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CompletedNCT07771959PBMT-DCUpdated Oct 5, 2026

Play-Based Motor Training in Children Aged 7-10 Years

An interventional study of Structured Play-Based Motor Training Program and Usual Physical Education in Healthy Volunteers and Child Development, sponsored by Islamic Azad University, Sanandaj. Completed at 1 site in China. Open to participants aged 7 Years to 10 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-05.

Sponsored by Islamic Azad University, Sanandaj · Not applicable, Interventional, and Other

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Feb 2026, registered Aug 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
7 Years to 10 Years
Sex
All
01

Study summary

This randomized controlled study evaluated the effects of an 8-week structured play-based motor training program on motor competence in children (boys and girls) aged 7-10 years. Eighty eligible participants (40 boys and 40 girls) were individually randomized in a 1:1 ratio to an intervention group or a usual physical-education control group. The intervention consisted of 24 play-based motor-training sessions delivered three times per week for 60 minutes, whereas the control group continued usual physical education twice per week for 40 minutes. The primary outcome was motor competence assessed using the MABC-2 total score. Cognitive test performance measured using the Kay Cognitive-Diagnostic Test and parent-rated executive-function difficulties measured using the BRIEF Parent Form were exploratory secondary outcomes. Posttest outcomes were compared between groups using ANCOVA with the corresponding baseline score as a covariate. This study record was created retrospectively after completion of the study.

Read the detailed description

The study was conducted during the 2025-2026 academic year in Dongchuan District, Yunnan Province, China. The sampling frame comprised approximately 100 children (50 boys and 50 girls) from four eligible classes across two primary schools. One hundred children were randomly selected by lottery for eligibility assessment. Twenty children were excluded before allocation: twelve because of physical or motor conditions that did not meet eligibility requirements, six because parental consent was not provided, and two because child assent was not obtained.

The remaining 80 eligible participants (40 boys and 40 girls) were individually randomized in a 1:1 ratio to the intervention or control group using a computer-generated random allocation sequence. Allocation was concealed using sequentially numbered, opaque, sealed envelopes prepared independently and opened after completion of baseline assessments.

The intervention group received an 8-week structured play-based motor-training program comprising 24 sessions, with three 60-minute sessions per week. Sessions included social interaction, warm-up, play-based motor activities, cool-down, and feedback. Main activities included coordinated movement with children's rhymes, animal-imitation games, running, jumping, throwing, rolling, and ball activities. The control group continued usual physical education twice weekly for approximately 40 minutes per session.

MABC-2 and Kay assessments were conducted by an independent trained assessor blinded to group allocation. Parents completing the BRIEF were not blinded. The primary outcome was the MABC-2 total score. Kay total score and BRIEF mean item score were treated as exploratory secondary outcomes. All 80 randomized participants completed posttest assessment. No serious or intervention-related adverse events were reported.

02

Conditions studied

  • Healthy Volunteers
  • Child Development

Keywords

  • play-based motor training
  • motor competence
  • MABC-2
  • children
  • executive function
  • cognitive performanc
  • physical education
  • motor skills
03

In context

Lead sponsor

Islamic Azad University, Sanandaj is the lead sponsor of 29 studies on the registry; 2 are open to participants now.

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

04

Who can participate

Ages eligible
7 Years to 10 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Children aged 7-10 years
  • Enrolled in one of the eligible primary-school classes included in the study sampling frame
  • Able to participate in regular school physical-education and play-based motor activities
  • Written provided by a parent or legal guardian Child assent provided

Exclusion criteria

Exclusion Criteria:

  • A physical or motor condition that prevented safe or effective participation in the intervention or assessments
  • Parental or guardian consent not provided
  • Child assent not provided
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
80 participants (actual)

Study arms

  • Experimental
    Structured Play-Based Motor Training

    Participants received an 8-week structured play-based motor-training program consisting of three 60-minute sessions per week (24 sessions; 1,440 planned minutes). Each session included 5 minutes of social/introductory activity, 5 minutes of warm-up, 40 minutes of play-based motor activities, 5 minutes of cool-down, and 5 minutes of feedback.

    Behavioral: Structured Play-Based Motor Training Program

  • Active comparator
    Usual Physical Education

    Participants continued their usual school physical-education program consisting of two approximately 40-minute sessions per week, including general fitness activities, running, stretching, and simple recreational games, without the structured play-based motor-training protocol.

    Behavioral: Usual Physical Education

Interventions

  • BehavioralStructured Play-Based Motor Training Program

    Participants in the intervention arm received an 8-week structured play-based motor training program delivered three times per week for 60 minutes per session, for a total of 24 sessions. Each session followed a standardized 60-minute format consisting of 5 minutes of social/introductory interaction, 5 minutes of warm-up activities, 40 minutes of structured play-based motor activities, 5 minutes of cool-down, and 5 minutes of feedback. The main activity component included coordinated movements accompanied by children's rhymes, animal-imitation games, and fundamental motor activities such as running, jumping, throwing, rolling, and simple ball-handling tasks. Activities were delivered in a game-based format and emphasized active participation, movement exploration, coordination, and repeated practice of fundamental movement skills. The intervention replaced the participants' usual physical-education sessions during the study period.

  • BehavioralUsual Physical Education

    Participants in the control arm continued their usual school physical-education program throughout the 8-week study period. Usual physical education was delivered twice per week for approximately 40 minutes per session and included general fitness activities, running, stretching, and simple recreational games. The control program did not include the structured play-based motor training protocol, the standardized 5+5+40+5+5 session format, or the systematic motor-practice activities used in the intervention arm. Control sessions were scheduled separately from the intervention sessions, and control participants did not observe the structured intervention activities.

06

What researchers measure

Primary outcomes

  1. MABC-2 Total Score

    Motor competence was assessed using the Movement Assessment Battery for Children, Second Edition (MABC-2), using the age-appropriate Age Band 2 procedures. The MABC-2 total score was used as the primary motor-performance outcome. Higher scores indicate better motor performance. The primary statistical comparison used posttest scores adjusted for the corresponding baseline score using ANCOVA.

    Time frame: Baseline and approximately 9 weeks after baseline (one week after completion of the 8-week intervention)

Secondary outcomes

  1. Kay Cognitive-Diagnostic Test Total Score

    Cognitive test performance was assessed using the Kay Cognitive-Diagnostic Test. Five subtests assessed concept formation, symbolic thinking, socialization of thought, visual-motor perception, and short-term attention/psychomotor speed. The total score ranges theoretically from 0 to 100, with higher scores indicating better performance. A translated Chinese version was used without formal age-specific validation; therefore, this outcome was considered exploratory.

    Time frame: Baseline and approximately 9 weeks after baseline

  2. BRIEF Parent-Form Mean Item Score

    Executive-function difficulties were assessed using the 86-item Chinese parent form of the Behavior Rating Inventory of Executive Function (BRIEF). Items were rated from 1 (never) to 3 (often), and the mean item score was calculated across the 86 items. Higher scores indicate greater parent-rated executive-function difficulties. The same parent or caregiver completed the questionnaire at baseline and posttest. This was an exploratory secondary outcome.

    Time frame: Baseline and approximately 9 weeks after baseline

07

Study locations

1 site
  • Dongchuan, Yunnan, China
    Dongchuan, Yunnan 654100, China
08

References and documents

Individual participant data

Plan to share: Undecided — Individual participant data are not publicly available because of ethical and confidentiality restrictions. Requests for access to de-identified data may be considered on a case-by-case basis by the corresponding author, subject to approval by the relevant institutional and ethics authorities and applicable confidentiality requirements.

No publications or documents are linked to this record.

09

Updates

2 registry updates since Sep 25, 2026
Minor edits
Nothing that changes what the study is or who can join. Edited: verification date
2 updates, last Oct 5, 2026
Show all 2 updates
  1. Oct 5, 2026
    Minor edits only
    + 1 other change: verification date
  2. Oct 2, 2026
    Minor edits only
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07771959
Lead sponsor
Islamic Azad University, Sanandaj
Collaborators
Islamic Azad University of Mashhad
Responsible party
Zinat Ebrahimi (Assistant Professor, Islamic Azad University, Sanandaj) — Principal investigator
First posted
Aug 19, 2026
Start date
Feb 15, 2026
Primary completion
Apr 20, 2026
Completion
Jul 7, 2026
Last update
Oct 5, 2026

Oversight

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

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This study is completed, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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