AzTrials
AzTrials

Cerebral Palsy, HemiplegicNCT07429175

Sensory-Motor Relationship in Unilateral CP

An observational study of Cerebral Palsy, Hemiplegic, run by Ankara University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Cerebral palsy (CP) is characterized by many problems related to brain damage. One of these is sensory impairment. Sensory impairments in CP patients can also occur together with motor functions. Read more about this study

Who is it for?
Ages 6 to 15 yearsHealthy volunteers can take part
Conditions the study is for
Cerebral Palsy, Hemiplegic
How many people
110 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Sep 2024to 30 Nov 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 15 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Study population: Children with unilateral cerebral palsy (CP) who meet the inclusion criteria and who apply to the Physical Medicine and Rehabilitation Department Clinic or Outpatient Clinic of Ankara University Faculty of Medicine, as well as healthy volunteers, will be included in the study.

Who may be able to join

  • Children aged 15 with unilateral cerebral palsy (CP)
  • Being between Gross Motor Functional Classification System I-IV
  • Not having undergone surgery or botulinum toxin application to the affected upper extremity in the last 6 months
  • Understanding what is said and being able to follow commands
  • The patient or their relatives having completed an informed consent form

Who cannot join

  • Having a neurological disease affecting the motor and sensory system other than cerebral palsy
  • The participant having a dermatological, vascular, or orthopedic problem in the upper extremity that would prevent assessment
  • Having uncorrected vision and hearing problems
  • Having autism spectrum disorder and attention deficit hyperactivity disorder
  • Having insufficient intelligence level

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Ankara University, Faculty of Medicine

    Ankara

Other trials in Turkey (Türkiye)

About this study

Official title: The Relationship Between Sensory Impairments and Upper Extremity Motor Functions in Children With Unilateral Cerebral Palsy

Cerebral palsy (CP) is characterized by many problems related to brain damage. One of these is sensory impairment. Sensory impairments in CP patients can also occur together with motor functions. Detecting sensory impairments (two-point discrimination, vibration, joint position sense, thermal sensation, stereognosis, graphesthesia) in the arm, forearm, and hand (upper extremity) in CP patients and investigating their relationship with motor functions is important. The aim of this research is to investigate the relationship between upper extremity sensory impairments and motor functions in patients diagnosed with unilateral (affecting one half of the body) CP.

Read the detailed description

The aim of this study is to investigate the relationship between sensory impairments and upper extremity motor functions in patients with unilateral cerebral palsy (CP). It will be planned as a cross-sectional study. The study will include 55 unilateral CP patients and 55 healthy volunteers. Sensory functions evaluated include two-point discrimination, joint position sense, vibration sense, thermal sense, stereognosis, and graphesthesia. Motor functions will be assessed using the Gross Motor Functional Classification System (GMFSS), Hand Skills Classification System (ESCS), Abilhand-Kids scale, Box and Block test, and Nine Hole Peg test. The relationship between sensory parameters and motor functions will be investigated.

Keywords
cerebral palsy, sensory function, motor function
Medical subject headings
Cerebral Palsy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07429175
Study groupRoleWhat they receive
Patient GroupChildren aged 6-15 with unilateral (hemiplegic) cerebral palsy
Healthy GroupHealthy children aged 6-15

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Sensory Function:Two-point discrimination

    Two-point discrimination is defined as the ability to distinguish between two simultaneous points of touch, which is most acute in areas of the skin with a high density of touch receptors, such as the fingers and face. The test will be performed using a discriminator device called an esthesiometer.

    Measured: Single assessment at baseline (cross-sectional evaluation)

  2. Sensory Function:Joint position sense

    Joint position sense is the ability to detect body segment position in space and is commonly used to represent proprioceptive performance.

    Measured: Single assessment at baseline (cross-sectional evaluation)

  3. Sensory Function:Vibration

    Assessment of vibration sense is the best clinical test of the dorsal column pathway. A low-frequency (128 Hz) tuning fork is applied to bony prominences and the patient (with closed eyes) is asked to report when the vibration starts and stops.

    Measured: Single assessment at baseline (cross-sectional evaluation)

  4. Sensory Function:thermal sense

    The volunteer's upper extremity is successively touched with tubes filled with hot and cold water, and the volunteer is asked to respond as hot or cold. Thermal sensation is recorded as 'preserved', 'impaired', or 'unable to assess'.

    Measured: Single assessment at baseline (cross-sectional evaluation)

  5. Sensory Function:Stereognosis

    Without visual or auditory cues, objects are placed in a sequence, and the child is asked to grasp them and identify the name of the object. Each object is awarded '1' point for being correctly identified, and '0' points for not identifying it. Scores ranging from 0 to 6 are recorded.

    Measured: Single assessment at baseline (cross-sectional evaluation)

  6. Sensory Function:Graphesthesia

    Six different drawings-letters, numbers, circles, and vertical lines-are made on the palm of the volunteer's hand using a blunt pencil, without any visual or auditory stimuli. Each correct drawing earns '1' point, and each incorrect drawing earns '0' points. Scores ranging from 0 to 6 are recorded.

    Measured: Single assessment at baseline (cross-sectional evaluation)

  7. Motor Function: Gross Motor Functional Classification System

    This classification system consists of 5 levels.

    Measured: Single assessment at baseline (cross-sectional evaluation)

  8. Motor Function: Hand Skills Classification System

    This classification system consists of 5 levels.

    Measured: Single assessment at baseline (cross-sectional evaluation)

  9. Motor Function: Abilhand-Kids Scale

    Twenty-one daily activities were evaluated. Participants were asked to rate an activity-which the child attempted to perform independently using both upper extremities-on a scale of 0-42 points.

    Measured: Single assessment at baseline (cross-sectional evaluation)

  10. Motor Function: Nine Hole Peg Test

    The Nine Hole Peg Test was developed to measure finger dexterity, also known as fine manual dexterity. The test consists of a wooden board with nine holes and nine small sticks designed to be inserted into those holes. The participant is asked to take the sticks from the box one by one with the hand being tested and insert them into the holes as quickly as possible; then, they must remove the sticks one by one and return them to the box.

    Measured: Single assessment at baseline (cross-sectional evaluation)

  11. Motor Function: Box and Block Test

    The Box and Block Test (BBT) measures unilateral gross manual dexterity. Participants are given 60 seconds to move wooden blocks by hand to the opposite compartment as quickly as possible. At the end of 60 seconds, the number of wooden blocks transferred to the opposite compartment is noted.

    Measured: Single assessment at baseline (cross-sectional evaluation)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Feb 2026
  2. Study start1 Sep 2024
  3. Primary completion30 Nov 2025
  4. Study completion30 Nov 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
110 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07429175
Sponsor's protocol ID
İ07-512-24
Status last verified
Feb 2026
First submitted
27 Jan 2026
Last updated
24 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Cerebral Palsy, Hemiplegic, run by Ankara University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Sensory Function:Two-point discrimination (time frame: Single assessment at baseline (cross-sectional evaluation)). The study lists 11 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Feb 2026; AzTrials last refreshed its copy on 6 Nov 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in