Clinical effects of upper limb rehabilitation robot training in children and adolescents with cerebral palsy

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0010831

Enrollment

Registered

2025-07-30

Start date

2025-07-28

Completion date

Unknown

Last updated

2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device : Participants will receive upper limb rehabilitation training for 30 minutes per session, three times a week, for a total of 8 weeks. The rehabilitation methods will be randomly assign

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: ? Children and adolescents with cerebral palsy classified as Levels I to IV on the Manual Ability Classification System (MACS). ? Children with cerebral palsy classified as Levels I to IV on the Gross Motor Function Classification System (GMFCS), who are able to maintain a sitting position independently or with assistance for at least 30 minutes. ? Participants with sufficient cognitive ability to understand and follow instructions. ? Aged 4 years or older and under 18 years. ? Participants (and/or their legal guardians) who voluntarily agree to participate in the clinical trial and provide written informed consent.

Exclusion criteria

Exclusion criteria: ? Participants with intellectual disabilities to the extent that they are unable to follow instructions during the use of the upper limb rehabilitation robot. ? Participants with significant visual impairments that make it impossible to recognize images on the screen during robotic training. ? Participants with skin or musculoskeletal conditions that prevent them from wearing or using the upper limb rehabilitation device. ? Any other individuals whom the investigator judges to be unsuitable for participation in the study.

Design outcomes

Primary

Measure	Time frame
Shriners Hospital Upper Extremity Evaluation (SHUEE)	—

Secondary

Measure	Time frame
Upper limb function assessment (9 hole pegboard, box & block test);Upper limb muscle strength assessment (grasp power, pinch power);Assessment of upper limb spasticity and joint contracture severity(Modified Ashworth Scale, Modified Tardieu Scale);Activities of Daily Living Assessment (Pediatric Motor Activity Log);Assessment of visual perception function(Motor-Free Visual Perception Test-Fourth Edition);Assessment of frontal lobe activation (Functional Near-Infrared Spectroscopy)	—

Measure

Time frame

Upper limb function assessment (9 hole pegboard, box & block test);Upper limb muscle strength assessment (grasp power, pinch power);Assessment of upper limb spasticity and joint contracture severity(Modified Ashworth Scale, Modified Tardieu Scale);Activities of Daily Living Assessment (Pediatric Motor Activity Log);Assessment of visual perception function(Motor-Free Visual Perception Test-Fourth Edition);Assessment of frontal lobe activation (Functional Near-Infrared Spectroscopy)

—

Countries

Korea, Republic of

Contacts

Public ContactSo Jung Kwon

Chungnam National University Hospital

thwjd7081@gmail.com+82-2-338-2987

Outcome results