NCT07287215

Brief Summary

The main purpose of this study was to examine the relationship between motor imagery capacity and functional mobility, walking and balance in children with diplegic type cerebral palsy.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
99

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Nov 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 24, 2025

Completed
8 days until next milestone

First Submitted

Initial submission to the registry

December 2, 2025

Completed
15 days until next milestone

First Posted

Study publicly available on registry

December 17, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 23, 2026

Completed
3 days until next milestone

Study Completion

Last participant's last visit for all outcomes

February 26, 2026

Completed
Last Updated

December 17, 2025

Status Verified

December 1, 2025

Enrollment Period

3 months

First QC Date

December 2, 2025

Last Update Submit

December 16, 2025

Conditions

Outcome Measures

Primary Outcomes (5)

  • Mental Stopwatch Paradigm

    A mental stopwatch will be used to assess explicit MI capacity. This paradigm compares the time between the actual movement duration and the duration of a similar imagined task.

    24-48 hours

  • Laterality Task (Choice Task):

    Laterality Task (Choice Task): Implicit Motor Imagery capacity will be measured through a laterality task, which involves deciding which side a limb belongs to. Right-left discrimination of the foot will be assessed using the "Recognize Foot" application developed by the Neuro Orthopaedic Institute

    24-48 hours

  • Functional Mobility using the Functional Mobility Scale (FMS)

    Functional Mobility: Functional Mobility will be assessed using the Functional Mobility Scale (FMS)

    24-48 hours

  • Functional Mobility using the Timed Up and Go test

    Functional Mobility: Functional Mobility will be assessed using the Timed Up and Go test.

    24-48 hours

  • The Gillette Functional Assessment Questionnaire

    Gait assessment: The Gillette Functional Assessment Questionnaire is a self- or observer-based assessment tool, minimum score 22 maximum score 88

    24-48 hours

Interventions

Laterality Task (Choice Task): Implicit Motor Imagery capacity will be measured through a laterality task, which involves deciding which side a limb belongs to. Right-left discrimination of the foot will be assessed using the "Recognize Foot" application developed by the Neuro Orthopaedic Institute

A mental stopwatch will be used to assess explicit MI capacity. This paradigm compares the time between the actual movement duration and the duration of a similar imagined task.

Functional Mobility: Functional Mobility will be assessed using the Functional Mobility Scale (FMS) and the Timed Up and Go test.

Gait assessment: The Gillette FDA is a self- or observer-based assessment tool.

Eligibility Criteria

Age5 Years - 18 Years
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64)
Sampling MethodNon-Probability Sample
Study Population

diplegic cerebral palsy

You may qualify if:

  • Diagnosed with diplegic CP by a neurologist or pediatric neurologist
  • Being between 5 and 18 years of age
  • Being between levels I and III on the GMFCS
  • Having the cognitive ability to follow the assessment instructions
  • Informed consent form has been obtained from the child's family
  • The child has agreed to participate voluntarily in the study

You may not qualify if:

  • Having severe impairments in basic sensory systems such as vision or hearing
  • Having additional diagnoses such as epilepsy or autism spectrum disorder
  • Demonstrating cognitive or behavioral problems that prevent them from following instructions during the assessment
  • Having informed consent from the child's family or the child

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Bingöl

Bingöl, Turkey (Türkiye)

RECRUITING

Central Study Contacts

dilan demirtas karaoba, asst. prof, asst. prof

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
assistant professor

Study Record Dates

First Submitted

December 2, 2025

First Posted

December 17, 2025

Study Start

November 24, 2025

Primary Completion

February 23, 2026

Study Completion

February 26, 2026

Last Updated

December 17, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations