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

30 de junho de 2026 atualizado por: 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.

Visão geral do estudo

Descrição detalhada

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.

Tipo de estudo

Intervencional

Inscrição (Real)

48

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

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

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Filho

Aceita Voluntários Saudáveis

Sim

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Prevenção
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: 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.
Outros nomes:
  • PPA
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.
Outros nomes:
  • Conventional Physical Education
Comparador Ativo: 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.
Outros nomes:
  • PPA
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.
Outros nomes:
  • Conventional Physical Education

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Change in School Readiness Scores From Baseline to Post-intervention
Prazo: 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

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Change in Go/No-Go Task Error Rate From Baseline to Post-intervention
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

7 de abril de 2025

Conclusão Primária (Real)

23 de maio de 2025

Conclusão do estudo (Real)

23 de maio de 2025

Datas de inscrição no estudo

Enviado pela primeira vez

25 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

25 de junho de 2026

Primeira postagem (Real)

1 de julho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

2 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

30 de junho de 2026

Última verificação

1 de junho de 2026

Mais Informações

Termos relacionados a este estudo

Outros números de identificação do estudo

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

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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