Actively Recruiting

Phase Not Applicable
Age: 2Years +
All Genders
Healthy Volunteers
ID07046351

weSIPsmarter: An Adaptation and Efficacy Trial to Evaluate a Behaviorally Based Digital Health Intervention Aimed at Reducing Sugary Drinks Among Rural Head Start Preschoolers and Their Parents

Led by University of Virginia · Updated on 2025-12-16

744

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

U

University of Virginia

Lead Sponsor

N

National Cancer Institute (NCI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating a digital health program called weSIPsmarter to reduce sugary drink consumption among preschool-aged children and their parents in rural areas. The study focuses on families involved in rural Head Start programs in Appalachia and the southern Black Belt, aiming to improve health behaviors and prevent chronic conditions related to high sugary drink intake. This trial addresses a gap in interventions designed for rural communities and young children aged 2 to 5 years. The study randomly assigns 12 rural Head Start programs to either the weSIPsmarter intervention or a control group called weLearn2Read. The weSIPsmarter program includes interactive behavioral components such as self-monitoring of beverage intake and parenting practices, goal setting, a resource help line, and water vouchers for families concerned about tap water quality. Participants in this group complete six learning modules, track daily sugary drink consumption, and parents also record daily weight. The control group completes six educational modules focused on reading readiness and receives children's books and optional reminders. Participants, which are parent-child pairs from the Head Start programs, will be assessed at the start, after 9 weeks, and again at 12 months. Measurements include sugary drink intake, weight, height, body mass index, diet quality, and parent health literacy. Researchers will also study parent engagement, the program's reach, and how well it is adopted and maintained by the Head Start centers. Total participation spans over one year, with focus on both reducing sugary drink use and sustaining healthier behaviors over time.

CONDITIONS

Brief Title

weSIPsmarter: Evaluating a Digital Health Intervention Aimed at Reducing Sugary Drinks Among Rural Head Start Preschoolers and Their Parents

Who Can Participate

Age: 2Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Head Start sites must be located in or near a rural county (RUCC 4-9) within Appalachia or the Black Belt regions
  • Head Start sites must have an enrollment of 120 families or more and show commitment to the study
  • Children must be between 2 and 5 years old and enrolled in a participating Head Start
  • A legal guardian who can consent must enroll and consent for the child
  • Only one parent-child pair per household is eligible to participate
Not Eligible

You will not qualify if you...

  • Parents who participated in the formative research phase for this study under SBS 4522 are excluded

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 9 weeks

Participants engage in the assigned digital health intervention program targeting behavior change to reduce sugary drink intake. This includes completing six structured Cores, daily self-monitoring of sugary drink intake and parenting feeding practices, action planning, and access to support resources.

Daily self-monitoring and six core sessions over 9 weeks

Follow-up

Duration - Up to 12 months post-intervention

Participants complete assessments to evaluate the maintenance of reduced sugary drink consumption and other health outcomes 12 months after the intervention.

1 follow-up visit

Trial Site Locations

Total: 1 location

1

University of Virginia

Christiansburg, Virginia, United States, 24073

Actively Recruiting

Loading map...

Research Team

J

Jamie Zoellner, PhD RD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here