- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07485270
Development of Human Motor Skills and the Promotion of Motivation for Physical Activity
March 16, 2026 updated by: Charles University, Czech Republic
University Centre of Excellence for Studies of Human Motoric at Faculty of Physical Education and Sport
This study is conducted within the University Centre of Excellence for Studies of Human Motoric at the Faculty of Physical Education and Sport, Charles University.
The project focuses on research investigating mechanisms that support motivation for participation in physical activity among children and youth.
In recent decades, participation in physical activity has been declining globally, including among children and adolescents.
Understanding the factors that influence motivation for physical activity is essential for developing effective strategies to support long-term engagement in physical activity.
The study aims to contribute to knowledge about the role of physical activity and physical education in promoting children's long-term physical and mental development.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
325
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
-
-
Czechia
-
Brno, Czechia, Czechia, 635 00
- ZŠ Laštůvkova
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Brno, Czechia, Czechia
- ZŠ Heyrovského
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Lomnice, Czechia, Czechia, 356 01
- ZŠ Lomnice
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Mohelnice, Czechia, Czechia, 789 85
- ZŠ Mlýnská
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Pilsen, Czechia, Czechia, 301 00
- ZŠ Plzeň - Růžovka
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Prague, Czechia, Czechia, 182 00
- ZŠ Žernosecká
-
Prague, Czechia, Czechia, 18600
- ZŠ Lyčkovo náměstí
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Rudná, Czechia, Czechia
- ZŠ Rudná
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Velké Popovice, Czechia, Czechia, 251 69
- ZŠ Velké Popovice
-
-
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
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Children enrolled in the 3rd grade of participating primary schools
- Written informed consent from a parent or legal guardian
- Willingness to participate in study assessments and the school-based intervention
Exclusion Criteria:
- Acute illness or injury at the time of enrollment or assessment
- Recovery from illness or injury limiting participation in physical activity
- Chronic medical condition limiting participation in physical activity
- Atypical neurodevelopment or diagnosed neurodevelopmental disorder that may affect participation in the intervention or assessments
- Any other condition judged by the investigators to prevent safe participation in study procedures
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: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control group
|
|
|
Experimental: Interventional 2
intervention 5x a week
|
A school-based physical education intervention delivered through tandem teaching by a physical education teacher and a trained coach five times per week.
The program is based on principles of Affective-Reflective Theory (ART) and aims to promote positive affective experiences during physical activity, supporting children's motivation, engagement, and long-term participation in physical activity.
|
|
Experimental: Interventional 1
intervention 2x a week
|
A school-based physical education intervention delivered through tandem teaching by a physical education teacher and a trained coach five times per week.
The program is based on principles of Affective-Reflective Theory (ART) and aims to promote positive affective experiences during physical activity, supporting children's motivation, engagement, and long-term participation in physical activity.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Cardiorespiratory fitness
Time Frame: Baseline and annually during the 3-year intervention
|
Cardiorespiratory fitness assessed using the 20-m shuttle run test (Leger test).
The outcome was expressed as the number of completed shuttle runs.
Higher numbers of completed shuttle runs indicate better cardiorespiratory fitness.
|
Baseline and annually during the 3-year intervention
|
|
Actual Motor Competence
Time Frame: Baseline and annually during the 3-year intervention
|
Motor competence assessed using the Canadian Agility and Movement Skill Assessment (CAMSA).
The Canadian Agility and Movement Skill Assessment (CAMSA) raw score consists of the sum of the skill score and the time score.
The skill score and time score each have a maximum of 14 points, yielding a total raw score of 1 to 28.
Higher scores indicate better motor competence.
|
Baseline and annually during the 3-year intervention
|
|
Cognitive functions
Time Frame: Baseline and annually during the 3-year intervention
|
Selected cognitive functions is assessed using the Woodcock-Johnson cognitive test battery.
For the present study, results are recommended to be reported as standard scores, which are age-normed with a mean of 100 and a standard deviation of 15.
Higher scores indicate better cognitive performance relative to age-matched peers.
|
Baseline and annually during the 3-year intervention
|
|
Physical literacy
Time Frame: Baseline and annually during the 3-year intervention
|
Physical literacy assessed using the Physical Literacy in Children Questionnaire (PLC-Q).
The Physical Literacy in Children Questionnaire (PL-C Quest) consists of 30 items across four domains.
Each item is scored on a 1-4-point scale, yielding a total score of 30-120.
Higher scores indicate higher self-perceived physical literacy.
Thus, higher total scores reflect a higher level of physical literacy.
|
Baseline and annually during the 3-year intervention
|
|
Motivation for physical activity
Time Frame: Baseline and annually during the 3-year intervention
|
Motivation for participation in physical activity is assessed using the AFFEXX questionnaire.
The Affective Exercise Experiences Questionnaire (AFFEXX) consists of 22 items, each rated on a 1-5-point scale, yielding a total score ranging from 22 to 110.
Higher scores indicate higher motivation for physical activity.
|
Baseline and annually during the 3-year intervention
|
|
Body composition
Time Frame: Baseline and annually during the 3-year intervention
|
Body composition is assessed using bioelectrical impedance analysis (BODYSTAT Quadscan 4000).
The outcome variables included body fat percentage, intracellular water (ICW), and extracellular water (ECW).
Higher body fat values indicate greater adiposity.
ICW and ECW represent the relative distribution of body water between the intracellular and extracellular compartments, respectively.
Body fat was interpreted using age- and sex-specific percentile cut-offs (<2nd percentile = underfat, 2nd to <85th percentile = normal, 85th to <95th percentile = overfat, and ≥95th percentile = obese), whereas ICW and ECW were interpreted relative to age- and sex-specific reference values, as fixed clinical cut-offs are not established for healthy pediatric populations.
|
Baseline and annually during the 3-year intervention
|
|
Physical activity
Time Frame: Baseline and annually during the 3-year intervention
|
Physical activity monitored using ActiGraph GT3X accelerometers.
Physical activity was objectively assessed using an ActiGraph GT3X accelerometer worn for 7 consecutive days during the week.
Data were used to quantify time spent in sedentary behavior, light physical activity (LPA), moderate physical activity (MPA), and vigorous physical activity (VPA).
In addition, moderate-to-vigorous physical activity (MVPA) was calculated as the sum of moderate and vigorous physical activity.
This 7-day ActiGraph protocol is consistent with common practice in pediatric accelerometer studies.
The outcomes were expressed as time spent in each intensity category, typically reported in minutes per day.
Sedentary time reflects the amount of time spent inactive, whereas LPA, MPA, VPA, and MVPA reflect increasing levels of movement intensity.
Higher values of light, moderate, vigorous, or MVPA indicate that the child is more physically active.
|
Baseline and annually during the 3-year intervention
|
|
Perceived Motor Competence
Time Frame: Baseline and annually during the 3-year intervention
|
Perceived Motor Competence is assessed using the Pictorial Scale of Perceived Movement Skill Competence (PMSC).
The Pictorial Perceived Motor Competence (PMSC) instrument consists of 22 items, with each item rated on a 1-4-point scale.
The total score, therefore, ranges from 22 to 88 points.
Higher scores indicate higher perceived motor competence.
|
Baseline and annually during the 3-year intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this 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)
September 11, 2025
Primary Completion (Estimated)
June 1, 2028
Study Completion (Estimated)
June 1, 2029
Study Registration Dates
First Submitted
March 13, 2026
First Submitted That Met QC Criteria
March 16, 2026
First Posted (Actual)
March 20, 2026
Study Record Updates
Last Update Posted (Actual)
March 20, 2026
Last Update Submitted That Met QC Criteria
March 16, 2026
Last Verified
March 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 050824
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- ANALYTIC_CODE
- CSR
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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