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Recruiting NCT06974890

NCT06974890 Effects of Shuttle Balance Training on Balance , Gait and Postural Control in Children With Mild Cognitive Impairment

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Clinical Trial Summary
NCT ID NCT06974890
Status Recruiting
Phase —
Sponsor Riphah International University
Condition Mild Cognitive Impairment
Study Type INTERVENTIONAL
Enrollment 24 participants
Start Date 2025-04-15
Primary Completion 2025-06-30

Eligibility & Interventions

Sex All sexes
Min Age 6 Years
Max Age 12 Years
Study Type INTERVENTIONAL
Interventions
Shuttle Balance TrainingBaseline Treatment

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 24 participants in total. It began in 2025-04-15 with a primary completion date of 2025-06-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study aims to investigate the impact of Shuttle Balance Training (SBT) on balance, gait, and postural control among children diagnosed with mild cognitive impairment (MCI). Mild cognitive impairment in children often manifests as challenges in cognitive processing, motor coordination, and daily activities that involve balance and movement. The research will employ a randomized controlled trial (RCT) design, involving children aged 6-12 years diagnosed with MCI. Participants will be randomly assigned to either an experimental group receiving Shuttle Balance Training or a control group receiving standard care or placebo interventions. The Shuttle Balance Training protocol consists of structured sessions focusing on dynamic balance exercises, coordination drills, and proprioceptive challenges using shuttle devices. Training sessions will be conducted thrice weekly over a period of 12 weeks, with each session lasting approximately 45 minutes. The study will be randomized controlled trial. Total \_\_ subjects will be assigned by non probability convenient sampling technique. They were randomly assigned to experimental and control groups. The Berg balance scale, limits of stability test, GOAL test, Timed up and go tools will be used. Tests will be used as outcome measure tools for balance, walk, coordination and Physical activity. All measures will be taken at baseline and at the end of treatment session. The collected data will be analyzed in Statistical Package for the Social Sciences (SPSS) 25.0 version. If data will be normally distributed then parametric if not normally distributed than non-parametric test will be apply.

Eligibility Criteria

Inclusion Criteria: Children with mild cognitive impairment (50-70%IQ) * Age group from 6 to 12 years * Both male and female * Children must have the physical and cognitive ability to engage in the activities * Children should be in generally good health, without severe medical conditions or orthopedic issues Exclusion Criteria: * Children with severe cognitive impairment * Children who have severe neurological disorders * Children with visual and auditory impairment * Children with severe sensory processing disorders

Contact & Investigator

Central Contact

: IMRAN AMJAD, PhD

✉ imran.amjad@riphah.edu.pk

📞 9233224390125

Principal Investigator

ZAHRA AHMAD, MS-PPT

PRINCIPAL INVESTIGATOR

Riphah International University

Frequently Asked Questions

Who can join the NCT06974890 clinical trial?

This trial is open to participants of all sexes, aged 6 Years or older, up to 12 Years, studying Mild Cognitive Impairment. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06974890 currently recruiting?

Yes, NCT06974890 is actively recruiting participants. Contact the research team at imran.amjad@riphah.edu.pk for enrollment information.

Where is the NCT06974890 trial being conducted?

This trial is being conducted at Lahore, Pakistan.

Who is sponsoring the NCT06974890 clinical trial?

NCT06974890 is sponsored by Riphah International University. The principal investigator is ZAHRA AHMAD, MS-PPT at Riphah International University. The trial plans to enroll 24 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology