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Status unknownNCT03885115LUAMUpdated Apr 8, 2019

Lace Up and Move: Structured After School Intervention for Hispanic and African American Youth

An interventional study of Intervention in Childhood Obesity, Obesity and Physical Activity, sponsored by University of Houston. Status unknown at 1 site in United States. Open to participants aged 9 Years to 14 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-04-08.

Sponsored by University of Houston · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Apr 2019), so the status shown — last known as Active, not recruiting — may be out of date.

From the registry’s dates

  • Registered 1 year 3 months after the study started (first participant enrolled Nov 2017, registered Mar 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
600
Allocation
Randomized
Ages
9 Years to 14 Years
Sex
All
01

Study summary

The purpose of this study is to test the efficacy of Lace Up and Move (LUAM), a structured after-school exercise intervention, designed to increase moderate-to-vigorous physical activity (MVPA) and enhance sleep quality among Hispanic and African American (AA) boys and girls.

Read the detailed description

This study uses a randomized comparison-group pre-post-test design. Overall objectives of LUAM are to: (1) to increase the percentage of youth who meet 60 minutes of daily MVPA per week; (2) to improve the quality of sleep patterns (i.e., sleep efficiency and duration); and (3) to reduce percent body fat (%BF). It is hypothesized that compared to the control group (CG) participants, the experimental group (EG) participants will exhibit: (a) greater increase in percentage of children who meet 60 minutes of daily MVPA per week; (b) greater increase of sleep efficiency and duration; and (c) greater decrease in sleep latency and (d) greater decrease in %BF.

02

Conditions studied

  • Childhood Obesity
  • Obesity
  • Physical Activity
03

In context

Obesity

6,296 studies on the registry are indexed under Obesity; 1,695 are open to participants now.

This study's planned enrollment of 600 is above the median of 78 across 4,878 interventional studies indexed under Obesity.

Browse Obesity studies →

Lead sponsor

University of Houston is the lead sponsor of 101 studies on the registry; 17 are open to participants now.

Of its 9 completed or terminated interventional studies of FDA-regulated products, 3 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
9 Years to 14 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • child and at least their mother [or one member of the family] must be of Hispanic or African American descent
  • child must have no physical disability or medical conditions that interfere with their participation in the exercise program

Exclusion criteria

Exclusion Criteria:

  • neither child nor parental guardians is of Hispanic or African American descent
  • child is not between the ages of 9-14 years
  • child is pregnant or physically unable to participate in the exercise program.
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Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
600 participants (estimated)

Study arms

  • Experimental
    Intervention

    Participants randomly assigned to the experiential group (EG) will receive a 12-week structured exercise that will consist of two group fitness sessions (i.e. kickboxing, Zumba, fitness yoga, and other aerobic exercises) every week. Certified fitness instructors will lead each session and participants will learn strategies how to be more active during the daily routines at home. Parents or other relatives in the EG will participate in one 2-hour session every four weeks (total of 3 sessions) designed to help them support their children and entire family in being active and eat healthy at home. Parents will meet with a fitness instructor who will provide specific tips on how to increase physical activity at home as well as providing community resources to be active. A basic nutrition education and cooking demonstrations, and healthy recipes will be also provided to parents at these workshops. Data/assessments are collected, pre and post the 12 weeks intervention.

    Behavioral: Intervention

  • No intervention
    Control

    Participants randomly assigned to the control group (CG) will receive once a week recreational structured group play/game sessions led by trained BOUNCE interns/staff. The control group will receive 60 minute of structured free play sessions (i.e. recreational games) once a week for 12 weeks. Every 4 weeks, parents will be given (either sent home with their child or via email or mail) basic nutrition information, healthy recipes, and tips to promote physical activity at home as well as community resources to be active. Data/assessments are collected, pre and post the 12 weeks intervention.

Interventions

  • BehavioralIntervention

    Involves 12-weeks of education related to healthy behaviors, nutrition, and exercise from certified fitness instructors.

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What researchers measure

Primary outcomes

  1. Child Physical Activity

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

    Time frame: pre & post intervention at Week 12

Secondary outcomes

  1. Sleep

    assess using self-report survey

    Time frame: pre & post intervention at Week 12

  2. Sleep Quality

    assess quality of sleep patterns using a small motion analyzer that measures sleep efficiency, duration and latency

    Time frame: pre & post intervention at Week 12

  3. Body fat percentage

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

    Time frame: pre & post intervention at Week 12

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Study locations

1 site
  • University of Houston
    Houston, Texas 77204, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 8, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03885115
Lead sponsor
University of Houston
Collaborators
United Health Foundation
Responsible party
Norma Olvera (Principal Investigator, University of Houston) — Principal investigator
First posted
Mar 21, 2019
Start date
Nov 28, 2017
Primary completion
Dec 2019 (estimated)
Completion
May 2020 (estimated)
Last update
Apr 8, 2019

Study contacts

Norma Olvera
principal investigator · University of Houston

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Apr 2019. You cannot join it, but the record below documents what was studied.

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