Combining Prebiotic and Diet/Physical Activity Educational Program Effects on Body Composition and Intestinal Microbiota in Children

Sponsor
Marquette University (Other)
Overall Status
Completed
CT.gov ID
NCT05671731
Collaborator
Medical College of Wisconsin (Other)
123
2
4.9

Study Details

Study Description

Brief Summary

The purpose of this study was to determine the feasibility, acceptability, and initial efficacy of combining prebiotic (Beneo Synergy 1) and calcium treatment with Project FUN (an online nutrition and physical activity program) on body composition and intestinal microbiota among 4th and 5th grade children whose social determinants placed them at higher risk for obesity. This aim was addressed through testing the following hypotheses:

H1 Prebiotic and calcium supplementation in combination with Project FUN, will result in improved body composition scores, dietary fat percentage, and physical activity compared to a usual class control who did not receive the intervention.

H2 Higher counts of Bacteroides and Bifidobacterium as well as fewer Firmicutes in the stool samples will correlate with improvement in body composition scores.

Since this was a pilot community-based efficacy study, the following feasibility, acceptability, and descriptive research questions were also addressed:

RQ1 What percentages of participants submit stool samples, body composition assessments and complete at least 70 percent of the intervention over the course of a 12-week study? RQ2 What is the relationship between changes in body composition scores, dietary fat percentage, physical activity and microbiota in stool samples before and after the 12-week intervention?

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Beneo Synergy 1
  • Behavioral: Project FUN
N/A

Detailed Description

The purpose of this study was to determine the feasibility, acceptability, and initial efficacy of combining prebiotic (Beneo Synergy 1) and calcium treatment with Project FUN (an online nutrition and physical activity program) on body composition and intestinal microbiota among 4th and 5th grade children whose social determinants placed them at higher risk for obesity. This aim was addressed through testing the following hypotheses:

H1 Prebiotic and calcium supplementation in combination with Project FUN, will result in improved body composition scores, dietary fat percentage, and physical activity compared to a usual class control who did not receive the intervention.

H2 Higher counts of Bacteroides and Bifidobacterium as well as fewer Firmicutes in the stool samples will correlate with improvement in body composition scores.

Since this was a pilot community-based efficacy study, the following feasibility, acceptability, and descriptive research questions were also addressed:

RQ1 What percentages of participants submit stool samples, body composition assessments and complete at least 70 percent of the intervention over the course of a 12-week study? RQ2 What is the relationship between changes in body composition scores, dietary fat percentage, physical activity and microbiota in stool samples before and after the 12-week intervention? The sample included 4th- 5th grade students at two private urban schools where 98% were eligible for free or reduced fee lunch. Of the 123 consenting 56% were male; 71% Latinx; 15% African American; 14% Other. Three percent were underweight; 49% normal weight; 22% overweight; 25% obese.

Consenting Latinx (n=20) and African American (n=8) participants completed microbiome analysis. Of these 54% were male; 6.5% underweight; 38.7% normal weight; 32.3% overweight; 2.6% obese.

Study Design

Study Type:
Interventional
Actual Enrollment :
123 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
cluster randomized controlled feasibility trialcluster randomized controlled feasibility trial
Masking:
Single (Outcomes Assessor)
Masking Description:
Research assistants collecting data did not know group assignment of participants.
Primary Purpose:
Prevention
Official Title:
The Effect of Combining Prebiotic Treatment With a Diet/Physical Activity Educational Program on Body Composition and Intestinal Microbiota in 4th and 5th Grade Children
Actual Study Start Date :
Nov 13, 2012
Actual Primary Completion Date :
Apr 11, 2013
Actual Study Completion Date :
Apr 11, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

The intervention group received Beneo Synergy 1 - 4gm twice/school day in 4 ounces orange juice with calcium for 12 weeks. We started with 1gm then increased the next day by a gram to reach the 4gm dose. Intervention group participants completed Project FUN (8 module online nutrition and physical activity program) individually (password protected) in the school computer lab along with a workbook also used to check intervention completion.

Dietary Supplement: Beneo Synergy 1
Other Names:
  • oligofructose enhanced inulin
  • Behavioral: Project FUN
    Project FUN, a culturally tailored online nutrition and physical activity program is based on the Health Promotion/ Transtheoretical Model. It includes 8 modules offered in a password-protected learning management system along with a workbook also used to assure intervention completion.

    No Intervention: Control

    The control group participated in usual school activities only completing pre and post measures.

    Outcome Measures

    Primary Outcome Measures

    1. Body mass index percentile mean change from baseline after 12 weeks [Pre and after 12-week intervention]

      Weights to the nearest tenth of a pound were collected using a Seca model 8761321004 scale. Heights in stocking feet were measured to the nearest hundredth of an inch with a stadiometer (Seca Model 213, Hanover, MD, USA). Body mass index percentile was calculated using the Centers for Disease Control and Prevention school algorithm including birth date, measurement date, height, and weight

    Secondary Outcome Measures

    1. Body fat percentage mean change from baseline after 12 weeks [Pre and after 12-week intervention]

      Measured with the Omron HBF-306C hand-held bioimpedance monitor

    2. Gut microbiota mean change from baseline after 12 weeks (Intervention group only) [Pre and after 12-week intervention]

      Genomic markers of stool samples were analyzed by Roche 454 pyrosequencing of fecal 16S rDNA and validated by quantitative polymerase chain reaction.

    Other Outcome Measures

    1. Dietary fat percentage mean change from baseline after 12 weeks [Pre and after 12-week intervention]

      A 21-item, five-option response format measure was used developed by Prochaska JJ, Sallis JF, Rupp J. Screening measure for assessing dietary fat intake among adolescents.

    2. Physical activity mean change from baseline after 12 weeks [Pre and after 12-week intervention]

      Prochaska JJ, Sallis JF, Long B. A physical activity screening measure for use with adolescents in primary care.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • 4th- 5th grade students at two private urban schools where 98% were eligible for free or reduced fee lunch.
    Exclusion Criteria:
    • Parents indicated their child had taken an antibiotic in the last month since antibiotics can change intestinal flora though none required exclusion for this reason or for illness preventing participation.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Marquette University
    • Medical College of Wisconsin

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Marquette University
    ClinicalTrials.gov Identifier:
    NCT05671731
    Other Study ID Numbers:
    • 2411
    First Posted:
    Jan 5, 2023
    Last Update Posted:
    Jan 5, 2023
    Last Verified:
    Dec 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
    Keywords provided by Marquette University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 5, 2023