The CHAMP ASP: Promoting Physical Activity & Health in Children (CHAMP-ASP)

February 25, 2026 updated by: Leah Robinson, University of Michigan

The CHAMP Afterschool Program: Promoting Physical Activity & Health in Children

Currently, 10 million children participate in afterschool programs (ASPs) each day, and ASPs provide a great opportunity to enhance children's health outside of the regular school environment, particularly given the decline in physical education. This proposed, randomized cluster, controlled trial will examine the immediate (pre- to post-test) and sustained (1-year post-intervention follow-up) effects of CHAMP-ASP on physical activity (primary outcome), motor performance, perceived motor competence, health-related physical fitness, and weight status. CHAMP-ASP will be implemented by ASP staff and will be conducted in ASPs located in Ypsilanti/Ann Arbor, Michigan. Children (N = 264; CHAMP-ASP=132 and control=132) K-2 graders (typically ages 5-8 years) will participate 35 minutes/day X 3-4 days/week for 19 weeks (dose of 1995 - 2240 minutes). The aims are to: a) examine the immediate and sustained effects of CHAMP-ASP on physical activity, motor performance, and perceived motor competence relative to the control ASP, b) examine the immediate and sustained effects of CHAMP-ASP on secondary health outcomes - health-related physical fitness (cardiorespiratory fitness, muscular strength), and weight status compared to children in schools randomized to control ASP, and c) determine if perceived motor competence mediates the effect of CHAMP-ASP on moderate-to-vigorous physical activity.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

Promoting health-enhancing and sustainable physical activity levels across childhood and adolescence contributes to adult health. The Children's Health Activity Motor Program (CHAMP) is an evidence-based intervention that demonstrates impactful results on motor performance, perceived motor competence, and physical activity in physical education and movement-based settings. Currently, 10 million children participate in afterschool programs (ASPs) each day, and ASPs provide a great opportunity to enhance children's health outside of the regular school environment, particularly given the decline in physical education. This proposed, randomized cluster, controlled trial will examine the immediate (pre- to post-test) and sustained (1-year post-intervention follow-up) effects of CHAMP-ASP on physical activity (primary outcome), motor performance, perceived motor competence, health-related physical fitness, and weight status. CHAMP-ASP will be implemented by ASP staff and will be conducted in ASPs located in Ypsilanti/Ann Arbor, Michigan. Children (N = 264; CHAMP-ASP=132 and control=132) K-2 graders (typically ages 5-8 years) will participate 35 minutes/day X 3-4 days/week for 19 weeks (dose of 1995 - 2240 minutes). The aims are to: a) examine the immediate and sustained effects of CHAMP-ASP on physical activity, motor performance, and perceived motor competence relative to the control ASP, b) examine the immediate and sustained effects of CHAMP-ASP on secondary health outcomes - health-related physical fitness (cardiorespiratory fitness, muscular strength), and weight status compared to children in schools randomized to control ASP, and c) determine if perceived motor competence mediates the effect of CHAMP-ASP on moderate-to-vigorous physical activity. The long-term goal is to provide a sustainable, ecologically-relevant, and evidence-based program during the early elementary years that is health-enhancing and increases physical activity in school-age children. Findings could significantly influence future physical activity interventions and support a sustainable, ecologically-relevant (delivered by ASP staff) evidence-based program (i.e., CHAMP) that contributes to long-term health-enhancing physical activity and health in children.

Study Type

Interventional

Enrollment (Actual)

264

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Michigan
      • Ann Arbor, Michigan, United States, 48104
        • Leah Elizabeth Robinson

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

1 year to 4 years (Child)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

-Participants must be attending an ASP in the Ann-Arbor/Ypsilanti and Lansing/East Lansing area

Exclusion Criteria:

  • Participants diagnosed with syndromes or diseases that affect PA participation
  • Participants diagnosed with any major illness, developmental, and/or physical disability that limited their ability to participate in movement and physical activity programs.

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: CHAMP-ASP

CHAMP, is a mastery climate motor skills intervention, that provides children the opportunity to establish behaviors that reinforce decision-making while participating in a motor activity tasks. Children will participate in CHAMP for 35 minutes/day 3-4 days per week for 19 weeks.

Each 35-min session consists of three parts:

  1. 3-5 min of motor skill introductory activity that includes a group motor activity, the teaching of the lesson that includes a demonstration and understanding of developmentally appropriate learning clues;
  2. 25 min of motor skill instruction and practice (i.e., 'active motor engagement'), participants will be encouraged to move through 3-4 motor activity stations that align with the TARGET structure; and
  3. 3 -5 min motor skill closure activity that involves a review of the lesson and critical elements.
The behavioral motor skill intervention (CHAMP) is an intervention strategy that uniquely address differences in children's development. CHAMP does not equate to a "one size fits all" approach. Children will be in an environment that promotes opportunities for them to development improvement in motor skills based on their specific individual needs and choices. The CHAMP intervention promotes a mastery climate that allows each individual child to be successful and learn while promoting intrinsic motivation and autonomy. CHAMP consists of 35 minutes/day X 3-4 days/week for 19 weeks (dose of 1995 - 2240 minutes). Each session will consist of three parts: (a) 3-5 min of motor skill introductory activity, (b) 25 min of motor skill instruction and practice, and (c) 3-5 min motor skill closure activity.
No Intervention: Control - Standard of Practice
The Control (standard of practice) condition will be the school typical ASP and will be implemented according to the existing procedures.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Motor Competence - process measures
Time Frame: baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Process scores will be assessed with the Test of Gross Motor Development (TGMD, 3rd edition); scores from the two subscales (locomotor and ball skills) will be reported as raw scores for each skills and an overall score (total MC score). The project will assess changes overtime for this measure
baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Changes in Motor Competence - product measures
Time Frame: baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Product scores will use throwing speed, kicking speed, jump distance, running speed, and hopping speed. Product score will vary for each participant (i.e., kick, run, hopping, and throw velocity along with jumping distance - faster scores and greater distance are indicators of better MC).
baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Changes in Physical Activity
Time Frame: baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Actigraph GTX3+ tri-axial accelerometer will be used to measure the frequency, intensity, and duration of PA among children during the ASP and in free-living settings. Participants will be asked to wear the same accelerometer for 7 full days (5 week and 2 weekend days). Data will be set to collect data in raw mode (30 Hz), and will be processed using ActiLife software or other, more advanced techniques, such as machine learning approaches.
baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Changes in Health-related fitness - Cardiorespiratory endurance
Time Frame: baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Cardiorespiratory endurance will be assessed with a 6-min walk test. For the 6-min walk test, the children walk as fast as possible around two cones for 6 minutes.
baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Changes in Health-related fitness - Muscular Strength
Time Frame: baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Muscular strength will be assessed with test of handgrip strength. Upper body strength will be assessed using a hand grip strength with a dynamometer, which has been deemed reliable and valid in 6-12-year-olds [62]. Grip will be appropriately adjusted for size, and two trials on the right and left sides (elbow extended) will be assessed (muscular strength). The sum of maximum score (kg) of two trials for each hand will be used in analyses.
baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Changes in Health-related fitness - Body Composition
Time Frame: baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Body composition (i.e., body fat) will be assessed with bioelectrical impedance. Body fat percentage will be the average of two measurements assessed (to the nearest 0.1%, respectively) with a bioelectric impedance analysis scale (Tanita). The assessment will be completed in a designated, private area
baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Demographics
Time Frame: Baseline
Date of birth, sex, race/ethnicity, and grade will be collected through self-report through the IRB consenting process by the parent/guardian.
Baseline
Changes in Perceived Motor Competence (Global)
Time Frame: baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Will be assessed with the Harter and Pike Pictorial Scale of PMC and Social Acceptance (PSPCSA). The PSPCSA will be used to measure the child's global perceived physical competence. The PSPCSA physical competence subscale consists of six items that are presented in pictures and each child will select a picture that is more like them. The six items included are swinging, climbing, tying shoe laces, skipping, running, and hopping. For the assessment, children will (1) select the picture that is most like him or herself. One picture depicts a child who is competent and the other shows a child who is not skilled; (2) focus on the designated pictures and indicate whether he or she is just a "little bit" or "a lot" like that child. Separate pictures for girls and boys will be used in accordance with the manual procedures. The range of scores for each item on the subscale is 1 (low competence) to 4 (high competence).
baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Changes in Digital Scale of Perceived Motor Competence (DSPMC)
Time Frame: baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Will be assessed with the Digital Scale of Perceived Motor Competence (DSPMC) The DSPMC is a video-based assessment that allows the child to see the entire motor skill in action (video) rather than a static picture. The scale is the identical layout and item structure to the PSPCSA but align with the 12 fundamental motor skills of the TGMD For the assessment, children will (1) select the video that is most like him or herself. One video depicts a child who is competent and the other shows a child who is not skilled; (2) focus on the designated videos and indicate whether he or she is just a "little bit" or "a lot" like that child. The range of scores for each item on the subscale is 1 (low competence) to 4 (high competence).
baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
CHAMP ASP Acceptability Questionnaire
Time Frame: post-intervention (i.e., 24 weeks post baseline)
Children will complete an acceptability survey to provide information on how they like participating in the CHAMP-ASP program. The CHAMP-ASP Acceptability Questionnaire consists of 6 questions about the program's features such as children's autonomy to determine for how long they want to be doing the selected activity and how the ASP staff provided them feedback. For each question the child will answer with yes or no.
post-intervention (i.e., 24 weeks post baseline)
Family Questionnaire
Time Frame: baseline
Parents will be asked to complete a family questionnaire to provide some descriptive information about their child and family. Questions are regarding the family structure, socio-economic status, physical activity habits, sleeping habits, and screen time habits. The questionnaire has closed ended questions that will be quantified for data analyses.
baseline
Changes Social-emotional measure
Time Frame: baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Parents will be asked to complete the Strength and Difficulties Questionnaire (SDQ) which is a relatively short instrument developed to screen for emotional and behavioural problems in children aged 3-16 years [59]. The SDQ is a 25-item questionnaire with three response categories from zero to two (not true, somewhat true, and certainly true). The questionnaire has five subscales of five items each: emotional problems, conduct problems, hyperactivity/inattention problems, peer problems, and prosocial behaviour.
baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Changes in Body Mass Index
Time Frame: baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up
Will be used to calculate body mass index (BMI) with height and weight will be assessed with the participant barefoot and in light clothing. Standing height will be measured to the nearest 0.1 cm using a portable stadiometer and the average of two measurements to the nearest 0.1 cm (Shorr Productions, Olney, MD). Weight will be the average of two measurements assessed (to the nearest 0.1 kg and 0.1%, respectively) with a weight scale. BMI will be calculated, and, using age and sex and the CDC growth charts,95 transformed into BMI z-score for analyses. The assessment will be completed in a designated, private area
baseline, post-intervention (i.e., 24 weeks post baseline), and 1 year post-intervention follow-up

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Leah E Robinson, PhD, University of Michigan

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.

General Publications

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)

December 1, 2022

Primary Completion (Estimated)

August 31, 2026

Study Completion (Estimated)

August 31, 2026

Study Registration Dates

First Submitted

March 16, 2022

First Submitted That Met QC Criteria

April 18, 2022

First Posted (Actual)

April 25, 2022

Study Record Updates

Last Update Posted (Actual)

February 27, 2026

Last Update Submitted That Met QC Criteria

February 25, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • HUM00208311
  • R01NR018830 (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

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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