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The Effect of Movement Education on Fundamental Biomotor Skills in Children Aged 6-9

2. september 2026 opdateret af: Sevinç SERİN YAMAN, Istanbul Gelisim University

The goal of this clinical trial is to learn if movement training improves speed, jumping ability, and flexibility in children aged 6 to 9.

The main questions it aims to answer are:

Does movement training improve sprint speed in young children?

Does movement training help children jump farther?

Does movement training improve body flexibility?

Participants completed a 6-week movement training program. They took part in 60-minute exercise sessions 2 times a week.

Researchers measured the participants' height, weight, speed, long jump, and flexibility before and after the 6-week training program to see if their physical skills improved.

Studieoversigt

Detaljeret beskrivelse

The aim of this study is to examine the effects of movement training applied during early childhood (ages 6-9) on speed, standing long jump, and flexibility capacity. The study was approved by the Ethics Committee of Istanbul Gelisim University Rectorate with the decision dated 18.03.2026 and numbered 2026-04-42. The study group consisted of 38 individual receiving basic gymnastics training within the Istanbul Gelisim University Sports Club, whose parents provided informed consent. Anthropometric measurements were taken before the training sessions began.

The study lasted for 6 weeks, with training sessions conducted twice a week for 60 minutes. Before and after the training program, participants were tested using the 10-meter sprint test, standing long jump test, and sit-and-reach test. In this study, an experimental method from quantitative research approaches was used, specifically a single-group pretest-posttest design. Data analysis was performed using the SPSS 24 software. The normality of the data was evaluated using the Shapiro-Wilk test, as well as by examining skewness and kurtosis values divided by their standard errors. Following these evaluations, if the data showed a normal distribution, the paired samples t-test was used for two dependent groups. If the data did not show a normal distribution, the nonparametric Wilcoxon Signed Ranks test was applied. In all analyses, a p-value of less than 0.05 was considered statistically significant.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

38

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Barn

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

Children aged between 6 and 9 years

  • Receiving basic gymnastics training at Istanbul Gelisim University Sports Club
  • Having parental/guardian written informed consent
  • Participating in baseline and final outcome measurements

Exclusion Criteria:

Having any physical disability or chronic orthopedic condition that prevents active participation in exercise

  • Missing more than two training sessions during the 6-week program
  • Previous history of acute muscle or joint injury in the past 6 months

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Grundvidenskab
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Movement Education Group
Children aged 6-9 who received basic gymnastics and movement training for 6 weeks (2 days per week, 60 minutes per session)
The program consisted of 60-minute movement and basic gymnastics training sessions conducted 2 times a week over a 6-week period, designed to improve speed, long jump performance, and flexibility.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
10-Meter Sprint Test
Tidsramme: Baseline (Week 0) and Post-intervention (Week 6)
Measured in seconds using a 10-meter sprint test to evaluate the speed capacity of the participants.
Baseline (Week 0) and Post-intervention (Week 6)
Standing Long Jump Test
Tidsramme: Baseline (Week 0) and Post-intervention (Week 6)
Measured in centimeters to assess lower-body explosive power and jump performance
Baseline (Week 0) and Post-intervention (Week 6)
Sit-and-Reach Test
Tidsramme: Baseline (Week 0) and Post-intervention (Week 6)
Measured in centimeters to evaluate lower back and hamstring flexibility.
Baseline (Week 0) and Post-intervention (Week 6)

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Sevinç SERİN YAMAN, PhD, Istanbul Gelisim University

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

4. april 2026

Primær færdiggørelse (Faktiske)

4. juli 2026

Studieafslutning (Faktiske)

4. juli 2026

Datoer for studieregistrering

Først indsendt

26. august 2026

Først indsendt, der opfyldte QC-kriterier

2. september 2026

Først opslået (Faktiske)

3. september 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

3. september 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

2. september 2026

Sidst verificeret

1. september 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 2026-04-42

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Ingen

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