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Research summary · 11 d ago

AI summary · not yet reviewedSubjects not reportedInterventionalTrial registry record – peer review not applicable

Study of NEUROSWING Orthosis in Animal/Cell Models

An interventional study was conducted to evaluate the NEUROSWING Orthosis, a carbon orthosis with an active ankle articulation, comparing it to a control carbon orthosis. The primary endpoint was walking speed measured by a 10m walk test, with 34 subjects planned for assessment over 12 visits from baseline to day 35.

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This plain-English summary was written by AI from a trial registry record and may contain errors. It is not medical advice. Read the original study and talk to your MS team before making decisions about treatment.

Human efficacy: Not yet assessed
Mechanism: Not yet assessed
Evidence strength: Not yet assessed
Outcome: Not yet assessed

Why it matters

Understanding the efficacy of the NEUROSWING Orthosis could inform future designs of orthotic devices aimed at improving mobility in individuals with multiple sclerosis and related conditions.

What this does not prove

No results are available, making it impossible to assess the efficacy of the intervention. The information provided reflects only planned study parameters, not actual findings or outcomes.

Next milestone

No next milestone was established from the available source.

Study facts

Study design: Interventional
Participants / samples: 34 · basis not reported
Randomised: Yes
Controlled: Yes
Primary endpoint met: Not reported
Relevant MS type: All
Publication date: Not reported
Evidence reviewed: Trial registry record
Regulatory approval: No
Research areas: Other

Original sources

Trial registrationEvaluation of the NEUROSWING Orthosis on Walking Speed in a Population With Dorsal and/or Plantar Flexor Deficits, With a View to a Reimbursement Application ↗

Supporting passages (13)

study design"studyType": "INTERVENTIONAL"

sample size"count": 34, "type": "ESTIMATED"

randomized"allocation": "RANDOMIZED"

controlled"type": "ACTIVE_COMPARATOR"

regulatory approval"isFdaRegulatedDevice": false

research categories"primaryPurpose": "HEALTH_SERVICES_RESEARCH"

relevant ms types"Multiple Sclerosis",

intervention"name": "NEUROSWING Orthosis (experimental) : carbon orthosis with an active ankle articulation"

comparator"name": "Carbon orthosis (control)"

primary endpoint"measure": "Walking speed : 10m walk test"

follow up"timeFrame": "At all 12 visits from baseline (day 1), to end of study (day 35)"

findingsNo results are posted.

limitationsTrial registry record. Publication date: unknown. No results are posted. Planned enrolment and endpoints are not findings.

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