Wearable sensors give Real-Time feedback to improve gait in children with hemiplegia
NCT ID NCT07683624
First seen Jul 06, 2026 · Last updated Jul 07, 2026 · Updated 1 time
Summary
This trial tests whether a biofeedback system using wearable sensors can improve walking in children aged 7 to 12 with hemiplegia (weakness on one side). Participants wear sensors that provide real-time audio and visual cues while walking on a treadmill, helping them correct abnormal gait patterns. The study compares this approach to conventional physical therapy over three months, measuring changes in step time, stride length, and other walking parameters.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Steadys Biofeedback Gait Training System
- What this could lead to
- If effective, this approach could offer a more engaging and targeted way to improve walking patterns in children with hemiplegia, potentially enhancing mobility and independence.
- What could go wrong
- This is a small, early-stage trial with only 30 participants, so results may not apply to all children. The biofeedback system may not lead to significantly better outcomes than standard therapy.
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 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
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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7 to 12 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: * Their age will range from 7 to 12 years. * The degree of their spasticity will range from 1 to 1+ according to Modified Ashworth' Scale (Bohannon et al., 1987) (Appendix IⅠ). * They will be on level Ⅰ or Ⅱ on GMFCS (Palisano et al., 2007) (Appendix IⅡ). * They will be able to walk without the use of an assistive device * Children can follow instructions and understand given orders. Exclusion Criteria: * Severe visual or hearing impairment. * Fixed deformities or surgical interventions in the lower extremities. * Botulinum toxin injections in the last 6 months.
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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
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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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.
Contacts and locations
Locations
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Faculty of Physical Therapy Cairo University
Cairo, 11351, Egypt
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Other studies related to the condition(s) this trial covers.
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- Can watching or mirroring movements strengthen Children's hands?
- Mirror illusion may help children with cerebral palsy regain arm control