documents. Ask who may access your information, how it may be used or shared, and how it is stored and retained. Website contact permission is separate from study consent and any HIPAA authorization that may apply. Read privacy and participant-rights information.

Confirm your visit schedule and who to contact if you cannot attend, have a concern or need instructions outside office hours. Use the study team’s agreed channel for health information.

Ask what follow-up is needed, who will coordinate your ongoing care and how to request the study’s overall results when available. Ask the study clinician about any medication instructions. Follow-up and access to a study treatment depend on the protocol; they are not guaranteed by this website.