Simple straps may boost hand skills in kids with cerebral palsy
NCT ID NCT07418710
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests two types of spiral arm straps (TheraTogs and TogRite) to see if they help children with unilateral spastic cerebral palsy use their affected arm and hand more effectively. Twenty-seven children aged 4 to 15 will be split into three groups: one gets rehab plus TheraTogs, another gets rehab plus TogRite, and the third gets rehab alone. Over eight weeks, researchers will measure grip strength, dexterity, and movement quality to compare the approaches.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- TheraTogs® Spiral Strapping System and TogRite™ Spiral Strapping System (supportive braces)
- What this could lead to
- If successful, these strapping systems could offer a simple, low-cost way to help children with cerebral palsy use their affected arm and hand more effectively in daily activities.
- What could go wrong
- This is a very small, early-stage study (27 children) with no blinding, so results may not be generalizable. The devices only provide temporary support and are not a cure.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 27 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Feb 2026
An estimate. Start dates often move.
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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4 to 15 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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