Buen Provecho!: A Virtual Family-Based Intervention to Promote Health

Sponsor
Inova Health Care Services (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05419557
Collaborator
(none)
50
2
12

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Virtual Family-Based Healthy Plate Club
N/A

Detailed Description

Rationale: Obesity rates are significantly higher among Hispanic youth in the United States, disproportionately putting these children at an increased risk for obesity-related diseases such as hypertension, dyslipidemia, and impaired glucose tolerance. While virtual programming offers an innovative option for pediatric weight management, limited data exists on the efficacy of virtual interventions for this population and their guardians (parents / caregivers).

Objectives: The purpose of this pilot study is to compare the effectiveness of an expanded virtual educational program (expanded -Inova Healthy Plate Club, x-IHPC) at modifying knowledge, self-efficacy, and behaviors when compared to traditional in-office counseling for guardians of children who are obese or overweight.

Study Design: In order to test the effectiveness of the x-IHPC intervention, outcomes from participants in this pilot study will be compared with outcomes from a comparison group of similar participants who receive standard nutrition counseling during their regularly scheduled check-ups. The team will enroll 25 children in the x-IHPC intervention and the same number in the comparison group (n=50). Both groups will receive standard in-office counseling, but the intervention group will also receive the x-IHPC.

Study Methodology: The comparison group receives standard, in-office counseling at visits 1, 3-months and 6-months. The intervention group receives standard in-office counseling at the same intervals, and also participates in a 12-week x-IHPC developed by a dietician curriculum specialist. In addition, a key pillar of this study is identifying and training Community Health Workers (CHWs) to be Spanish-speaking facilitators of the x-IHPC and utilizing community engagement strategies. Training these CHWs and including them in designing the x-IHPC curriculum, will ensure that the programming is culturally appropriate; includes local features that relate directly to the community's needs; and enables study facilitators to respond effectively to the questions and learning needs of the parents and children involved in the program.

Statistical Methodology:

To examine the research question, a longitudinal analysis using generalized estimating equations (GEE) will be conducted to assess if mean differences exist on dietary measures, screen time, sleep quality, physical activity and guardian self-efficacy and confidence between the intervention and comparison groups while accounting for the correlation among the repeated measurements and controlling for covariates.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
concurrent groupsconcurrent groups
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Buen Provecho!: A Virtual Family-Based Intervention to Promote Health
Anticipated Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Sep 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Intervention

12 week virtual family-based health eating program

Behavioral: Virtual Family-Based Healthy Plate Club
IHPC provides produce boxes, nutrition and meal-preparation, education, and supportive counseling to address barriers related to obtaining produce and food. The intervention provides participants with a bi-weekly produce box for 12 weeks and helps families identify sustainable ways to obtain vegetables once the produce boxes end. The CHW will support families by coaching them on how to prepare these unfamiliar vegetables, give tips on finding sales at grocery stores, as well as by navigation to food assistance sites including food pantries. Parents will learn strategies to increase vegetable consumption by addressing perceived barriers - such as the child doesn't like vegetables. Curriculum will also include topics such as how to increase physical activity and reduce screen time.

No Intervention: Comparison

Standard in-office counseling about diet

Outcome Measures

Primary Outcome Measures

  1. NHANES food frequency questionnaire [3 months]

    measures food consumption and type

  2. Healthy Home Survey [3 months]

    screen time estimates and types

  3. Healthy Home Survey [3 months]

    physical activity questionnaire measures amount and type of physical activity

  4. Self-Efficacy scale [3 months]

    guardian self-efficacy and confidence questions related to modifiable lifestyle behaviors

Secondary Outcome Measures

  1. BMI [3 months]

    BMI

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
Inclusion criteria include:
  1. Both Guardian and Child are clients at community clinic

  2. Child between the ages 6-10 years

  3. Child has a BMI percentage greater than 85%

  4. Primary parent or guardian is > 18 years of age

  5. Family identifies as Hispanic and Spanish is one of the primary languages spoken in the home

  6. Children will be living with the primary guardian or parent for the duration of the program

  7. Access to the internet

  8. Parent or guardian is willing to commit to engaging in the 12 week program

Exclusion Criteria:
  1. Family plans to change location within the year

  2. During initial screening for the study, the study PI determines that the intervention may exacerbate existing medical conditions of the child or the family.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Inova Health Care Services

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Inova Health Care Services
ClinicalTrials.gov Identifier:
NCT05419557
Other Study ID Numbers:
  • U21-12-4630
First Posted:
Jun 15, 2022
Last Update Posted:
Jul 22, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 22, 2022