N/A
N=42
Buen Provecho!: A Virtual Family-Based Intervention to Promote Health
Health Behavior · Diet, Healthy · Childhood Obesity
Bottom Line
View on ClinicalTrials.gov: NCT05419557 ↗Enrolled (actual)
42
Serious AEs
0.0%
Results posted
Oct 2024
Primary outcome: Primary: Count of Participants Who Consumed Vegetables With Their Dinner Meal More Than 5 Days Per Week — 9; 5 Participants — p=0.02
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Virtual Family-Based Healthy Plate Club (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Inova Health Care Services
- Primary completion
- Jan 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Count of Participants Who Consumed Vegetables With Their Dinner Meal More Than 5 Days Per Week |
9; 5 | 0.02 sig |
| PRIMARY Count of Guardians Who Reported Being Confident or Very Confident That They Could Increase the Number of Vegetables the Child Eats Each Week |
7; 5 | 0.015 sig |
Summary
The purpose of this pilot study is to compare the effectiveness of an expanded virtual educational program at modifying knowledge, self-efficacy, and behaviors when compared to traditional in-office counseling for guardians of children who are obese or overweight.
Eligibility Criteria
Inclusion Criteria
Inclusion criteria include:
- Child is clients at community clinic
- Child between the ages 6-12 years
- Child has a BMI percentage greater than 85%
- Primary parent or guardian is > 18 years of age
- Family identifies as Hispanic and Spanish is one of the primary languages spoken in the home
- Children will be living with the primary guardian or parent for the duration of the program
- Access to the internet
- Parent or guardian is willing to commit to engaging in the 12 week program
Exclusion Criteria
- Family plans to change location within the year
- During initial screening for the study, the study PI determines that the intervention may exacerbate existing medical conditions of the child or the family.
Data sourced from ClinicalTrials.gov (NCT05419557). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.