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Playful Physical Activity for Executive Functions and School Readiness in Preschool Children (PPA-EF-SR)

30 juin 2026 mis à jour par: Assoc. Prof. Dr. Özgür EKEN, Inonu University

Effects of a Cognitively Enriched Playful Physical Activity Program on Executive Functions and School Readiness in Preschool Children

Executive functions, such as attention, inhibition, working memory, and planning, are important for early learning and school readiness in preschool children. This completed randomized controlled trial evaluated whether an 8-week cognitively enriched playful physical activity program could support executive functions and school readiness in preschool children compared with the regular physical education curriculum.

Preschool children were assigned to either a playful physical activity intervention group or a control group receiving conventional physical education. The intervention included structured movement-based games designed to combine physical activity with cognitive challenges, including response inhibition, working memory, planning, rule following, and cooperative problem solving. Outcomes included measures of executive functions and school readiness domains, including mathematical, linguistic, and social competence.

Aperçu de l'étude

Description détaillée

This study was designed as a completed, two-arm randomized controlled trial conducted in preschool children. The purpose of the study was to examine whether a cognitively enriched playful physical activity program could improve executive functions and school readiness compared with the regular physical education curriculum.

The experimental intervention consisted of an 8-week Playful Physical Activities program. The program included structured movement games designed to engage both motor and cognitive processes. Activities targeted gross and fine motor skills while incorporating executive-function demands such as selective attention, inhibitory control, working memory, planning, rule maintenance, and cooperative problem solving. Sessions included playful tasks related to language, mathematics, and social interaction, with the aim of supporting both cognitive development and school readiness in an age-appropriate educational setting.

Children in the control group continued to receive the conventional physical education curriculum over the same intervention period. The control condition involved regular age-appropriate physical education activities without the systematic integration of structured executive-function challenges or cognitive-motor dual-task components.

Participants were preschool children aged approximately 55 to 64 months. Eligible children were enrolled in participating preschool settings and were able to take part in physical activity sessions. Children with motor or mental disorders that could interfere with participation or outcome assessment were excluded.

The primary focus of the study was school readiness, including mathematical, linguistic, and social competence. Secondary outcomes included executive-function measures related to attention, inhibition, visuospatial memory, and planning/visuospatial organization. Assessments were conducted before and after the intervention period.

The study was conducted in accordance with ethical approval from the Local Research Ethics Committee at the High Institute of Sports and Physical Education of Ksar Said. The study has been completed.

Type d'étude

Interventionnel

Inscription (Réel)

48

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Tunis, Tunisie, 1003
        • Physical Activity, Sport and Health Research Unit UR18JS01, National Observatory of Sport

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Enfant

Accepte les volontaires sains

Oui

La description

Inclusion Criteria:

  • Preschool children aged 55 to 64 months.
  • Enrollment in one of the participating preschools.
  • Ability to participate in age-appropriate physical activity sessions.
  • Written informed consent provided by parents or legal guardians.

Exclusion Criteria:

  • Motor or intellectual disabilities that could prevent participation in physical activity sessions.
  • Diagnosed neurological, psychiatric, or developmental disorders, including attention-deficit/hyperactivity disorder or autism spectrum disorder.
  • Uncorrected visual or auditory impairments that could affect test performance.
  • Use of medication known to affect the central nervous system.
  • Absence from post-intervention testing or failure to complete the study procedures.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Playful Physical Activities Intervention
Preschool children assigned to this group received the 8-week Playful Physical Activities intervention.
The 8-week Playful Physical Activities intervention consisted of structured movement-based games integrating executive function challenges, including response inhibition, working memory, attention, planning, and cooperative problem-solving. Sessions were delivered three times per week for 60 minutes per session.
Autres noms:
  • APP
The control intervention consisted of the regular physical education curriculum delivered for 8 weeks, three times per week for 60 minutes per session. Sessions included traditional age-appropriate physical education activities without systematically embedded cognitive-motor executive function challenges.
Autres noms:
  • Conventional Physical Education
Comparateur actif: Regular Physical Education Curriculum
Preschool children assigned to this group received the regular physical education curriculum for 8 weeks.
The 8-week Playful Physical Activities intervention consisted of structured movement-based games integrating executive function challenges, including response inhibition, working memory, attention, planning, and cooperative problem-solving. Sessions were delivered three times per week for 60 minutes per session.
Autres noms:
  • APP
The control intervention consisted of the regular physical education curriculum delivered for 8 weeks, three times per week for 60 minutes per session. Sessions included traditional age-appropriate physical education activities without systematically embedded cognitive-motor executive function challenges.
Autres noms:
  • Conventional Physical Education

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in School Readiness Scores From Baseline to Post-intervention
Délai: Baseline and immediately after the 8-week intervention
School readiness was assessed using mathematical competence, linguistic competence, and social competence scores. Higher scores indicated better school readiness.
Baseline and immediately after the 8-week intervention

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change in Go/No-Go Task Error Rate From Baseline to Post-intervention
Délai: Baseline and immediately after the 8-week intervention
Inhibitory control was assessed using the Go/No-Go task. The outcome was the number of commission errors, with lower scores indicating better inhibitory control.
Baseline and immediately after the 8-week intervention
Change in Brief Visuospatial Memory Test-Revised Immediate Recall Score From Baseline to Post-intervention
Délai: Baseline and immediately after the 8-week intervention
Visuospatial memory was assessed using the BVMT-R immediate recall raw score. Higher scores indicated better visuospatial memory performance.
Baseline and immediately after the 8-week intervention
Change in Brief Visuospatial Memory Test-Revised Delayed Recall Score From Baseline to Post-intervention
Délai: Baseline and immediately after the 8-week intervention
Delayed visuospatial recall was assessed using the BVMT-R delayed recall raw score. Higher scores indicated better delayed recall performance.
Baseline and immediately after the 8-week intervention
Change in Rey-Osterrieth Complex Figure Test Copy Score From Baseline to Post-intervention
Délai: Baseline and immediately after the 8-week intervention
Visuospatial organization and planning were assessed using the Rey-Osterrieth Complex Figure Test copy score. Higher scores indicated better visuospatial planning and organization.
Baseline and immediately after the 8-week intervention

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

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Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

7 avril 2025

Achèvement primaire (Réel)

23 mai 2025

Achèvement de l'étude (Réel)

23 mai 2025

Dates d'inscription aux études

Première soumission

25 juin 2026

Première soumission répondant aux critères de contrôle qualité

25 juin 2026

Première publication (Réel)

1 juillet 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

2 juillet 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

30 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • PPA-EF-SR-2025
  • 41034 (Identificateur de registre: Pan African Clinical Trials Registry (PACTR); official trial number pending)

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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