Actively Recruiting

Age: 6Years - 15Years
All Genders
Healthy Volunteers
NCT07352735

Upper Extremity Sensation and Function in Children With Cerebral Palsy

Led by Abant Izzet Baysal University · Updated on 2026-02-03

24

Participants Needed

1

Research Sites

43 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This cross-sectional study was designed to evaluate upper extremity sensation in children with spastic cerebral palsy and to investigate its effect on upper extremity use in activities of daily living. Children aged 6-15 years with cerebral palsy (n=12) and typically developing peers (n=12) who volunteer to participate in the study will be included. Participants' sociodemographic data will be recorded, and upper extremity vibration sense, stereognosis, tactile sense, two-point discrimination, and joint position sense will be assessed. In the final stage, the Jebsen Taylor Hand Function Test will be administered, and parents will be asked to complete the Abilhand Kids Hand-Related Ability Scale.

CONDITIONS

Official Title

Upper Extremity Sensation and Function in Children With Cerebral Palsy

Who Can Participate

Age: 6Years - 15Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Have a diagnosis of Cerebral Palsy (for cerebral palsy group)
  • Be between 6 and 15 years old
  • Volunteer to participate in the study
  • Be typically developing (for control group)
Not Eligible

You will not qualify if you...

  • Have spasticity that limits active wrist movements
  • Have had botulinum toxin injections or surgery involving upper extremities within the last 6 months
  • Refuse to participate in the study
  • Have a history of upper extremity injury or dysfunction
  • Have a mental disability

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Bolu abant Izzet Baysal University

Bolu, Turkey (Türkiye), 14030

Actively Recruiting

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Research Team

S

Sezen Tezcan

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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