ClinicalTrials.Veeva

Menu

A Digital Intervention to Promote Preschool Nutrition and Activity: The eHEROs Study

C

Cornell University

Status

Not yet enrolling

Conditions

Health Behavior

Treatments

Behavioral: KnowHow Program

Study type

Interventional

Funder types

Other
Other U.S. Federal agency

Identifiers

NCT07224412
IRB0010703
2021-68015-34557 (Other Grant/Funding Number)

Details and patient eligibility

About

The purpose of this pilot study is to assess the feasibility and acceptability of the Know-How program, a 10-week digital intervention for families of young children promoting healthy eating and activity behaviors and environments.

Full description

The purpose of this pilot study is to assess the feasibility and acceptability of the KnowHow program, a 10-week digital intervention for families of young children promoting healthy eating and activity behaviors and environments. The KnowHow program, which provides parent education on the topics of mindful parenting, healthy eating, and physical literacy, consists of three components: 1) a custom mobile application (app), 2) virtual group discussions, and 3) child-centered support materials mailed to participating families. The study will include an intervention group and a delayed control group. Feasibility of the digital intervention will be assessed at post-test only by recruitment, retention, usability, and acceptability. Implementation outcomes include measures of digital engagement, enactment, and intention to sustain, and will be collected at post-test only. Theoretical mediators include parent self-efficacy and behavioral capability and will be collected pre- and post-test. Behavioral outcomes, also collected at pre- and post-test, include mindful parenting, parent-child feeding practices, and physical activity parenting practices. Study assessments for the theoretical mediators and behavioral outcomes will be collected at Baseline (Time 1, pre-intervention) and at Post-Test (Time 2, post-intervention) at the same time for both groups. No additional assessments will be collected for the delayed control group at the conclusion of implementation.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Participants must have a preschool-aged child (3-5 years) with no disabilities or conditions that impact typical eating and activity behaviors.
  • Adult participants must have access to a smartphone, reliable internet at home, and can make video calls.

Exclusion criteria

  • Adults who do not have a child aged 3-5 or child has a disability/condition that impact typical eating and activity behaviors.
  • Technology access is limited.
  • Adults who read, write or speak a language other than English.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

KnowHow Program
Experimental group
Description:
Families will participate in the 10-week KnowHow program and will receive/participate in 1) a custom mobile application (app), 2) virtual group discussions, and 3) child-centered support materials
Treatment:
Behavioral: KnowHow Program
Wait List
No Intervention group
Description:
Families will not receive any intervention during the 10-week study. Families will receive access to the KnowHow app only for 10 weeks at the conclusion of the study.

Trial documents
1

Trial contacts and locations

1

Loading...

Central trial contact

Laura L Bellows, PhD, MPH, RDN

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems