BOUNCE to Health: A Healthy Lifestyle Program

Sponsor
University of Houston (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03925012
Collaborator
United Health Foundation (Other)
720
1
1
78
9.2

Study Details

Study Description

Brief Summary

The primary purpose of the BOUNCE study is to assess the effectiveness of a four-week family-based healthy lifestyle summer program in reducing adiposity indicators in Hispanic and African American girls and boys (ages 9-14 years old).

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Intervention
N/A

Detailed Description

The secondary aims of this study are to examine post-intervention changes in eating patterns, body image disturbances, unhealthy weight control practices, and fitness levels.

The investigators hypothesize that at the post-BOUNCE summer intervention, children will exhibit significant decreases in adiposity indicators (percent body fat and waist circumference), sweetened drinks and fried foods consumption, and an increase in physical fitness (aerobic capacity and minutes of moderated-vigorous physical activity) when compared to their baseline values after controlling for demographic, acculturation characteristics.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
720 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
BOUNCE to Health: A Healthy Lifestyle Program
Actual Study Start Date :
Jun 1, 2016
Anticipated Primary Completion Date :
Aug 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

Child participants will attend the healthy lifestyle summer program for 4 weeks, five days per week. The summer intervention will include daily one-hour nutrition education, one-hour behavioral counseling, and 3 one-hour exercise sessions. These physical activities include flexibility, games, traditional fitness, and dancing. Counseling and school psychology students, registered dietitian/nutrition educators, and fitness specialists will lead the respective sessions. Parental guardians will participate in a two-hour weekly parental sessions that involve: 1)nutrition education with cooking demonstrations of healthy recipes; 2)behavioral counseling to learn effective parenting strategies on how to support their child's healthy nutrition and exercise habits and goals; and 3)exercise sessions where parents will engage in different physical activities and will receive fitness tips on how to promote an active lifestyle for the entire family.

Behavioral: Intervention

Outcome Measures

Primary Outcome Measures

  1. Change in Percent Body Fat [pre & post intervention at Week 4]

    percent body fat obtained from a foot-to-foot bio-electrical impedance assessment

  2. Anthropometric Change in Abdominal Fat [pre & post intervention at Week 4]

    assessed through waist circumference (WC) measurements following guidelines from National Health and Nutrition Examination

  3. Anthropometric Change in Hip Circumference [pre & post intervention at Week 4]

    hip circumference (HC) measurements following guidelines from National Health and Nutrition Examination (for parents only)

Secondary Outcome Measures

  1. Physical Activity [pre & post intervention at Week 4]

    Motion analyzer measures the percentage of youth who meet 60 minutes of daily moderate-to-vigorous physical activity per week

  2. Sweetened Drinks [pre & post intervention at Week 4]

    self-report measure

  3. Fried Food Consumption [pre & post intervention at Week 4]

    self-report measure

Eligibility Criteria

Criteria

Ages Eligible for Study:
9 Years to 14 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Both parental guardians (mother and father) and target child must be of Hispanic or African American descent

  • Child must be between the ages of 9-14 years

  • Child must be overweight/obese as defined by a body mass index percentile for age- gender specific between the 85th-100th percentile

  • Child must have no physical disability or medical conditions that interfere with their participation in an exercise program

  • Children must have no extensive diet restrictions that would hinder their participation in the BOUNCE nutrition component (e.g., unable to eat solid foods)

  • All children will be required to submit evidence of a medical examination conducted by a health professional

  • Parental guardians and child must be available to participate for the duration of the BOUNCE summer

Exclusion Criteria:
  • Child and parental guardians are not Hispanic or African American

  • Child is not between the ages of 9-14 years

  • Child is underweight or normal weight (BMI < 85 percentile) or are morbidly obese (BMI

100 percentile)

  • Child or mother are pregnant or physically unable to participate

  • Child has extensive diet restrictions that would hinder their participation in the BOUNCE nutrition component (e.g., unable to eat solid foods)

  • Child does not have submitted evidence of a medical examination conducted by a health professional

Note: We will encourage both maternal and paternal guardians to participate in the measurements and interventions. However, if the paternal guardian refuses to participate or there is no father figure present in the family, maternal guardian-child pairs will be still eligible to participate in this study. If the children are of mixed race, but identify themselves as Hispanic or African American and at least one of their parents is either Hispanic or African American, they will be still eligible to participate.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Houston Houston Texas United States 77204

Sponsors and Collaborators

  • University of Houston
  • United Health Foundation

Investigators

  • Principal Investigator: Norma Olvera, PhD, University of Houston

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Norma Olvera, Principal Investigator, University of Houston
ClinicalTrials.gov Identifier:
NCT03925012
Other Study ID Numbers:
  • 16447-01
First Posted:
Apr 23, 2019
Last Update Posted:
May 1, 2019
Last Verified:
Apr 1, 2019
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 May 1, 2019