Preventing Early Childhood Obesity, Part 1: Long-term Follow-up (PECO1-LTF)

Preventing Early Childhood Obesity, Part 1: Family Spirit Nurture, 3-9 Months, Long-term Follow-up

This study extends follow up on of Native American (NA) mothers and their children (now age 3-5 years) enrolled in the 1:1 randomized controlled trial of the Family Spirit Nurture (FSN) intervention designed to prevent early childhood obesity (PECO 1). The investigators will examine whether positive FSN impacts on sugar sweetened beverage (SSB) consumption and healthy growth in the first year of life were sustained. The investigators will also examine the effects of the emergency COVID-19 water solutions on water insecurity, early childhood SSB consumption, and growth, and explore how COVID-19 affected child feeding patterns and weight status either through changes in maternal mental health or household food access.

Study Overview

Detailed Description

Primary Aims

Aim 1. Determine the longer-term effectiveness of the brief FSN intervention on reducing SSB consumption, increasing water intake, and promoting healthy growth status up to 5 years of age.

Aim 2. Examine the impact of point-of-use (POU) water filters, employed as COVID-19 emergency water response efforts, on water insecurity, children's water intake and SSB consumption with or without previous FSN intervention. Positive findings would provide leverage to promote water solutions and water equity.

Secondary Aims

Secondary Aim 1. Determine whether providing a booster lesson at 4 years of age targeting age appropriate parental feeding practices, snack routines, avoidance of SSBs and increased water intake impacts SSB consumption and water intake between 4 and 4.5 years of age and child growth between 4 and 5 years of age.

Secondary Aim 2. Describe how COVID-19 affected child feeding patterns and weight status either through maternal depression and anxiety or changes in food access.

This follow-up study will builds upon a 1:1 randomized controlled trial of the Family Spirit Nurture (FSN) intervention designed to prevent early childhood obesity (PECO 1).

Methods:

A long-term follow-up evaluation will be conducted with n=110 of the randomized mother-child dyads (90% of the participants that completed the PECO 1 study) when the children are between 4 - 5 years of age.

Eligible participants will complete a 4 year follow-up assessment after reconsent when the children are 4 years of age. All participants will maintain their randomization status and receive one age appropriate lesson specific to their study group. The intervention group (n=55) will receive one FSN lesson focused on age-appropriate parental feeding practices, including snack routines, avoidance of SSBs, and increased water intake. The control group (n=55) will receive one injury prevention lesson focused on vehicle safety. An endline follow-up assessment will be completed by all reconsented participants after three months of the 4 year follow-up assessment. Maternal and child medical chart review will be conducted by trained study staff after the child turns 5 years old. Medical chart reviews will collect data on maternal BMI (as a possible moderator of child growth) and child growth.

During the COVID-19 pandemic as part of the emergency response on the Navajo Nation, a subset of study participants who previously reported water insecurity (n=50) received point-of-use (POU) water filters. Water filters were evenly distributed between the intervention (n=25) and control groups (n=25).

Study implementation will include three phases:

Phase 1 (Reconsent, Reenroll, and 4 year Follow-up Assessment):

Study staff will re-approach randomized mother/child dyads when the child is 4 years of age to complete the informed consent process for the follow-up component. Participants will maintain their original randomization status and complete a 4 year follow-up assessment that consists of a mixed-methods approach.

Phase 2 (Booster Lesson):

Local FHCs, trained and employed by Johns Hopkins, will deliver either the intervention (1- FSN lesson) or the control condition (1- Vehicle-Safety Lesson) shortly after the 4 year follow-up assessment when the child is 4 years of age. With participant permission, lesson visits will be audio recorded for quality assurance, using digital audio recorders. A random 10% of audio recordings will be reviewed and rated to ensure fidelity to the curriculum and to facilitate staff training and supervision.

Phase 3 (Endline Follow-up Assessment and Medical Chart Reviews):

Three months after the 4 year follow-up assessment, participants will complete an endline follow-up assessment. The endline follow-up assessment will be the same assessment battery as the 4 year follow-up assessment. Maternal and child medical chart reviews will be conducted by trained study staff after the child is 5 years of age. Weight and height data will be collected from child's medical charts (birth through 5 years of age). Data may be collected any time during the 5th year of life as timing of the five year check up can vary. Maternal BMI will be collected from maternal medical chart reviews as a possible moderator of child growth.

Study Type

Interventional

Enrollment (Actual)

110

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • New Mexico
      • Shiprock, New Mexico, United States, 87420
        • Johns Hopkins Center for American Indian Health

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

13 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Mother/child dyads who enrolled, participated in/completed the initial PECO 1 study (followed mother/infant dyads through 12 months of age).
  • Willingness to fully participate.

Exclusion Criteria:

  • Inability to participate in full intervention or evaluation (e.g., planned move, etc.)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Family Spirit Nurture (FSN)
Intervention group participants receive 1 Family Spirit Nurture lesson taught by Family Health Coaches. Mothers will receive the lesson within 1-2 weeks of completing the 4-year Follow-up Assessment. The lesson focuses on age-appropriate parental feeding practices, including snack routines, avoidance of SSBs and promotion of water consumption. The lesson is highly visual and interactive, and incorporates cultural teachings related to child feeding and nutrition that support aims. The Family Health Coaches also provide social support and will facilitate referrals to community resources.
The FSN intervention lesson is taught to participants previously randomized into the FSN intervention group during the PECO 1 study. Intervention group participants receive 1 Family Spirit Nurture lesson taught by Family Health Coaches. Mothers will receive the 1 - 45 minute lesson within 1-2 weeks of completing the 4-year Follow-up Assessment. The lesson focuses on age-appropriate parental feeding practices, including snack routines, avoidance of SSBs and promotion of water consumption. The lesson is highly visual and interactive, and incorporates cultural teachings related to child feeding and nutrition that support aims. The Family Health Coaches also provide social support and will facilitate referrals to community resources.
Other: Control Vehicle Safety
Control group participants receive 1 lesson with vehicle safety information, taught by Family Health Coaches. Mothers will receive the lesson within 1-2 weeks of completing the 4-year Follow-up Assessment. The Family Health Coaches also provide social support and will facilitate referrals to community resources.
The control (vehicle safety) lesson is taught to participants previously randomized into the control group during the PECO 1 study. Control group participants receive 1 - 30 minute lesson with vehicle safety information, taught by Family Health Coaches. Mothers will receive the lesson within 1-2 weeks of completing the 4-year Follow-up Assessment. The Family Health Coaches also provide social support and will facilitate referrals to community resources.
Other Names:
  • Vehicle Safety

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Group differences in children's mean BMI z-scores over time as assessed through child weight and length/height measurements through 5 years of age.
Time Frame: Birth to 5 years of age
Child weight (to the nearest ounce) and recumbent length/height (to the nearest 1/8 inch) will be extracted through medical chart review. Measurements will be taken by healthcare providers. Measurements will be used to calculate BMI z-scores using age- and sex-specific World Health Organization (WHO) Child Growth Standards.
Birth to 5 years of age
Group differences in sugar sweetened beverage (SSB) consumption & water intake.
Time Frame: 3 months to 5 years of age
Mothers were asked about SSB initiation and frequency among infants between 3 months and 12 months of age in the Preventing Early Childhood Obesity, Part 1: Family Spirit Nurture, 3-9 Months study using an an adapted version of the Pre-School-Aged Beverage Intake Questionnaire (BEVQ-15). We will continue to use the age appropriate Pre-School-Aged BEVQ-15 to assess child's SSB consumption and water intake between 4 and 5 years of age. This data will be examined for between group differences in SSB consumption and water intake through 5 years of age.
3 months to 5 years of age
Examine whether point-of-use (POU) water filters impact water security, and/or moderate intervention impact on water intake and SSB consumption.
Time Frame: 3 to 5 years of age
Examine the impact of point-of-use (POU) water filters, employed as COVID-19 emergency water response efforts, on water insecurity. Examine study group differences in water intake and SSB consumption with and without POU water filters.
3 to 5 years of age

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Between study group differences, post booster lesson, in age appropriate parental feeding practices, snack routines, avoidance of SSBs and increased water intake.
Time Frame: Up to 5 years of age
Age appropriate parental feeding practices, snack routines, avoidance of SSBs and increased water intake impacts SSB consumption and water intake between 4 and 4.5 years of age will be measured by the Toddler BEV-Q and Child Feeding Styles Questionnaire. Child growth between 4 and 5 years of age will be assessed by weight and length/height measurements from medical chart reviews.
Up to 5 years of age
Within study group comparison of pre-/during- COVID-19 child feeding practices, snack routines, SSB consumption and water intake and examination of associations with maternal depression and anxiety, and changes in food access.
Time Frame: 5 years postpartum
COVID-19 Impact Questionnaire will be used to assess how the COVID-19 pandemic has affected participants' lives, access to basic needs and healthcare, child feeding practices and childcare support. The Toddler BEV-Q and Child Feeding Styles Questionnaire will be used to assess child feeding practices, snack routines, SSB consumption and water intake. Maternal depression will be assessed by the CES-D and anxiety will be assessed by PROMIS Anxiety 8-item scale.
5 years postpartum

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Allison Barlow, Johns Hopkins Bloomberg School of Public Health

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 1, 2021

Primary Completion (Actual)

March 31, 2023

Study Completion (Actual)

August 15, 2023

Study Registration Dates

First Submitted

April 26, 2022

First Submitted That Met QC Criteria

June 15, 2022

First Posted (Actual)

June 21, 2022

Study Record Updates

Last Update Posted (Actual)

August 21, 2023

Last Update Submitted That Met QC Criteria

August 18, 2023

Last Verified

August 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 7476 /MOD994

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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