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Play-Based Motor Training in Children Aged 7-10 Years (PBMT-DC)

2 de octubre de 2026 actualizado por: Zinat Ebrahimi, Islamic Azad University, Sanandaj

Effects of an 8-Week Play-Based Motor Training Program on Motor Competence, Cognitive Test Performance, and Parent-Rated Executive Function in Children Aged 7-10 Years: A Randomized Controlled Trial

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.

Descripción general del estudio

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Actual)

80

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Yunnan
      • Dongchuan, Yunnan, Porcelana, 654100
        • Dongchuan, Yunnan, China

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

7 años a 10 años (Niño)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

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 informed consent provided by a parent or legal guardian Child assent provided

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Otro
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
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.

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.

Comparador activo: 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.

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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
MABC-2 Total Score
Periodo de tiempo: Baseline and approximately 9 weeks after baseline (one week after completion of the 8-week intervention)

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.

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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Kay Cognitive-Diagnostic Test Total Score
Periodo de tiempo: Baseline and approximately 9 weeks after baseline

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.

Baseline and approximately 9 weeks after baseline
BRIEF Parent-Form Mean Item Score
Periodo de tiempo: Baseline and approximately 9 weeks after baseline

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.

Baseline and approximately 9 weeks after baseline

Colaboradores e Investigadores

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Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

15 de febrero de 2026

Finalización primaria (Actual)

20 de abril de 2026

Finalización del estudio (Actual)

7 de julio de 2026

Fechas de registro del estudio

Enviado por primera vez

9 de agosto de 2026

Primero enviado que cumplió con los criterios de control de calidad

17 de agosto de 2026

Publicado por primera vez (Actual)

19 de agosto de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

5 de octubre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

2 de octubre de 2026

Última verificación

1 de agosto de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • PBMT-DONGCHUAN-2025

Plan de datos de participantes individuales (IPD)

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INDECISO

Descripción del plan IPD

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.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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