3D-Printed seat aims to boost daily life for kids with movement disorders
NCT ID NCT07330921
First seen Jun 27, 2026 · Last updated Jul 14, 2026 · Updated 2 times
Summary
This study tests a new 3D-printed seating system (SSAP3D) designed for children aged 2-6 with neuromotor dysfunction. The goal is to see if the custom seat improves their ability to perform daily activities and participate at home, school, and in the community. Twelve children will try both the new seat and their usual seating system for six weeks each, and families will report on changes in function and quality of life.
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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 12 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Apr 2026
- Expected to finish
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Oct 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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2 to 6 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: * Medical Situation of Neuromotor Disfunction * Be user of some type of adapted seating system * Age between 2-6 years * Have head control levels of 3 to 8 on the Level of Sitting Scale (LSS) * Be able to maintain a standing position for at least 10 seconds, with or without external assistance. Exclusion Criteria: * Presenting moderate or severe cognitive impairment, which generates significant difficulties in understanding the instructions given by the evaluator * Having suffered a traumatic injury o surgical process in the 6 months prior to the start of the study or during the study
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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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AIDIMO (Asociación para la Investigación en la Discapacidad Motriz)
RECRUITINGZaragoza, Zaragoza, 50011, Spain