Using Family-Based Approaches to Improve Healthy Eating for Southeast Asian Children

May 14, 2026 updated by: Brown University

Testing a Multilevel, Multicomponent, Multigenerational Dietary Intervention to Improve Southeast Asian Children's Diets

This small scale healthy eating study provides Southeast Asian families with children ages 6 to 11 with a family-based nutrition education, one-on-one interviews to help with motivation to eat health, text messaging, and coupons to purchase health foods and beverages. Since this is a small scale study that is a pilot intervention, the main goal of this intervention is to determine if it is feasible, meaning, can it be done. The second goal of this intervention is to determine if there are meaningful improvements in children's healthy eating patterns, body mass index and HbA1c. The third goal is to see if the intervention improves parent's diet quality, HbA1c and the home food environment. These study findings will be used to determine whether a larger clinical trial is needed, and if so, how it should be done.

Study Overview

Detailed Description

This intervention reflects the investigative team's eight year and ongoing academic-community research partnership with the Center for Southeast Asians (SEA) in Rhode Island, formative work with SEA families, and the team's extensive experience conducting successful dietary interventions. The current study is a pilot feasibility study that tests an innovative multilevel, multicomponent, multigenerational dietary intervention to improve diet quality among SEA children.

75 SEA families with children ages 6 to 11 years will be recruited from Providence County, Rhode Island. Adult-child pairs will be randomized to: (1) financial incentive only arm that will receive weekly $15 financial incentive coupons to subsidize purchase of healthy foods at a local SEA grocery store; or (2) financial incentive plus twice-monthly, family-based group nutrition education at the Center for SEA led by SEA community health workers; three motivational interviewing (MI) calls by trained community health workers; dietary norms messaging for adults (via weekly text messages) and for children (via Infographics at nutrition education sessions); and weekly $15 financial incentive coupons to subsidize purchase of healthy foods at SEA grocery stores; or (3) an Academic Engagement attention control arm that will follow the structure of the financial incentive plus nutrition education, MI and text messages and infographics arm. The primary outcomes are study feasibility and clinically meaningful improvement in child's diet quality (measured by healthy eating index). Secondary outcomes are clinically meaningful changes in children's body mass (~ 2kg weight loss or no weight gain), HbA1c (0.5%) and parent's diet quality, HbA1c and the home food environment. These study findings will be used to inform a future, larger clinical trial.

Study Type

Interventional

Enrollment (Actual)

114

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

    • Rhode Island
      • Providence, Rhode Island, United States, 02912
        • Brown University

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria for Adults:

  • Hmong, Cambodian, Laotian or Vietnamese
  • the child's parent, legal guardian or grandparent
  • live with the child
  • age 18 or older
  • knowledgeable about the child's diet
  • responsible for household food preparation
  • read/speak English, Hmong, Khmer, Vietnamese and/or Lao
  • own a smartphone
  • be willing to shop at the partner SEA grocery store

Exclusion Criteria for Adults:

  • participation in weight-related studies in the past 12 months
  • medical conditions that would affect participation (e.g., hospitalization due to type 2 diabetes in past year)

Inclusion Criteria for Children:

  • Hmong, Cambodian, Laotian or Vietnamese
  • age 6 to 11 years
  • read/speak English
  • Veggie Meter score ≤400

Exclusion Criteria for Children:

  • disabilities that would affect participation
  • chronic conditions affecting growth or diet
  • medications affecting weight or metabolism

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Attention control: Academic Engagement
This intervention will be delivered using a similar format and schedule as the financial incentive+nutrition education, motivational interviewing and dietary norms intervention group (i.e., 11 community health worker led in-person group based sessions at the Center for Southeast Asians, 3 MI phone calls, and text messages). The content will focus on family-specific family engagement methods to improve children's academic outcomes.
For six months, families will attend in-person, group-based school engagement education with other Southeast Asian families designed to improve youths' academic outcomes. Families will receive text messages and motivational interviews. At the end of the six months, families will receive the equivalent of the six months worth of weekly, $15 financial incentives.
Experimental: Financial incentive only
Participants will receive weekly financial incentive coupons to purchase eligible foods at the partnering Southeast Asian grocery store. Research Assistants will explain the coupon procedures during the randomization phone call. Research Assistants will mail the adult a schedule of coupon disbursement dates. RAs will mail one month's worth of coupons (4, $15 coupons) to each adult's home. Coupons will be used at point-of-sale. Participants' will receive an automated weekly text message via Qualtrics directing them to upload their photos to the system if they used coupons during that week.
For six months, families will receive weekly, $15 financial incentives to purchase healthy foods and beverages at a partnering Southeast Asian grocery store
Experimental: Financial incentive + nutrition education, motivational interviewing, dietary norms messages
The intervention consists of a) four $15 financial incentive coupons each month; b) twice-monthly group-based nutrition education at the Center for SEA; c) motivational interviewing (months 1, 3, 5); and d) weekly dietary norms text messages sent to adults and twice-monthly dietary norms infographics presented at nutrition education sessions for children. The research assistants will disburse one months' worth of the financial incentive coupon at the nutrition education sessions (or home mailings for absent participants). Families will attend 11 fortnightly, group-based nutrition education sessions lasting one hour. Southeast Asian community health workers will lead the sessions. Research assistants trained in motivational interviewing will call the adults. The calls will last 15-20 minutes. Adults will receive a series of weekly, interactive descriptive dietary norms text messages. Children will see descriptive dietary norms infographics at children's nutrition education sessions.
For six months, families will receive weekly, $15 financial incentives to purchase healthy foods and beverages at a partnering Southeast Asian grocer store, in-person, group-based nutrition education with other Southeast Asian families, text messages and motivational interviewing

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Feasibility of Study Methods As Assessed by Rate of Participant Enrollment Each Month
Time Frame: Study enrollment to six-month follow-up
Feasibility will be demonstrated if 7 enrolled Southeast Asian families per month are recruited on average over 12 months
Study enrollment to six-month follow-up
Feasibility of Study Methods As Assessed by Participant Retention at 6-Months Study Completion
Time Frame: Study enrollment to six-month follow-up
Feasibility will be demonstrated if 80% of enrolled families are retained at 6 months
Study enrollment to six-month follow-up
Feasibility of Study Methods As Assessed by Participant Attendance at Group Sessions at 6-Months Study Completion
Time Frame: Study enrollment to six-month follow-up
Feasibility will be demonstrated if 0% of enrolled families attend in-person sessions
Study enrollment to six-month follow-up
Acceptability of the Intervention As Assessed by Participant Favorability Rating of the Intervention at Six-Months
Time Frame: Study enrollment to six-month follow-up
Acceptability for each intervention component will be achieved if at least 70% of participants rate the component as "favorable" or "very favorable" on the measure of acceptability
Study enrollment to six-month follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Diet quality as Assessed by 24-Hour Dietary Recall - Child
Time Frame: Study enrollment to six-month follow-up
24-Hour dietary recall data will be converted to Healthy Eating Index scores to provide overall and subcomponent scores.
Study enrollment to six-month follow-up
Fruit and vegetable intake as Assessed by The Veggie Meter - Child
Time Frame: Study enrollment to six-month follow-up
Children's fruit and vegetable intake will be determined using the Veggie Meter, which is an objective measure of dermal carotenoids over a two month period.
Study enrollment to six-month follow-up
Height ( Meters) as Assessed by Portable Stadiometer - Child and Adult
Time Frame: Study enrollment to six-month follow-up
Objectively assessed height will be measured by research assistants using a portable stadiometer.
Study enrollment to six-month follow-up
Weight (Kilograms) as Assessed by Tanita Body Scale - Child and Adult
Time Frame: Study enrollment to six-month follow-up
Objectively assessed weight will be measured by research assistants using the Tanita Body Weight Scale.
Study enrollment to six-month follow-up
Body Mass Index (BMI) as Assessed by the Ratio of Height/Weight (kg/m^2) - Child and Adult
Time Frame: Study enrollment to six-month follow-up
Weight and height measures will be combined to compute Body Mass Index. Body Mass Index will be determined using appropriate child and adult reference values, respectively.
Study enrollment to six-month follow-up
Waist Circumference (Inches) as Assessed by Seca Flexible Tape Measure - Child and Adult
Time Frame: Study enrollment to six-month follow-up
Objectively assessed waist circumference will be measured by research assistants. Waist circumference categories will be determined using appropriate child and adult reference values, respectively.
Study enrollment to six-month follow-up
Height (Feet and Inches) as Assessed by Portable Stadiometer - Child and Adult
Time Frame: Study enrollment to six-month follow-up
Objectively assessed height, weight and waist circumference will be measured by research assistants. Body Mass Index and waist circumference categories will be determined using appropriate child and adult reference values, respectively.
Study enrollment to six-month follow-up
Beverage Intake as Assessed by the Beverage Intake Questionnaire (Ounces) - Adult
Time Frame: Study enrollment to six-month follow-up
Adult participants will complete a brief questionnaire to measure beverage intake (BEVQ-15).
Study enrollment to six-month follow-up
Food Behaviors as Assessed by the Townsend Food Behaviors Checklist (units on a scale) - Adult
Time Frame: Study enrollment to six-month follow-up
Adult participants will complete the Townsend Food Behaviors Checklist regarding consumption of foods and healthy food-related behaviors.
Study enrollment to six-month follow-up
Fruit and Vegetable Intake as Assessed by The Veggie Meter Score
Time Frame: Study enrollment to six-month follow-up
A Veggie Meter score (objective measure of fruit and vegetable intake) will be obtained for adults.
Study enrollment to six-month follow-up
Home Food Environment as Assessed by a Food Inventory Checklist (units on a scale)
Time Frame: Study enrollment to six-month follow-up
Adults will complete a self-report survey of the home food environment using the 23-item Home Food Inventory checklist.
Study enrollment to six-month follow-up
HbA1c - adult and child
Time Frame: Study enrollment to six-month follow-up
Child and adult HbA1c trained research staff will conduct finger sticks using established protocols (detailed protocol in Protection of Human Subjects)
Study enrollment to six-month follow-up

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Akilah Dulin, PhD, Brown University
  • Principal Investigator: Kim Gans, PhD, MPH, LDN, University of Connecticut

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)

April 12, 2023

Primary Completion (Actual)

January 12, 2025

Study Completion (Actual)

June 18, 2025

Study Registration Dates

First Submitted

March 21, 2023

First Submitted That Met QC Criteria

April 5, 2023

First Posted (Actual)

April 18, 2023

Study Record Updates

Last Update Posted (Actual)

May 18, 2026

Last Update Submitted That Met QC Criteria

May 14, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • 2022003499
  • 1R01DK128197-01A1 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

IPD will not be made available to outside individuals because the data obtained from this feasibility R01 will be used to inform a larger, fully-powered R01-equivalent clinical trial.

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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