CClinicalTrials.gg
Active, not recruitingNCT07485270Updated Mar 20, 2026

Development of Human Motor Skills and the Promotion of Motivation for Physical Activity

An interventional study of E-MOVE - Emotional Movement Program for Physical Education in Physical Inactivity, Obesity & Overweight and Motor Development, sponsored by Charles University, Czech Republic. Active, not recruiting at 9 sites in Czechia. Open to participants aged 8 Years to 11 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-03-20.

Sponsored by Charles University, Czech Republic · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 6 months after the study started (first participant enrolled Sep 2025, registered Mar 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
325
Allocation
Randomized
Ages
8 Years to 11 Years
Sex
All
01

Study summary

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.

02

Conditions studied

  • Physical Inactivity
  • Obesity & Overweight
  • Motor Development
  • Cognitive Development
  • Physical Activity
  • Physical Literacy
03

In context

Sedentary Behavior

332 studies on the registry are indexed under Sedentary Behavior; 155 are open to participants now.

This study's enrollment of 325 is above the median of 70 across 287 interventional studies indexed under Sedentary Behavior.

Browse Sedentary Behavior studies →

Lead sponsor

Charles University, Czech Republic is the lead sponsor of 220 studies on the registry; 76 are open to participants now.

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

04

Who can participate

Ages eligible
8 Years to 11 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Outcomes assessor)
Enrollment
325 participants (actual)

Study arms

  • No intervention
    Control group
  • Experimental
    Interventional 2

    intervention 5x a week

    Behavioral: E-MOVE - Emotional Movement Program for Physical Education

  • Experimental
    Interventional 1

    intervention 2x a week

    Behavioral: E-MOVE - Emotional Movement Program for Physical Education

Interventions

  • BehavioralE-MOVE - Emotional Movement Program for Physical Education

    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.

06

What researchers measure

Primary outcomes

  1. Cardiorespiratory fitness

    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.

    Time frame: Baseline and annually during the 3-year intervention

  2. Actual Motor Competence

    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.

    Time frame: Baseline and annually during the 3-year intervention

  3. Cognitive functions

    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.

    Time frame: Baseline and annually during the 3-year intervention

  4. Physical literacy

    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.

    Time frame: Baseline and annually during the 3-year intervention

  5. Motivation for physical activity

    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.

    Time frame: Baseline and annually during the 3-year intervention

  6. Body composition

    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.

    Time frame: Baseline and annually during the 3-year intervention

  7. Physical activity

    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.

    Time frame: Baseline and annually during the 3-year intervention

  8. Perceived Motor Competence

    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.

    Time frame: Baseline and annually during the 3-year intervention

07

Study locations

9 sites
  • ZŠ Laštůvkova
    Brno, Czechia 635 00, Czechia
  • ZŠ Heyrovského
    Brno, Czechia, Czechia
  • ZŠ Lomnice
    Lomnice, Czechia 356 01, Czechia
  • ZŠ Mlýnská
    Mohelnice, Czechia 789 85, Czechia
  • ZŠ Plzeň - Růžovka
    Pilsen, Czechia 301 00, Czechia
  • ZŠ Žernosecká
    Prague, Czechia 182 00, Czechia
  • ZŠ Lyčkovo náměstí
    Prague, Czechia 18600, Czechia
  • ZŠ Rudná
    Rudná, Czechia, Czechia
  • ZŠ Velké Popovice
    Velké Popovice, Czechia 251 69, Czechia
08

References and documents

Individual participant data

Plan to share: Yes

Supporting information: Study protocol, Sap, Icf, Csr, Analytic code

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 Mar 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07485270
Lead sponsor
Charles University, Czech Republic
Responsible party
Sponsor
First posted
Mar 20, 2026
Start date
Sep 11, 2025
Primary completion
Jun 2028 (estimated)
Completion
Jun 2029 (estimated)
Last update
Mar 20, 2026

Oversight

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

Not currently enrolling

This study is active, not recruiting, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion