
Frequently Asked Questions (FAQ)
For Research Participants
Thinking About Participating in a Research Study?
We know that joining a research study can raise a lot of questions. Whether you're here to learn more or are already participating in a Phronetik-led study, we want to make sure you have the information you need to feel confident and safe.
General Questions
❓ What is research involving human participants?
Research involving human participants is a structured investigation designed to answer health-related questions. It may involve interviews, surveys, blood draws, health records, wearable devices, or clinical procedures.
❓ Why should I participate in research?
By participating in research, you contribute to discoveries that improve health care, advance science, and benefit future generations. Some studies may offer access to new treatments or health insights.
❓ Do I have to participate?
No. Participation is completely voluntary. You can say no or withdraw from a study at any time for any reason, without penalty or loss of services you are otherwise entitled to.
❓ Will I be paid?
Some studies offer compensation for your time, travel, or effort. If compensation is provided, this will be explained during the consent process.
Privacy and Safety
❓ Is my personal information safe?
Yes. We take your privacy seriously. All research at Phronetik is reviewed by our Institutional Review Board (IRB) to ensure your identifiable information is protected in accordance with HIPAA and federal guidelines.
❓ What if I get hurt during the study?
In the rare event of an injury related to a research study, you’ll be informed about what support or care is available. This will be covered in the informed consent form before you agree to join.
❓ Who reviews and approves these studies?
Every research study at Phronetik is reviewed by our Institutional Review Board (IRB), which includes scientists, ethics experts, and community members. The IRB’s job is to protect your rights and safety.
Before & During Participation
❓ What is informed consent?
Informed consent is a process where you learn about a study’s purpose, risks, benefits, and your rights. You must give written permission before joining. You can ask questions and take time to decide.
❓ Can I change my mind after I join a study?
Yes. You can withdraw at any time, even after you’ve signed the consent form. Just notify the research team.
❓ What if I don’t understand something in the study?
Ask! We encourage you to reach out at any time. Our team is here to help you understand the study every step of the way.
After Participation
❓ Will I get the results of the study?
In some cases, yes. Ask the study team whether individual or overall study results will be shared. Keep in mind that research can take time, and some studies may not release individual results.
❓ Who do I contact with questions or concerns?
You can contact the Phronetik OSR or study staff directly.
📧 osr@phronetik.com
📞 (844) 871.3575
If you feel your rights have been violated or you wish to speak with someone not directly involved in the study, you may also contact the Office for Human Research Protections (OHRP) at www.hhs.gov/ohrp.
Still Have Questions?
Visit our Participant Rights & Responsibilities page or reach out to us directly. We are here to support you.

Quick Access
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[IRB Submission Portal]
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[Request a Single IRB (sIRB) Agreement]
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[Report an Adverse Event or Protocol Deviation]
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[IRB Policies & SOPs]
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[Data Privacy & HIPAA Guidelines]