Assessing Impact of Active Learning on Student Outcomes: Texas Initiatives for Children's Activity and Nutrition (ICAN) (ICAN)

June 22, 2017 updated by: University of Texas at Austin

A Cluster Randomized Control Trial to Assess the Impact of Active Learning on Child Activity, Attention Control, and Academic Outcomes: The Texas I-CAN Trial

Background: Active learning is designed to pair physical activity with the teaching of academic content. This has been shown to be a successful strategy to increase physical activity and improve academic performance. The existing designs have confounded academic lessons with physical activity. As a result, it is impossible to determine if the subsequent improvement in academic performance is due to: (1) physical activity, (2) the academic content of the active learning, or (3) the combination of academic material taught through physical activity.

Methods / Design: The Texas I-CAN project is a 3-arm, cluster randomized control trial in which 28 elementary schools were assigned to either control, math intervention, or spelling intervention. As a result, each intervention condition serves as an unrelated content control for the other arm of the trial, allowing the impact of physical activity to be separated from the content. That is, schools that perform only active math lessons provide a content control for the spelling schools on spelling outcomes. This also calculated direct observations of attention and behavior control following periods of active learning.

Discussion: This design is unique in its ability to separate the impact of physical activity, in general, from the combination of physical activity and specific academic content. This, in combination with the ability to examine both proximal and distal outcomes along with measures of time on task will do much to guide the design of future, school-based interventions.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

2716

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • students in 4th grade in a participating elementary school and their 4th grade teachers

Exclusion Criteria:

  • none

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Texas I-CAN Active Math Lessons
Texas I-CAN Active math lesson in academic classroom
physically active, academic lessons in the elementary school classroom
Experimental: Texas I-CAN Active Language Arts Lessons
Texas I-CAN Active language arts lessons in academic classroom
physically active, academic lessons in the elementary school classroom
No Intervention: Control
Regular, Sedentary academic lessons in math and language arts

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Physical activity level
Time Frame: one school week
time in moderate to vigorous physical activity
one school week
Time on task
Time Frame: change in time on task from baseline to 15 minutes post academic lesson
student attentional focus in the classroom 15 minutes prior to and 15 minutes post active lesson implemented in the classroom on one school day
change in time on task from baseline to 15 minutes post academic lesson
Acute academic achievement
Time Frame: change in math and language arts scores from Baseline to 2 weeks
acute academic scores on math and language arts test developed by fourth grade teacher
change in math and language arts scores from Baseline to 2 weeks
Long-term math achievement
Time Frame: Change in math achievement scores from Baseline to 7 months
Academic scores on math sub tests (Calculation, Fluency) of the Woodcock Johnson III
Change in math achievement scores from Baseline to 7 months
Long-term language arts achievement
Time Frame: Change in language arts achievement from Baseline to 7 months
Academic scores on spelling sub test of the Woodcock Johnson III and comprehension section of Gates MacGinitie test
Change in language arts achievement from Baseline to 7 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: John B Bartholomew, PHD, UT Austin

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 15, 2012

Primary Completion (Actual)

May 31, 2015

Study Completion (Actual)

May 31, 2015

Study Registration Dates

First Submitted

March 9, 2017

First Submitted That Met QC Criteria

March 15, 2017

First Posted (Actual)

March 22, 2017

Study Record Updates

Last Update Posted (Actual)

June 26, 2017

Last Update Submitted That Met QC Criteria

June 22, 2017

Last Verified

June 1, 2017

More Information

Terms related to this study

Other Study ID Numbers

  • 1R01HD070741 (U.S. NIH Grant/Contract)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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