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Effect of Sports Based Structured Cognitive Therapy Program on Attention, Memory and Behavior for School Going Children

25 augusti 2026 uppdaterad av: Riphah International University

Effect of a Sports-Based Structured Cognitive Therapy Program on Attention, Memory, and Behavior in School-Going Children: A Randomized Controlled Trial

This randomized controlled trial will evaluate the effect of a sports-based structured cognitive therapy program on attention, memory, and behavior in school-going children aged 8-12 years with mild to moderate attention or behavioral difficulties. A total of 52 participants will be randomly allocated to either an experimental group receiving an 8-week sports-based structured cognitive therapy program or a control group receiving conventional physical activity. The intervention will be delivered three times per week. Outcomes will be assessed at baseline, Week 4, and Week 8 using the Stroop Test, Teacher Report Form (TRF), and Behavior Rating Scale to determine changes in attention, memory, and behavior

Studieöversikt

Detaljerad beskrivning

This randomized controlled trial aims to evaluate the effectiveness of a sports-based structured cognitive therapy program on attention, memory, and behavior in school-going children aged 8-12 years with mild to moderate attention or behavioral difficulties. The primary objective is to determine whether participation in an 8-week sports-based structured cognitive therapy program improves attention, memory, and behavior compared with conventional physical activity. Attention will be assessed using the Stroop Test, behavioral and academic functioning using the Teacher Report Form (TRF), and behavior using the Behavior Rating Scale.

Studietyp

Interventionell

Inskrivning (Beräknad)

52

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studera Kontakt Backup

  • Namn: noreen khan, Phd
  • Telefonnummer: 03369687196

Studieorter

    • Kpk
      • Chak Six Hundred Twenty-four, Kpk, Pakistan, 25000
        • Rekrytering
        • Gghss Sarai Naimat Khan Haripur

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Barn

Tar emot friska volontärer

Ja

Beskrivning

Inclusion Criteria:

  • School-going children aged 8-12 years.
  • Children with mild to moderate attention or behavioral difficulties.
  • Children enrolled in participating primary or secondary schools in Haripur District.
  • Written informed consent obtained from a parent or legal guardian.

Exclusion Criteria:

  • Children diagnosed with severe neurological or psychiatric disorders.
  • Children with physical disabilities that prevent participation in sports-based activities.
  • Children currently participating in another structured cognitive or physical intervention program.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Stödjande vård
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Sports-Based Structured Cognitive Therapy
Participants assigned to the experimental group will receive an 8-week Sports-Based Structured Cognitive Therapy Program delivered three sessions per week, with each session lasting 45-60 minutes. The intervention integrates structured physical activities with cognitive tasks targeting attention, memory, executive function, and behavioral regulation. Activities include aerobic exercises, attention drills, memory exercises, and behavior-regulation games delivered at moderate to vigorous intensity.
Participants will receive an 8-week Sports-Based Structured Cognitive Therapy Program delivered three times per week. The program combines structured physical activities with cognitive tasks designed to improve attention, memory, executive function, and behavioral regulation through attention drills, memory exercises, and behavior-regulation games.
Aktiv komparator: Conventional Physical Activity
Participants assigned to the control group will receive conventional physical activity consisting of routine exercise-based activities supervised by a licensed physical therapist. Sessions will be conducted three times per week for 45-60 minutes over 8 weeks and will include warm-up exercises, stretching, balance activities, classroom games, and cool-down exercises without structured cognitive-sports integration.
Participants will receive conventional physical activity consisting of routine exercise-based activities including warm-up exercises, stretching, balance activities, classroom games, and cool-down exercises for 45-60 minutes per session, three sessions per week for 8 weeks, without structured cognitive training.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Stroop Interference Score
Tidsram: Baseline, Week 4, and Week 8
The Stroop Test will be used to assess selective attention and inhibitory control. The outcome will be measured using the Stroop Interference Score. Lower interference scores indicate better inhibitory control and attention.
Baseline, Week 4, and Week 8
Teacher Report Form (TRF) T-score
Tidsram: Baseline, Week 4, and Week 8
The Teacher Report Form (TRF) will be used to assess behavioral, emotional, and academic functioning in the school environment. The outcome will be summarized using the standardized TRF T-score according to the scoring procedures of the instrument.
Baseline, Week 4, and Week 8
Behavior Rating Scale Total Score
Tidsram: Baseline, Week 4, and Week 8
The Behavior Rating Scale will be used to assess behavioral functioning in children. The outcome will be summarized using the total score obtained according to the scoring procedures of the scale.
Baseline, Week 4, and Week 8

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Movement-Sequence Recall Score
Tidsram: Baseline, Week 4, and Week 8
Memory performance will be assessed using a movement-sequence recall task. The outcome will be summarized as the number of movement sequences correctly recalled.
Baseline, Week 4, and Week 8
Number Recall Score
Tidsram: Baseline, Week 4, and Week 8
Memory performance will be assessed using a number-recall task. The outcome will be summarized as the number of numerical sequences correctly recalled.
Baseline, Week 4, and Week 8
Word Recall Score
Tidsram: Baseline, Week 4, and Week 8
Memory performance will be assessed using a word-recall task. The outcome will be summarized as the number of words correctly recalled.
Baseline, Week 4, and Week 8

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

  • Huvudutredare: Zobia Naseem, MS, Riphah International University

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

16 augusti 2026

Primärt slutförande (Beräknad)

1 oktober 2026

Avslutad studie (Beräknad)

30 oktober 2026

Studieregistreringsdatum

Först inskickad

5 augusti 2026

Först inskickad som uppfyllde QC-kriterierna

25 augusti 2026

Första postat (Faktisk)

26 augusti 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

26 augusti 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

25 augusti 2026

Senast verifierad

1 augusti 2026

Mer information

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Ytterligare relevanta MeSH-villkor

Andra studie-ID-nummer

  • Aqsa Imtiaz

Plan för individuella deltagardata (IPD)

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NEJ

Läkemedels- och apparatinformation, studiedokument

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