- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT07764913
Effects of Functional Training vs Dual-Task Training in School-Going Children
10 augustus 2026 bijgewerkt door: Riphah International University
Effects of Progressive Functional Training Versus Dual-Task Performance in School-Going Children
This study aims to compare the effects of Progressive Functional Training and Dual-Task Training on motor skills in school-going children.
It focuses on improving balance, coordination, strength, and motor-cognitive integration.
A randomized clinical trial will be conducted on children aged 6-12 years divided into two groups receiving different interventions for 4 weeks.
Studie Overzicht
Toestand
Voltooid
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
Motor skill development during childhood plays a vital role in physical fitness, academic participation, and overall functional independence.
School-going children require adequate motor competence to perform daily activities, participate in sports, and adapt to increasingly complex physical and cognitive demands.
Traditional physical education programs often focus on isolated physical skills, which may not fully address real-life multitasking requirements.
Progressive functional training (PFT) emphasizes task-oriented, developmentally appropriate movements that mimic daily activities and progressively increase in difficulty.
This approach helps improve fundamental motor skills, balance, coordination, and strength.
In contrast, dual-task training (DTT) involves the simultaneous performance of motor and cognitive tasks, thereby enhancing motor performance under divided attention and improving motor-cognitive integration.
Although both training methods have shown positive effects on motor skills, limited evidence exists comparing their effectiveness in school-going children.
Therefore, this study aims to compare the effects of progressive functional training versus dual-task training on motor skills in school-going children.
This study will adopt a randomized clinical design.
A total of 66 school-going children aged 6-12 years will be selected based on predefined inclusion and exclusion criteria.
Participants will be randomly allocated into two groups: Group A (Progressive Functional Training) and Group B (Dual-Task Training).
Baseline assessments of motor skills will be conducted using standardized tools such Bruin inks- as the Ossietzky Test of Motor Proficiency (BOT-2), Pediatric Balance Scale, and Dual-Task Timed Up and Go Test.
Group A will undergo progressive functional training focusing on balance, coordination, strength, and functional movement patterns.
Group B will receive dual-task training involving motor activities combined with cognitive tasks.
Both groups will receive training for 4 weeks, with sessions conducted 3 times per week.
Post-intervention assessments will be performed using the same outcome measures.
The collected data will be statistically analyzed to compare pre- and post test outcomes within and between groups.
Studietype
Ingrijpend
Inschrijving (Werkelijk)
66
Fase
- Niet toepasbaar
Contacten en locaties
In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.
Studie Locaties
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54660
- Riphah International University
-
-
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
Accepteert gezonde vrijwilligers
Ja
Beschrijving
Inclusion Criteria:
- School going children aged 6-12 years ,
- Both gender ,Ability to understand and follow simple verbal instruction ,
- Typically developing children
Exclusion Criteria:
- Visual or hearing issue ,
- Recent injury or surgeries
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Progressive Functional Training Group
This program involves task-oriented exercises such as sit-to-stand, step-ups, reaching, jumping, and obstacle walking, with progressive increases in difficulty, speed, and resistance.
It is performed for 30-40 minutes per session, three times per week for six weeks, including a 5-7 minute warm-up, 30 minutes of functional training, and a 5-8 minute cool-down.
Training progresses from low-intensity activities in weeks 1-2 (e.g., sit-to-stand, walking, low step-ups, ball activities, and static balance) to moderate intensity in weeks 3-4 (e.g., squats with reach, tandem and obstacle walking, ball tasks, and dynamic balance), and high intensity in weeks 5-6 (e.g., lunges, jumping, agility drills, direction changes, and advanced balance tasks).
|
This program involves task-oriented exercises such as sit-to-stand, step-ups, reaching, jumping, and obstacle walking, with progressive increases in difficulty, speed, and resistance.
It is performed for 30-40 minutes per session, three times per week for six weeks, including a 5-7 minute warm-up, 30 minutes of functional training, and a 5-8 minute cool-down.
Training progresses from low-intensity activities in weeks 1-2 (e.g., sit-to-stand, walking, low step-ups, ball activities, and static balance) to moderate intensity in weeks 3-4 (e.g., squats with reach, tandem and obstacle walking, ball tasks, and dynamic balance), and high intensity in weeks 5-6 (e.g., lunges, jumping, agility drills, direction changes, and advanced balance tasks).
|
|
Actieve vergelijker: Dual Task Performance Group
This program combines motor and cognitive tasks, such as walking while counting, balance with memory recall, and ball activities with verbal tasks, with gradually increasing cognitive complexity.
It is performed for 30-40 minutes per session, three times per week for six weeks, to improve dual-task performance, attention, and executive function.
Each session includes a 5-7 minute warm-up, followed by 30 minutes of dual-task training progressing from simple tasks (e.g., walking while counting forward, naming animals during balance) to moderate (e.g., counting backward, obstacle walking with naming tasks) and then complex activities (e.g., direction-change walking while counting by threes, hopping with verbal tasks, TUG with cognitive tasks).
Sessions end with a 5-8 minute cool-down of relaxed walking, stretching, and breathing exercises.
|
This program combines motor and cognitive tasks, such as walking while counting, balance with memory recall, and ball activities with verbal tasks, with gradually increasing cognitive complexity.
It is performed for 30-40 minutes per session, three times per week for six weeks, to improve dual-task performance, attention, and executive function.
Each session includes a 5-7 minute warm-up, followed by 30 minutes of dual-task training progressing from simple tasks (e.g., walking while counting forward, naming animals during balance) to moderate (e.g., counting backward, obstacle walking with naming tasks) and then complex activities (e.g., direction-change walking while counting by threes, hopping with verbal tasks, TUG with cognitive tasks).
Sessions end with a 5-8 minute cool-down of relaxed walking, stretching, and breathing exercises.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Bruininks-Oseretsky Test of Motor Proficiency
Tijdsspanne: The BOT-2 Short Form was administered at baseline and after the 6-week intervention. Each assessment required approximately 15-20 minutes to complete.
|
Bruininks-Oseretsky Test of Motor Proficiency Used for composites and overall proficiency, ranging from a scale of 20 to 80 .
Assesses gross and fine motor skills Subtests include: Balance, running, speed and agility, Bilateral coordination, Strength Suitable for children aged 4-21 years, widely used, reliable, and valid for school aged children
|
The BOT-2 Short Form was administered at baseline and after the 6-week intervention. Each assessment required approximately 15-20 minutes to complete.
|
|
digit span test
Tijdsspanne: Time Frame: Assessed at baseline (Week 1) and after 6 weeks of intervention (Week 6).
|
This framework assesses fundamental motor skills in children aged 3-10, including locomotor skills (running, jumping, hopping) and object control skills (throwing, catching, kicking), commonly used in school-based interventions.
Cognitive dual-task performance is measured using the Digit Span Test (forward and backward) to assess attention and working memory during concurrent motor tasks, and the Verbal Fluency Test (animal naming) to evaluate executive function and cognitive flexibility, with outcomes based on correct recall sequences and number of words generated in 60 seconds.
|
Time Frame: Assessed at baseline (Week 1) and after 6 weeks of intervention (Week 6).
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Onderzoekers
- Hoofdonderzoeker: Hafsa Aslam, MS-PT, Riphah International University
Publicaties en nuttige links
De persoon die verantwoordelijk is voor het invoeren van informatie over het onderzoek stelt deze publicaties vrijwillig ter beschikking. Dit kan gaan over alles wat met het onderzoek te maken heeft.
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start (Werkelijk)
16 april 2026
Primaire voltooiing (Werkelijk)
5 juli 2026
Studie voltooiing (Werkelijk)
10 juli 2026
Studieregistratiedata
Eerst ingediend
5 mei 2026
Eerst ingediend dat voldeed aan de QC-criteria
10 augustus 2026
Eerst geplaatst (Werkelijk)
14 augustus 2026
Updates van studierecords
Laatste update geplaatst (Werkelijk)
14 augustus 2026
Laatste update ingediend die voldeed aan QC-criteria
10 augustus 2026
Laatst geverifieerd
1 augustus 2026
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Andere studie-ID-nummers
- REC/RCR&AHS/25/0769
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
NEE
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Nee
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Nee
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .