Effects Of Spiral Strapping Systems On Upper Limb Function In Unilateral Spastic Cerebral Palsy (NCT07418710) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effects Of Spiral Strapping Systems On Upper Limb Function In Unilateral Spastic Cerebral Palsy
27 participantsStarted 2026-02-15
Plain-language summary
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.
Who can participate
Age range
4 Years – 15 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
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
Exclusion Criteria:
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.