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Obesity, ChildhoodMAGICNCT04177472

Mothers And careGivers Investing in Children

A study testing Obesity Prevention Group, Obesity Prevention Group + Food Boxes and Infant Safety and Injury Prevention Group in people with Obesity, Childhood and Parenting, run by University of Texas at Austin at 2 sites in United States.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

The incidence of childhood obesity in the United States has steadily increased over the past 30 years but has begun to level off in recent years. Epidemiological evidence indicates that obesity may transmitted across multiple generations. Read more about this study

Who is it for?
Ages 0 to 90 yearsHealthy volunteers can take part
Conditions the study is for
Obesity, Childhood, Parenting
What is being tested?
Obesity Prevention Group, Obesity Prevention Group + Food Boxes and Infant Safety and Injury Prevention Group
Could I receive a placebo?
No, everyone receives an active treatment
How many people
165 participants
Where
2 sitesUnited States
Study dates
14 Nov 2019to 31 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 0 to 90 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Mothers with babies aged 4 to 5 months
  • Other caregivers assisting the mother with the baby.
  • Babies aged 4 to 5 months

Who cannot join

  • Babies with metabolic or feeding issues.
  • Mothers younger than 16 years of age.

Trial locations and contacts

2 sites in 1 country.

United States2 sites
  • Sarah M. & Charles E. Seay Building

    Austin, Texas, 78712

  • Dell Pediatric Research Institute

    Austin, Texas, 78723

Other trials in United States

About this study

Official title: MAGIC: A Family Based Feeding Intervention Program

The incidence of childhood obesity in the United States has steadily increased over the past 30 years but has begun to level off in recent years. Epidemiological evidence indicates that obesity may transmitted across multiple generations. The current study seeks to: 1) evaluate the extent to which mothers and other important caregivers affect their mothers' parenting; 2) examine whether an intervention aimed at improving diet quality and enhancing responsive feeding to improves parental responsivity and feeding behavior and infants' weight trajectories over time; 3) examine the effects of early life feeding and caregiver sensitivity on health and development; and 4) examine feasibility of food distribution along with the feeding intervention.

Read the detailed description

The incidence of childhood obesity in the United States has steadily increased over the past 30 years, but has begun to level off in recent years. Children from minority groups may be disproportionately affected, such that Hispanic and non-Hispanic Black children have greater weight for recumbent length compared to White children. Similarly, socioeconomic status (SES) may affect child weight status. Epidemiological evidence indicates that obesity may transmitted across multiple generations. Genetics are a factor in determining weight status, but parents are largely responsible for regulating children's dietary environments. Grandparents increasingly provide care for their grandchildren, yet few studies have examined grandparent involvement or the role that grandparents or other significant caregivers play in feeding the child.

The objective of the current study is two-fold: 1) to evaluate the extent to which mothers and other caregivers affect mothers' parenting surrounding feeding their infant, beginning when the infant is first introduced to solid foods; and 2) to examine whether an intervention aimed at providing both mothers and and other important caregivers with hands-on training regarding healthy foods and responsive and sensitive feeding behaviors improves mothers' and other caregivers' responsive and sensitive behaviors and infants' weight trajectories over time. The researchers will collect both self-report data on diet, child temperament, mothers and caregiver mental health, stress and support. Observational assessments will be obtained to code co-caregiver behavior and caregiver responsiveness during feeding.

Being tested
Obesity Prevention Group, Obesity Prevention Group + Food Boxes, Infant Safety and Injury Prevention Group
Keywords
nutrition, parenting, intergenerational feeding influences, sensitive feeding
Medical subject headings
Pediatric Obesity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Obesity Prevention GroupBehavioural

    Parents will be provided with responsive feeding coaching to help them recognize hunger and satiety cues and nutrition coaching that involves recommending a sequence of introducing complementary foods that corresponds with food textures and feeding styles, breast/bottle weaning, healthy snacking and hands on demonstrations for healthy food options.

  • Obesity Prevention Group + Food BoxesBehavioural

    Parents will be provided with responsive feeding coaching to help them recognize hunger and satiety cues and nutrition coaching that involves recommending a sequence of introducing complementary foods that corresponds with food textures and feeding styles, breast/bottle weaning, healthy snacking and hands on demonstrations for healthy food options. Parents will also be provided with grocery items (fruits, vegetables, meat) prior to each intervention visit to facilitate a healthy family diet.

  • Infant Safety and Injury Prevention GroupBehavioural

    Parents will be provided with information about safe sleeping, car seats, baby-proofing, etc., delivered during home visits, newsletters, and reinforcing text messages.

Study groups in NCT04177472
Study groupRoleWhat they receive
Obesity Prevention GroupExperimentalParents will be provided with responsive feeding coaching to help them recognize hunger and satiety cues and nutrition coaching that involves recommending a sequence of introducing complementary foods that corresponds with food textures and feeding styles, breast/bottle weaning, healthy snacking and hands on demonstrations for healthy food options.
Receives: Behavioral: Obesity Prevention Group
Infant Safety and Injury Prevention GroupActive comparatorParents will be provided with information about safe sleeping, car seats, baby-proofing, etc., delivered during virtual visits, participant binder and newsletter.
Receives: Behavioral: Infant Safety and Injury Prevention Group
Obesity Prevention Group + Food BoxesExperimentalParents will be provided with responsive feeding coaching to help them recognize hunger and satiety cues and nutrition coaching that involves recommending a sequence of introducing complementary foods that corresponds with food textures and feeding styles, breast/bottle weaning, healthy snacking and hands on demonstrations for healthy food options. Parents will also be provided with grocery items (fruits, vegetables, meat) prior to each intervention visit to facilitate a healthy family diet.
Receives: Behavioral: Obesity Prevention Group + Food Boxes

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. BMI percentile at 12 months of age

    Anthropometrics measured by trained study staff

    Measured: 12 months

  2. BMI percentile at 24 months of age

    Anthropometrics measured by trained study staff

    Measured: 24 months

Secondary outcomes (2)
  1. Proportion of infants with BMI percentile >85th at 12 months of age

    Anthropometrics measured by trained study staff

    Measured: 12 months

  2. Proportion of infants with BMI percentile >85th at 24 months of age

    Anthropometrics measured by trained study staff

    Measured: 24 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Nov 2019
  2. Study start14 Nov 2019
  3. Primary completion31 May 2026 (estimated)
  4. Study completion31 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
165 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04177472
Sponsor's protocol ID
UT Austin IRB#2015040017
Acronym
MAGIC
Status last verified
Mar 2026
First submitted
25 Oct 2019
Last updated
28 Apr 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Obesity Prevention Group, Obesity Prevention Group + Food Boxes and Infant Safety and Injury Prevention Group in people with Obesity, Childhood and Parenting, run by University of Texas at Austin at 2 sites in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 28 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

BMI percentile at 12 months of age (time frame: 12 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Apr 2026.

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