search
Back to results

Míranos! Program, a Preschool Obesity Prevention RCT

Primary Purpose

Obesity, Healthy Eating, Physical Activity

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Center-based Intervention
Home-based Intervention
Active Control
Sponsored by
The University of Texas at San Antonio
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Obesity

Eligibility Criteria

3 Years - 5 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • The child must be enrolled in a full-day Head Start center
  • The child must be 3 years old at baseline, one child per family, parental consent

Exclusion Criteria:

  • N/A

Sites / Locations

  • University of Texas at San Antonio

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Center-based intervention

Center-and-home-based intervention

Active Control

Arm Description

In-person, child-focused intervention taking place only at the Head Start centers

In-person, child-focused intervention taking place only at the Head Start centers. Delivered in-person at Head Start centers and the family home.

Active comparison group

Outcomes

Primary Outcome Measures

Change in Body Mass Index
Child's height and weight will be measured twice with no shoes and light clothing in an area separated by a privacy screen, using a stadiometer and digital weight scale. Discrepancy between the two measures must be ≤0.2 cm and≤ 0.10 kg. BMI, BMI-percentile, and zBMI for age and gender will be calculated using the average of the two measures based CDC Growth Charts.

Secondary Outcome Measures

Change in Physical Activity, Sedentary Activity, and Sleep
7-d accelerometry to measure the minutes of light-, moderate- and vigorous-intensity physical activity, sedentary activity, and sleep/day
Change in Parent report of screen time and sleep
7-d parent log to track time that child spends watching TV/DVD and sleeping each day
Change in Fruit, vegetable, and beverage consumption
Assessment of children's consumption of fruits, vegetables and beverages by screener on the frequency and portion size of food items that will be completed by the parents as well as aggregate plate waste to asses intake at sites.
Change in Food preference
A computer-assisted pictorial test to measure young children's preferences for healthy food
Change in Parent Behavior
Parents will complete: 1) the Home Health Environment survey, 2) the Parenting Strategies for Eating and Activity Scale, 3) health knowledge assessment; and 4) parental confidence/self-efficacy scale.
Demographic Information
Information will be collected from the parents on family socioeconomic status (parent education, income, employment, health insurance, food insecurity, race/ethnicity, age, sex), acculturation (a 12-item bidirectional measure), family structure, type of residence, and family health history at baseline.

Full Information

First Posted
June 27, 2018
Last Updated
February 4, 2020
Sponsor
The University of Texas at San Antonio
Collaborators
University of Texas at Austin, University of Maryland, College Park, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Family Service Association of San Antonio Inc., Parent/Child Incorporated (PCI) of San Antonio and Bexar County
search

1. Study Identification

Unique Protocol Identification Number
NCT03590834
Brief Title
Míranos! Program, a Preschool Obesity Prevention RCT
Official Title
Obesity Prevention in Head Start: Míranos! Program
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2018 (Actual)
Primary Completion Date
August 2020 (Anticipated)
Study Completion Date
August 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Texas at San Antonio
Collaborators
University of Texas at Austin, University of Maryland, College Park, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), Family Service Association of San Antonio Inc., Parent/Child Incorporated (PCI) of San Antonio and Bexar County

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The prevalence of obesity remains high in American children aged 2-5 while one in three Head Start children is overweight or obese. The proposed study is designed to test the efficacy of an early childhood obesity prevention program which promotes healthy growth in predominantly Latino children in Head Start. The program is a group clustered randomized controlled trial in partnership with two local Head Start organizations to address key enablers and barriers in obesity prevention in young children. The study has three specific aims: To test the efficacy of the Miranos! intervention on healthy weight growth (primary outcome) in normal weight, overweight, and obese children. To test the impact of the Miranos! intervention on children's physical activity, sedentary behavior, sleep, and dietary behaviors (secondary outcomes). To evaluate cost-effectiveness of the Miranos! intervention. Miranos! will be delivered in Fall and Spring (8 months) and followed by a summer health campaign.
Detailed Description
Using a three-arm design, 12 Head Start (HS) centers in equal number will be randomly assigned to one of three conditions: 1) a combined center- and home-based intervention, 2) center-based intervention only, or 3) active control. The interventions will be delivered during the academic year (an 8-month [mo] period). A total of 525 3-year-old children (52% females; in two cohorts) will be enrolled in the study at baseline and followed prospectively one-year post-intervention. The first cohort will be recruited in summer 2018. The second cohort will be recruited in summer 2019. Data collection will be conducted at baseline (T0), immediate post-intervention (T1), and 1-year post-intervention follow-up (T2) and include children's height, weight, accelerometry-based PA and sedentary behavior, TV watching and sleep by parent reports, gross motor development, dietary intakes, food preference. Information on family background, parental PA- and nutrition-related practices, parental weight and health behaviors, PA and nutrition policies and environments at the center and home, and costs associated with intervention delivery will be collected. The primary endpoint for the study is the BMI at the posttest immediately following the completion of the intervention (T1). Recruitment: Participant recruitment will take place during summer by sending a recruitment packet to child's home. This packet includes: study information sheet, recruitment flyer, informed consent form, a letter from center director and study PIs. Process Evaluation: The process evaluation is informed by the NIH Behavior Change Consortium Treatment Fidelity Workgroup's best practice recommendations and recent multi-component RCTs. Míranos! has multiple components with multiple activities, the investigators will use many indicators to evaluate the fidelity and completeness of the implementation of all components and determine contribution of each component by linking it to the primary and secondary outcomes. The investigators will collect both quantitative/qualitative data to assess cross-site treatment consistency, non-treatment-related effects, and document protocol changes. First, intervention dose delivered will be measured by: 1) pre-/post-study center environmental assessment by the Environment and Policy Assessment and Observations (EPAO) and auditing of meal menus; 2) completion of delivery schedule of staff, peer leader training, parent education sessions, home visits; 3) evaluation of staff, peer leader training; 4) monthly auditing of weekly lesson plans; and 5) monthly checklist of use of Míranos! Activity Cards, children's story books, HHL learning activities. Second, the intervention dose received will be assessed by: 1) attendance records of staff, peer leader training, parent education sessions; 2) certification test of staff, peer leader training; 3) monthly staff evaluation (rating scale) of children's learning of HHL content, gross motor skills, eating behaviors; 4) post-study parent intercept interviews; and 5) post-study focus groups on program delivery process with staff (n=24) and parents (n=32). Third, participants' responses to the intervention will be evaluated by: 1) random observations of staff behavior (rating scale) during outdoor play and lunch by research staff; 2) assessments on children's PA by the System for Observing Fitness Instruction Time for Preschoolers and diet by group plate waste test in 3 randomly selected centers; 3) in-depth interviews with staff (n=48) for program feedback; and 4) post-study staff and parent evaluation (rating scale) of satisfaction with intervention components/activities.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Obesity, Healthy Eating, Physical Activity, Health Knowledge, Attitudes, Practice, Gross Motor Development

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
The parents of the children were informed that their Head Start center will be randomly assigned to one of the three study groups.
Allocation
Randomized
Enrollment
525 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Center-based intervention
Arm Type
Experimental
Arm Description
In-person, child-focused intervention taking place only at the Head Start centers
Arm Title
Center-and-home-based intervention
Arm Type
Experimental
Arm Description
In-person, child-focused intervention taking place only at the Head Start centers. Delivered in-person at Head Start centers and the family home.
Arm Title
Active Control
Arm Type
Active Comparator
Arm Description
Active comparison group
Intervention Type
Behavioral
Intervention Name(s)
Center-based Intervention
Other Intervention Name(s)
CBI
Intervention Description
Center nutrition and physical activity policy modification to increase fruit and vegetable servings and more physical activity throughout the day Staff training and technical assistance Health education on healthy habits (diet, physical activity, sleep, screen time) using the Sesame Workshop Healthy Habits for Life (HHL) resource kit Health contests Gross motor and physical activity program Miranos! activity cards based on children storybooks
Intervention Type
Behavioral
Intervention Name(s)
Home-based Intervention
Other Intervention Name(s)
C+HBI
Intervention Description
Monthly interactive poster education sessions led by parent peer educators during child pick-up time. Held at Head Start Center. These sessions include family health challenges and take-home activities. Three Home Visits delivered by Head Start staff. Obesity prevention goal-setting integrated into existing Head Start home visits 16 semi-monthly, Family Newsletters with stories, tips, and strategies to promote healthy habits for preschool children Incorporating activities related to PA, nutrition and sleep into existing Head Start Center Summer Calendars
Intervention Type
Behavioral
Intervention Name(s)
Active Control
Intervention Description
Children will receive Head-Start-approved health education program for children: "I Am Moving, I Am Learning". In addition, the investigators will deliver an early childhood literacy program to all active control children to increase buy-in and retention.
Primary Outcome Measure Information:
Title
Change in Body Mass Index
Description
Child's height and weight will be measured twice with no shoes and light clothing in an area separated by a privacy screen, using a stadiometer and digital weight scale. Discrepancy between the two measures must be ≤0.2 cm and≤ 0.10 kg. BMI, BMI-percentile, and zBMI for age and gender will be calculated using the average of the two measures based CDC Growth Charts.
Time Frame
Baseline, 8 months, 21 months
Secondary Outcome Measure Information:
Title
Change in Physical Activity, Sedentary Activity, and Sleep
Description
7-d accelerometry to measure the minutes of light-, moderate- and vigorous-intensity physical activity, sedentary activity, and sleep/day
Time Frame
Baseline, 8 months, 21 months
Title
Change in Parent report of screen time and sleep
Description
7-d parent log to track time that child spends watching TV/DVD and sleeping each day
Time Frame
Baseline, 8 months, 21 months
Title
Change in Fruit, vegetable, and beverage consumption
Description
Assessment of children's consumption of fruits, vegetables and beverages by screener on the frequency and portion size of food items that will be completed by the parents as well as aggregate plate waste to asses intake at sites.
Time Frame
Baseline, 8 months, 21 months
Title
Change in Food preference
Description
A computer-assisted pictorial test to measure young children's preferences for healthy food
Time Frame
Baseline, 8 months, 21 months
Title
Change in Parent Behavior
Description
Parents will complete: 1) the Home Health Environment survey, 2) the Parenting Strategies for Eating and Activity Scale, 3) health knowledge assessment; and 4) parental confidence/self-efficacy scale.
Time Frame
Baseline, 8 months, 21 months
Title
Demographic Information
Description
Information will be collected from the parents on family socioeconomic status (parent education, income, employment, health insurance, food insecurity, race/ethnicity, age, sex), acculturation (a 12-item bidirectional measure), family structure, type of residence, and family health history at baseline.
Time Frame
Baseline

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: The child must be enrolled in a full-day Head Start center The child must be 3 years old at baseline, one child per family, parental consent Exclusion Criteria: N/A
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zenong Yin, PhD
Organizational Affiliation
University of Texas at San Antonio
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Deborah Parra-Medina, PhD
Organizational Affiliation
University of Texas at Austin
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Texas at San Antonio
City
San Antonio
State/Province
Texas
ZIP/Postal Code
78249
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All IPD collected will be shared
IPD Sharing Time Frame
Data will become available after data has been analyzed for primary and secondary outcome measures
IPD Sharing Access Criteria
Data will be made available for research educational purposes.
Citations:
PubMed Identifier
31179916
Citation
Yin Z, Ullevig SL, Sosa E, Liang Y, Olmstead T, Howard JT, Errisuriz VL, Estrada VM, Martinez CE, He M, Small S, Schoenmakers C, Parra-Medina D. Study protocol for a cluster randomized controlled trial to test " inverted exclamation markMiranos! Look at Us, We Are Healthy!" - an early childhood obesity prevention program. BMC Pediatr. 2019 Jun 10;19(1):190. doi: 10.1186/s12887-019-1541-4.
Results Reference
derived

Learn more about this trial

Míranos! Program, a Preschool Obesity Prevention RCT

We'll reach out to this number within 24 hrs