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CompletedNCT06520072MAPPUpdated Jun 3, 2026

Mobile Apps for Preschool Parents (MAPP) Study

An interventional study of Children Eating Well (CHEW) mobile app and Beanstalk mobile app in Obesity, Childhood, Nutrition, Healthy and Physical Inactivity, sponsored by Pamela Hull. Completed at 1 site in United States. Open to participants aged 18 Years to 99 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-03.

Sponsored by Pamela Hull · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
224
Allocation
Randomized
Ages
18 Years to 99 Years
Sex
All
01

Study summary

The purpose of Mobile Apps for Preschool Parents (MAPP) Study is to test the effectiveness of two mobile applications for parents of preschool aged children: 1) an app focused on child and family nutrition and wellness, and 2) an app focused on parents reading to their children.

Read the detailed description

The Mobile Apps for Preschool Parents (MAPP) Study addresses an important gap in the scientific literature, which is the need to evaluate the use of parent-targeted, guided goal-setting for childhood obesity risk reduction via a mobile application, specifically for parents of preschool-aged children for early intervention.

Obesity is a leading cause of multiple chronic diseases, including 13 types of cancer, heart disease, stroke, and type II diabetes. Major behavioral determinants of obesity are also independent risk factors for these chronic diseases, including unhealthy diet, lack of physical activity, and poor sleep quality. Childhood obesity increases risk for adult obesity and early onset of conditions such as high blood pressure, high cholesterol, asthma, sleep apnea, and joint problems. Childhood obesity disproportionately affects children of lower socioeconomic status, racial/ethnic minority groups, and rural areas, thus exacerbating and contributing to health disparities among obesity-related health conditions. Children in low-income families that qualify for income-based public assistance programs represent a population that is at high risk for obesity. These programs include the Women, Infants and Children (WIC) Supplemental Nutrition Program; Head Start (preschool child care centers); the Supplemental Nutrition Assistance Program (SNAP); Temporary Assistance for Needy Families (TANF); and Medicaid.

With the Attention Control Arm, the MAPP Study will also contribute valuable information about the effectiveness of using a mobile application with parent-targeted, guided goal-setting for reading to preschool-aged children. Previous studies have shown that adults reading to children is beneficial for child learning and development.

All parents/guardians (both samples and both arms) will be asked to use the respective apps for an 8-week intervention period. The primary outcome will be measured in the Baseline Survey and a Follow Up Survey after completing the 8-week intervention period. After completion of the Follow Up Survey, parents/guardians will be given the option to download and use the other app, if they are interested (i.e., information about the CHEW app for the Control Arm, and information about the Control app for the Intervention Arm). For both the Intervention Arm and those who choose to download the CHEW app in the Control Arm, usage of the CHEW app (i.e., app analytics) will be tracked for up to 20 weeks after the date of study enrollment.

02

Conditions studied

  • Obesity, Childhood
  • Nutrition, Healthy
  • Physical Inactivity
  • Sleep, Inadequate

Keywords

  • Mobile Application
  • Preschool children
  • Parents
  • Parenting
  • Reading
03

In context

Pediatric Obesity

1,129 studies on the registry are indexed under Pediatric Obesity; 187 are open to participants now.

This study's enrollment of 224 is above the median of 100 across 870 interventional studies indexed under Pediatric Obesity.

Browse Pediatric Obesity studies →

Lead sponsor

Pamela Hull is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Parent/Guardian (age 18+ years) of a 2-5 year old
  • Living in United States
  • Receives services at partner community organization (Organization Sample only)

Exclusion criteria

Exclusion Criteria:

  • Does not own iOS/Apple or Android mobile device (phone or tablet)
  • Does not have internet access for the mobile device (data plan on device or in-home WiFi)
  • Not able to successfully load and access the Intervention Arm or Attention Control Arm mobile app on the mobile device at the time of enrollment
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
224 participants (actual)

Study arms

  • Experimental
    Intervention Arm: Nutrition and wellness app

    The parents/guardians in this study arm will use the Children Eating Well (CHEW) mobile app focused on child and family nutrition and wellness for the first 8 weeks of the study. This app is designed to help parents/guardians of preschool-aged children to improve nutrition, physical activity, sleep, feeding children at mealtimes, and related wellness topics.

    Behavioral: Children Eating Well (CHEW) mobile app

  • Active comparator
    Attention Control Arm: Reading app

    The parents/guardians this study arm will use the Beanstack mobile app (or the Bookroo app, as an alternative) focused on parents reading to their children for the first 8 weeks of the study. This app may help parents/guardians to read more to their preschool children (and other children), which is good for child learning and development.

    Behavioral: Beanstalk mobile app

Interventions

  • BehavioralChildren Eating Well (CHEW) mobile app

    The target users of the CHEW app are parents/guardians of preschool aged children. The purpose of the CHEW app is to provide parents/guardians with easy, practical ways to improve nutrition and wellness among their preschool-aged children. The app provides guided goal setting and tracking tools. Parents/guardians set goals related to their preschool-aged children focused on nutrition, physical activity, sleep behaviors and parenting styles. The parents/guardians can also to set goals for themselves for behaviors related to nutrition, physical activity, sleep, and stress. The app does not have features that target children as users. The CHEW app was developed by the study team and can be downloaded for mobile devices (phones or tablets) at no cost in the Apple App Store (iOS/Apple) and the Google Play Store (Android). After downloading the CHEW app, enrolled participants must enter the Access Code provided by the study team in order to unlock the app and use it.

  • BehavioralBeanstalk mobile app

    Beanstack is free commercially-available mobile app that provides goal setting and tracking tools similar to the CHEW app, but focused on a different topic, specifically encouraging parents/guardians to read to their preschool children more frequently. In the case that a parent/guardian is not able to successfully download Beanstack to their mobile device, as a backup alternative they will be asked to use a similar free commercially-available mobile application called Bookroo. Beanstack is available to the public for mobile devices (phones or tablets) at no cost in the Apple App Store (iOS/Apple) and the Google Play Store (Android). Bookroo is a web-based application that users access via the mobile device's web browser and looks and functions like a regular mobile application. It should work on any mobile device with a browser and data/wifi access,

    Also known as: Alternative: Bookroo mobile app

06

What researchers measure

Primary outcomes

  1. Healthy Kids childhood obesity risk score

    Using the 19-item Healthy Kids scale, each item is coded from 1 to 5, with 1 being the least healthful and 5 being the most healthful. To calculate the childhood obesity risk score, all 19 items are summed together, ranging from 19 to 95, with higher values reflecting a more healthful, or positive, outcome.

    Time frame: 2 months

Secondary outcomes

  1. Child intake of sugar-sweetened beverages (Healthy Kids items)

    Child intake of sugar-sweetened beverages (Healthy Kids items)

    Time frame: 2 months

  2. Child intake of fruits and vegetables (Healthy Kids items)

    Child intake of fruits and vegetables (Healthy Kids items)

    Time frame: 2 months

  3. Child intake of energy dense food/beverages (Healthy Kids items)

    Child intake of energy dense food/beverages (Healthy Kids items)

    Time frame: 2 months

  4. Child intake of dairy/calcium (Healthy Kids items)

    Child intake of dairy/calcium (Healthy Kids items)

    Time frame: 2 months

  5. Child physical activity and sedentary behavior (Healthy Kids items)

    Child physical activity and sedentary behavior (Healthy Kids items)

    Time frame: 2 months

  6. Sleep: Child bedtime (Healthy Kids item)

    Child bedtime (Healthy Kids item)

    Time frame: 2 months

  7. Family meals: Eating meals with child (Healthy Kids item)

    Eating meals with child (Healthy Kids item)

    Time frame: 2 months

  8. Child dietary intake (Healthy Kids items)

    Child dietary intake (Healthy Kids items)

    Time frame: 2 months

  9. Diet quality: Variety of child vegetable intake (My Veggies questionnaire)

    Variety of child vegetable intake (My Veggies questionnaire)

    Time frame: 2 months

  10. My Child at Mealtime questionnaire

    My Child at Mealtime questionnaire measures food-related parenting styles.

    Time frame: 2 months

  11. Home Inventory Describing Eating and Activity (Home-IDEA2, food section)

    Home Inventory Describing Eating and Activity (Home-IDEA2, food section) measures home food environment.

    Time frame: 2 months

  12. Frequency of reading to child

    Frequency of reading to child

    Time frame: 2 months

  13. Length of time reading to child

    Length of time reading to child

    Time frame: 2 months

07

Study locations

1 site
  • University of Kentucky
    Lexington, Kentucky 40536, United States
08

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Aug 2024 to primary completion in Nov 2024, 3 months.

Of 539 non-industry interventional studies with no phase under Pediatric Obesity, half reached primary completion within 25 months of starting (the median), counting those still running; a quarter within 11 and three quarters within 45. This study's 3 months is below that.

Counting every sponsor, half of 541 studies reached it within 25 months; a quarter within 11 and three quarters within 45.

How these figures are worked out, and which studies are left out of them.

Registered
Jul 22, 2024
First posted
Jul 25, 2024
StartActual
Aug 1, 2024
Primary completionActual
Nov 19, 2024
CompletionActual
Nov 19, 2024
Last update
Jun 3, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06520072
Lead sponsor
Pamela Hull
Collaborators
United States Department of Agriculture (USDA)
Responsible party
Pamela Hull (Associate Professor, University of Kentucky) — Sponsor-investigator
First posted
Jul 25, 2024
Start date
Aug 1, 2024
Primary completion
Nov 19, 2024
Completion
Nov 19, 2024
Last update
Jun 3, 2026

Study contacts

Pamela C Hull, PhD
principal investigator · University of Kentucky

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in May 2026. You cannot join it, but the record below documents what was studied.

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