search
Back to results

Health4Kids Intervention Trial for Hispanic Families (H4K)

Primary Purpose

Pediatric Obesity

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
behavioral counseling
Education Materials
Face to face counseling session
Text messages
Telephone Counseling
Newsletters
Sponsored by
The University of Texas Health Science Center at San Antonio
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pediatric Obesity focused on measuring Hispanic, overweight, families, pediatric, primary care

Eligibility Criteria

6 Years - 11 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • A child is eligible for the POM trial for meeting the following criteria:

    • identified by parent or legal guardian as Hispanic
    • age 6-11
    • overweight or obese (BMI between the 85th and 99.9thth (<99th) percentile for age and gender
    • one parent/guardian that the child resides with full-time must agree to participate in intervention and evaluation activities.

Exclusion Criteria:

  • A child will be excluded if he/she has:

    • a mental, emotional, or physical handicap identified by parents or health care provider that may interfere with study participation
    • a diagnosis of cardiovascular, pulmonary, or digestive disease
    • parent without a cell phone
    • parent unable or not willing to receive text messages
    • child or parent planning to move from the local area within the time span of the study.

Sites / Locations

  • University of Texas Health Science Center San Antonio

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard Care

Pediatric Obesity Management

Arm Description

Brief patient-centered behavioral counseling using the Healthy Lifestyle Prescription, health education materials and a community resource guide. Follow-up visits scheduled at 1, 6, and 12 months. Parent receives weekly general health education cell phone text messages for 12 months

All elements of standard care plus a family-based face to face counseling session with a health educator, telephone counseling, mailed newsletters and regularly scheduled cell phone text messages with tips and motivational messages for healthy eating and PA, as well as information on community events and resources.

Outcomes

Primary Outcome Measures

Change from baseline in weight (kg)
Weight will be measured using a portable Tanita Body Composition Analyzer SC-331S following standard protocol.
Change from baseline in waist circumference (cm)
Waist circumference (minimum waist girth) will be measured to the nearest 0.1 cm using a Myotape tape measure at the midpoint between the right iliac crests and the lower ribs when the subject is standing erect with feet together
Change from baseline in body mass index (BMI z score)
BMI will be calculated as weight (kg)/height squared (m2). Weight will be measured by bioelectrical impedance analysis (BIA) using the foot-to-foot pressure contact electrode BIA technique using a portable Tanita Body Composition Analyzer SC-331S following standard protocol. Height will be measured to the nearest 0.1 inch using a SECA brand stadiometer.

Secondary Outcome Measures

Change from baseline in fasting insulin (µIu/mL)
Fasting samples of serum will be drawn by a phlebotomist and processed by a commercial laboratory.
Change from baseline in fasting glucose (mg/dL)
Fasting samples of serum will be drawn by a phlebotomist and processed by a commercial laboratory.
Change in cholesterol (lipid panel: fasting total cholesterol, HDL cholesterol, LDL cholesterol and triglycerides) from baseline (mg/dL)
Fasting samples of serum will be drawn by a phlebotomist and processed by a commercial laboratory.
Change from baseline in moderate-to-vigorous physical activity (minutes/week)
Minutes per week of MVPA is assessed using accelerometry.
Change from baseline in consumption of sugar-sweetened beverages (servings/week)
Sugar-sweetened beverage consumption is assessed using the Block Kids Food Screener (Last Week version).
Change from baseline in consumption of fruits and vegetables (servings/day)
Fruit and vegetable consumption is assessed using the Block Kids Food Screener (Last Week version).

Full Information

First Posted
January 6, 2015
Last Updated
December 17, 2020
Sponsor
The University of Texas Health Science Center at San Antonio
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), The University of Texas at San Antonio, Bexar County Hospital District DBA University Health System
search

1. Study Identification

Unique Protocol Identification Number
NCT02343367
Brief Title
Health4Kids Intervention Trial for Hispanic Families
Acronym
H4K
Official Title
Pediatric Obesity Management Intervention Trial for Hispanic Families
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Completed
Study Start Date
January 2015 (undefined)
Primary Completion Date
November 19, 2019 (Actual)
Study Completion Date
March 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Texas Health Science Center at San Antonio
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), The University of Texas at San Antonio, Bexar County Hospital District DBA University Health System

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The H4K Trial is a randomized controlled trial to improve children's body composition by testing a comprehensive, culturally and linguistically relevant, family-oriented intervention for overweight and obese Hispanic children (ages 6-11) in three pediatric clinics in San Antonio, Texas. The H4K trial will test the efficacy of a 6-month pediatric obesity management intervention (physician counseling plus telephone counseling, newsletters and text messages) compared to standard care (physician counseling only) on three outcomes: 1) body composition (i.e., waist circumference, weight and z-BMI); 2) insulin, glucose and cholesterol levels; and 3) behavior change in physical activity (PA), sedentary behavior and consumption of sugary beverages and fruits and vegetables. The investigators will recruit 230 overweight and obese children-and a parent or guardian for each-and randomize them to the H4K intervention (n = 115 child/parent dyads) or standard care (n = 115 child/parent dyads). The investigators hypothesize that intervention children will significantly improve their body composition, increased their PA levels and diet quality (more fruits and vegetables and less sugary beverages), and decrease their sedentary activity, compared to children in standard care. If successful, this study will generate new scientific knowledge about effective Hispanic family-based approaches for obesity prevention with high potential for replication in underserved areas across the nation.
Detailed Description
Given the continuing rise of the U.S. Hispanic population, reversing the Hispanic childhood obesity epidemic is critical to the nation's future health. Mexican American children and those from socioeconomically disadvantaged families often are far more overweight and obese than their peers, heightening their risk for obesity-related health complications. Our proposed randomized controlled trial, the Health4Kids (H4K) Trial for Hispanic Families, aims to improve Hispanic children's body composition by testing a comprehensive, culturally and linguistically relevant, family-oriented intervention for overweight and obese (body mass index (BMI) between the 85th and 99.9thth (<99th) percentile for age and gender) Hispanic children ages 6-11 in pediatric clinics in San Antonio, Texas, a largely Hispanic city. Our team, formed during our pilot research funded by the Centers for Medicare and Medicaid Services (1H0CMS030457), unites academic investigators and community partners with experience working together to conduct behavioral and clinical interventions and outreach with Hispanics. The H4K trial will test the efficacy of a 6-month pediatric obesity management intervention (physician counseling plus telephone counseling, newsletters and text messages) compared to standard care (physician counseling only) on three outcomes: 1) body composition (i.e., waist circumference, weight and z-BMI); 2) insulin, glucose and cholesterol levels; and 3) behavior change in physical activity (PA), sedentary behavior and consumption of sugary beverages and fruits and vegetables. We will recruit 230 overweight and obese children-and a parent or guardian for each-and randomize them to the POM intervention (n = 115 child/parent dyads) or standard care (n = 115 child/parent dyads). From a baseline, we will measure the impact of the trial on the primary outcome (body composition) and secondary outcomes (insulin, glucose and cholesterol levels and several specific health behavior changes) at 1 month, 6 and 12 months post-randomization. We also will evaluate the critical role of parenting strategies and changes in the home environment as mediators of intervention effects. We hypothesize that intervention children will significantly improve their body composition, increased their PA levels and diet quality (more fruits and vegetables and less sugary beverages), and decrease their sedentary activity, compared to children in standard care. If successful, this study will generate new scientific knowledge about effective Hispanic family-based approaches for obesity prevention with high potential for replication in underserved areas across the nation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pediatric Obesity
Keywords
Hispanic, overweight, families, pediatric, primary care

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Care ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
518 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard Care
Arm Type
Active Comparator
Arm Description
Brief patient-centered behavioral counseling using the Healthy Lifestyle Prescription, health education materials and a community resource guide. Follow-up visits scheduled at 1, 6, and 12 months. Parent receives weekly general health education cell phone text messages for 12 months
Arm Title
Pediatric Obesity Management
Arm Type
Experimental
Arm Description
All elements of standard care plus a family-based face to face counseling session with a health educator, telephone counseling, mailed newsletters and regularly scheduled cell phone text messages with tips and motivational messages for healthy eating and PA, as well as information on community events and resources.
Intervention Type
Behavioral
Intervention Name(s)
behavioral counseling
Intervention Description
Pediatrician trained in motivational interviewing techniques provides brief lifestyle behavioral counseling to child and parent using a Healthy Lifestyle Prescription
Intervention Type
Other
Intervention Name(s)
Education Materials
Intervention Description
Health education materials about healthy eating and physical activity and a community resource guide
Intervention Type
Behavioral
Intervention Name(s)
Face to face counseling session
Intervention Description
30 minute face-to-face family-centered behavioral counseling session delivered by a health educator
Intervention Type
Behavioral
Intervention Name(s)
Text messages
Other Intervention Name(s)
SMS
Intervention Description
regularly scheduled cell phone text messages for 12 months
Intervention Type
Behavioral
Intervention Name(s)
Telephone Counseling
Intervention Description
14 telephone counseling sessions delivered by a health educator using motivational interviewing techniques. Two sessions per month for the first two months followed by one session per month for 10 months
Intervention Type
Behavioral
Intervention Name(s)
Newsletters
Intervention Description
12 monthly newsletters mailed to participant homes
Primary Outcome Measure Information:
Title
Change from baseline in weight (kg)
Description
Weight will be measured using a portable Tanita Body Composition Analyzer SC-331S following standard protocol.
Time Frame
6 months
Title
Change from baseline in waist circumference (cm)
Description
Waist circumference (minimum waist girth) will be measured to the nearest 0.1 cm using a Myotape tape measure at the midpoint between the right iliac crests and the lower ribs when the subject is standing erect with feet together
Time Frame
6 months
Title
Change from baseline in body mass index (BMI z score)
Description
BMI will be calculated as weight (kg)/height squared (m2). Weight will be measured by bioelectrical impedance analysis (BIA) using the foot-to-foot pressure contact electrode BIA technique using a portable Tanita Body Composition Analyzer SC-331S following standard protocol. Height will be measured to the nearest 0.1 inch using a SECA brand stadiometer.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Change from baseline in fasting insulin (µIu/mL)
Description
Fasting samples of serum will be drawn by a phlebotomist and processed by a commercial laboratory.
Time Frame
6 months
Title
Change from baseline in fasting glucose (mg/dL)
Description
Fasting samples of serum will be drawn by a phlebotomist and processed by a commercial laboratory.
Time Frame
6 months
Title
Change in cholesterol (lipid panel: fasting total cholesterol, HDL cholesterol, LDL cholesterol and triglycerides) from baseline (mg/dL)
Description
Fasting samples of serum will be drawn by a phlebotomist and processed by a commercial laboratory.
Time Frame
6 months
Title
Change from baseline in moderate-to-vigorous physical activity (minutes/week)
Description
Minutes per week of MVPA is assessed using accelerometry.
Time Frame
6 months
Title
Change from baseline in consumption of sugar-sweetened beverages (servings/week)
Description
Sugar-sweetened beverage consumption is assessed using the Block Kids Food Screener (Last Week version).
Time Frame
6 months
Title
Change from baseline in consumption of fruits and vegetables (servings/day)
Description
Fruit and vegetable consumption is assessed using the Block Kids Food Screener (Last Week version).
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
11 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A child is eligible for the POM trial for meeting the following criteria: identified by parent or legal guardian as Hispanic age 6-11 overweight or obese (BMI between the 85th and 99.9thth (<99th) percentile for age and gender one parent/guardian that the child resides with full-time must agree to participate in intervention and evaluation activities. Exclusion Criteria: A child will be excluded if he/she has: a mental, emotional, or physical handicap identified by parents or health care provider that may interfere with study participation a diagnosis of cardiovascular, pulmonary, or digestive disease parent without a cell phone parent unable or not willing to receive text messages child or parent planning to move from the local area within the time span of the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Deborah M Parra-Medina, PhD
Organizational Affiliation
UT Health San Antonio
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas Health Science Center San Antonio
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78229
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Health4Kids Intervention Trial for Hispanic Families

We'll reach out to this number within 24 hrs