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CompletedNCT07045922Updated Oct 27, 2026

Motor-Cognitive Training , Cognitive Performance and Balance

An interventional study of Motor-Cognitive Training Program and Regular Physical education classes in Coordination Impairment, Children and Balance, sponsored by Princess Nourah Bint Abdulrahman University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 10 Years to 12 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-27.

Sponsored by Princess Nourah Bint Abdulrahman University · Not applicable, Interventional, and Treatment

Updated Oct 27, 2026Eligibility revisedGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
10 Years to 12 Years
Sex
All
01

Study summary

This RCT design investigates the effects of an 8-week motor-cognitive training program on cognitive performance and balance in preschool-aged children. Participants in the intervention group received structured motor-cognitive activities twice a week in addition to their regular physical education (PE) classes. The control group attended only standard PE classes and was restricted from participating in any other physical activity. Assessments included cognitive testing (Go/No-Go, Tower of Hanoi, and Corsi Block), anthropometric measurements, and static/proprioceptive balance testing. All measurements were conducted pre- and post-intervention.

02

Conditions studied

  • Coordination Impairment
  • Children
  • Balance

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03

In context

Ataxia

149 studies on the registry are indexed under Ataxia; 37 are open to participants now.

This study's enrollment of 50 is above the median of 30 across 100 interventional studies indexed under Ataxia.

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Lead sponsor

Princess Nourah Bint Abdulrahman University is the lead sponsor of 31 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
10 Years to 12 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Typically developing preschool-aged children
  • Able to follow basic instructions
  • Parental/guardian consent obtained

Exclusion criteria

Exclusion Criteria:

  • Diagnosed neurodevelopmental disorders
  • Recent musculoskeletal injuries
  • Participation in other structured physical activity programs
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
50 participants (actual)

Study arms

  • Experimental
    Motor-Cognitive Training Program

    • Motor-Cognitive Training Program: Game-based physical activities targeting cognitive and motor domains (e.g., running drills, hand skills, stability tasks). Exercises progressed weekly in complexity and duration. Sessions lasted 25-30 minutes, twice weekly.

    Behavioral: Motor-Cognitive Training Program · Other: Regular Physical education classes

  • Other
    Regular Physical education

    • Regular PE classes only; no additional physical or motor training permitted.

    Other: Regular Physical education classes

Interventions

  • BehavioralMotor-Cognitive Training Program

    Participants assigned to the intervention group participated in a structured motor-cognitive training program in addition to their regular physical education (PE) classes. The training was designed to integrate physical movement with cognitive engagement in a game-based format, suitable for the preschool age group. The program was conducted twice weekly for eight weeks, with each session lasting approximately 25-30 minutes. Activities progressed in complexity over time, incorporating elements of motor planning, executive functioning, and balance control. Sessions consisted of: Warm-up phase: Light aerobic activities such as jogging, dynamic stretching, and coordination drills (e.g., knee pulls, toe walking). Main training phase: Activities targeting core cognitive-motor domains l

  • OtherRegular Physical education classes

    Participants in the control group continued with their regularly scheduled physical education (PE) classes as mandated by the school curriculum. They did not receive any additional motor-cognitive or structured exercise training. Furthermore, they were instructed not to engage in any external physical activity programs outside of the regular PE sessions throughout the study duration. This restriction was monitored to ensure group consistency.

06

What researchers measure

Primary outcomes

  1. Cognitive Function Tests

    Evaluates inhibitory control, a core component of executive functioning. Participants are required to respond quickly to target stimuli (e.g., "X") while inhibiting responses to non-target stimuli (e.g., "O"). Measures include: Number of correct responses (go trials) Number of commission errors (false responses to no-go trials) Reaction time (latency) to correct go stimuli Duration: \~5 minutes and 40 seconds

    Time frame: Administered at baseline (pre-intervention) and 8 weeks (post-intervention)

  2. Tower of Hanoi Test executive functioning

    Assesses executive functioning, including planning, problem-solving, and cognitive flexibility. Participants solve a visual puzzle by moving disks across pegs, following specific rules. Performance variables include: * Number of moves to solution * Total task completion time * Average time per move * Latency to first move (planning time)

    Time frame: Baseline and 8 weeks

  3. Balance Performance

    Balance was assessed using the Sensbalance MiniBoard, a validated interactive platform that captures both static and proprioceptive balance. Two types of balance tasks were used: Static Balance Test: Participants were instructed to maintain a stable position on the balance board while keeping a ball centered within a visual target zone on the screen. The performance level (%) was calculated using the formula: (1 - Measured Sway Amplitude / Maximum Allowable Sway) × 100, indicating the participant's ability to maintain balance within defined limits.

    Time frame: Baseline and 8 weeks

07

Study locations

1 site
  • Tekirdağ Namik Kemal University
    Tekirdağ, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Eligibility
Minimum age 2 Years→10 Years; Maximum age 6 Years→12 Years
Oct 27, 2026
Show all 1 update
  1. Oct 27, 2026
    Eligibility Minimum age 2 Years→10 Years; Maximum age 6 Years→12 Years
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07045922
Lead sponsor
Princess Nourah Bint Abdulrahman University
Responsible party
Monira Aldhahi (Associate Prof, Princess Nourah Bint Abdulrahman University) — Principal investigator
First posted
Jul 1, 2025
Start date
Jun 30, 2025
Primary completion
Nov 30, 2025
Completion
Dec 1, 2025
Last update
Oct 27, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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