The PFAS study is looking for participants.

Are you in the third trimester of pregnancy? Participate in a study to test whether Munchkin Flow, a silicone breastfeeding nipple, could help new moms like you meet or exceed their breastfeeding goals.

Receive up to $595 via PayPal for your time

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What is this research about and why is it important?

The purpose of this study is to evaluate a reusable silicone breastfeeding cover that features a transparent milk channel, allowing moms to see when milk is flowing to their baby. The study team hopes that Flow's visual confirmation of breastmilk will boost confidence and encourage breastfeeding mothers to continue breastfeeding their infants.

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Who is this study for?

You may be qualified for this study to help us identify and correct these healthcare inequalities if:

You are 18 years or older

You are at least 37 weeks pregnant

You have access to an internet-enabled computer, smartphone or tablet

You are able to read and write in the English language and able to provide written informed consent to participate in this study.

What do I have to do to participate?

Get started on the steps below right now to qualify, and begin your participation in the study. Enrollment is online and easy. Earn up to $595 via PayPal.
To see if you qualify for the study:    

  • Take a short online survey to check if you qualify for the study.
  • You will learn more about the study and complete an online informed consent form
  • Over the course of up to 12 months, you will be asked to complete brief surveys.
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    Helpful resources

    Learn more about AI/AN healthcare inequities

    The Most Prevalent AI/AN Health Disparities (IHS)

    How Does Healthcare for Federally Recognized Tribes Work? (NCAI)

    Downloadable Educational Resources for AI/AN Patients (IHS)

    Learn more about clinical trial participation

    What does joining a clinical trial involve? (CISCRP)

    The basics of clinical trial participation (CISCRP)

    Clinical Participation Guide for AI/AN (UIHI)

    Frequently asked questions

    Why should I participate in this study?
    By participating in this study, you may provide valuable insights about healthcare experiences for American Indians or Alaska Natives.
    When and how will I be compensated?
    Participants will be compensated after completing certain study activities. You can receive up to $80 per visit including $50 for the screening visit, up to $30 per month for completing the monthly eDiary, and up to $590 if you complete all trial activities.
    What are the benefits and risks to participation?
    There are no risks associated with participation in this study. You will not be asked to take any medication or undergo any procedures directly for this study. 

    There are no guaranteed benefits from study participation. Information learned from the study may help inform future research around healthcare experiences for American Indians or Alaska Natives.
    Do I need to live on tribal lands to participate and/or have a doctor through the Indian Health Service (IHS)?
    No. This study is open to anyone who is American Indian or Alaska Native and has a first-time referral to an oncologist, neurologist, or ophthalmologist from a primary care or family doctor.
    Can I participate if I am already seeing an oncologist, neurologist, or ophthalmologist?
    You must have a first-time referral AND have not already visited that specialist to be eligible (exception: patients who are referred to an oncologist/cancer doctor and have already seen their specialist may still qualify)
    Can I stop being in the study?
    Yes. You can decide to stop at any time. Just tell the study researcher if you wish to stop being in the study. You do not need to give a reason why you want to stop participating.

    Also, the study researchers may ask you to stop taking part in this study at any time if they believe it is in your best interest, if you do not follow the study rules, or if the study is stopped.
    Who should I contact with questions?