Effects Of Spiral Strapping Systems On Upper Limb Function In Unilateral Spastic Cerebral Palsy

Starting soon · Not applicable

Conditions studied: Cerebral Palsy (CP), Hand Grip Strength, Upper Extremity Function, Spasticity

In brief

The purpose of this clinical study is to learn whether two different spiral strapping systems can improve arm and hand use in children with unilateral spastic cerebral palsy. These strapping systems are used to support the arm in a more functional position and to help children control their movements during daily activities. This study aims to answer the following main questions: Does spiral strapping help children use their arm and hand more effectively in daily activities? Does spiral strapping improve hand skills and grip strength? Is there a difference in effect between the two spiral strapping systems? To answer these questions, researchers will divide participants into three groups. One group will receive a standard rehabilitation program plus TheraTogs® spiral strapping. A second group will receive the same rehabilitation program plus TogRite™ spiral strapping. The third group will receive the rehabilitation program only. Participants will: Take part in rehabilitation sessions twice a week for eight weeks. Use spiral strapping during some sessions, depending on their group. Complete arm and hand assessments at the beginning and at the end of the study. The results of this study may help develop simple and practical rehabilitation approaches that support children with cerebral palsy in becoming more independent in daily life.

Key facts

Study ID

NCT07418710

Run by

Abant Izzet Baysal University

People needed

27

Starts

2026-02-15

Expected to finish

2027-02-15

Last updated by the study team

2026-02-18

Who can join

Age: 4 and older, up to 15. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Diagnosis of unilateral spastic cerebral palsy
• Age between 4 and 15 years
• Manual Ability Classification System (MACS) levels I-III
• Presence of spasticity graded as 1, 1+, or 2 on the Modified Ashworth Scale in at least two of the following upper limb muscle groups: shoulder internal rotators, elbow flexors, forearm pronators, wrist flexors, finger flexors, or thumb adductors
• Communication Function Classification System (CFCS) levels I-II
• Gross Motor Function Classification System (GMFCS) levels I-III
• Ability to actively participate in upper limb rehabilitation interventions
• Written informed consent provided by parents or legal guardians

You may not qualify if…

• Upper limb botulinum toxin injection or upper limb surgery within the last 6 months
• Presence of fixed contractures in the upper limb joints that may interfere with assessment or intervention protocols
• Severe behavioral or communication problems that would prevent participation in the study procedures
• Uncontrolled or treatment-resistant epilepsy

Full record on ClinicalTrials.gov

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