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Obesity / overweight

Mothers and CareGivers Investing in Children Study 2.0

Recruiting · Austin, Texas

Always free

Study care at no cost to you

For your time and travel

Many studies pay you back

Most need no insurance or papers

Legal status usually isn't required; we'll tell you each study's requirements

Interpreters available

Ask for your language

Your choice

Voluntary — you can stop anytime

What is this study?

The study will use a longitudinal, randomized control trial design to determine intervention impact on parent and child behaviors, and infant health. The two intervention groups include: 1) MAGIC-FEED+; and 2) MAGIC-SAFE.

It is , overseen by an independent and licensed medical staff.

Read the full clinical description

The study will use a longitudinal, randomized control trial design to determine intervention impact on parent and child behaviors, and infant health. The two intervention groups include: 1) MAGIC-FEED+; and 2) MAGIC-SAFE. This trial is an efficacy trial of the MAGIC-FEED and MAGIC-SAFE program that has been successfully implemented with families as part of the MAGIC 1.0 program trial (IRB#: 2015040017). * The primary aim is to investigate each intervention's impact on infant BMIZ at 13 months. * The investigators will also assess the effect of MAGIC-FEED on caregiver nutrition knowledge and feeding practices, responsive feeding, infant diet, and child self-regulatory abilities and assess how these factors impact child self-regulation of eating and adiposity. * Finally, the investigators will determine if the interventions demonstrate the factors necessary to be a successful intervention as determined by the RE-AIM and PRISM frameworks.

Who this study is looking for

In plain language, from the study's own rules. The study team confirms the full details with you — this isn't a final yes or no.

✅ You may be able to join if…

  • A singleton baby who is 3–9 weeks old and was born at least 37 weeks into pregnancy.
  • The mother/caregiver is at least 18 years old.
  • The baby lives with the mother, and the primary caregiver identifies as the mother.
  • You live in the Austin metro area and plan to stay in Austin for the next two years.
  • You speak English or Spanish (families who only speak one of these are accepted; if you speak both plus other languages, you are still accepted).

🚫 You may not be able to join if…

  • Babies born before 37 weeks gestation.
  • Babies with major physical disabilities and/or a medical condition that affects feeding and growth.
  • Infants who had a NICU stay longer than 7 days.
  • Twins, triplets, or other multiple-birth infants.
  • Families who do not consent to video recording with the baby.

Are you a good fit?

Simplified highlights. The study team always confirms the full details with you.

  • Mother is at least 18 years old (primary caregiver is the mother).
  • You have a singleton baby 3–9 weeks old, born at ≥37 weeks.
  • Baby lives with mom and you’re in the Austin metropolitan area.
  • Family can communicate in English and/or Spanish and can consent to video recording.

How this study is designed

The real details, in plain words. Tap the underlined words to learn what they mean.

  • Some participants receive a . The study team tells you your chances of getting the active treatment before you decide.
  • You'd be placed into a group by chance, like a coin flip — this keeps the study fair.
  • This study is , so results can't be swayed by expectations. Your medical team always knows what you're getting.
  • There are 2 groups in this study.

What to expect, step by step

· This study lasts about 104 weeks (~24 months)
  1. 1

    Usually a few weeks

    The study team checks whether the study is a good fit for you, with a visit and sometimes lab tests. You can ask any questions before deciding.

  2. 2

    Treatment

    About 104 weeks

    If you join and choose to continue, you receive the study treatment and are watched closely by medical staff.

  3. 3

    Follow-up

    After treatment, the team checks on your health and confirms the visit schedule with you. You can leave the study at any point.

What's being tested

  • Behavioral: MAGIC-FEED
  • Behavioral: MAGIC-SAFE

Has this treatment been tested before?

The study team can share what safety testing has been done so far.

Who's running this study?

Sponsor

University of Texas at Austin

Overseen by Elizabeth Widen, PhD, RD, Deborah Jacobvitz, PhD

Every study is also reviewed by an independent that protects participants.

What you need to know before you apply

What is this study testing?+

The study will use a longitudinal, randomized control trial design to determine intervention impact on parent and child behaviors, and infant health. The two intervention groups include: 1) MAGIC-FEED+; and 2) MAGIC-SAFE.

Is it safe? Who makes sure of that?+

This is a research study. Every study is reviewed and monitored by an independent ethics board (called an IRB) whose job is to protect participants, and care is overseen by licensed medical staff. You'll be told the known risks before you agree to anything, and you can stop at any time.

Will I get a placebo instead of the real treatment?+

Some studies compare a treatment against a placebo (an inactive version), and some don't. If this one does, the study team will explain your chances of receiving the active treatment before you decide. Nothing is hidden from you.

Do I have to stop taking my current medications?+

It depends on the study. Some let you stay on your current medications and some ask you to adjust them. Never stop a medication on your own — the study team will review everything with you first.

Does it cost anything? Will I be paid?+

Study-related care is provided at no cost to you. Some studies also pay for your time; the coordinator can tell you if this one does. You should never be asked to pay to take part.

Do I need insurance? Will anyone ask about my immigration status?+

No. You do not need health insurance to take part in a research study, and you will not be asked about your immigration status to join. Taking part is about whether you're a medical fit for the study.

What if English isn't my first language?+

You have the right to understand everything before you agree. Study sites can often provide materials or an interpreter in your language — you can ask the coordinator for one.

Is my information private?+

Yes. Your health information is only shared with the study sites you choose to be contacted by, and only to help match and enroll you. It is never sold, and you can ask us to delete it at any time.

Source: ClinicalTrials.gov · NCT06719102 · Locations: Texas