By InvitationNot Applicable

Tracking Self-Reported Functional Needs and Quality of Life

United States1,000 participantsStarted 2025-11-26

Plain-language summary

The study aims to characterize the population of Cionic Neural Sleeve users and assess their health-related quality of life.

Who can participate

Age range22 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Resident of the United States * New customer awaiting the Cionic Neural Sleeve Exclusion Criteria: * Implanted demand-type cardiac pacemaker or defibrillator * Malignant tumor or existing thrombosis in the impacted or more impacted leg * Fracture or dislocation in the impacted or more impacted leg that could be adversely affected by motion from stimulation

What they're measuring

Health Related Quality of Life

Timeframe: Day 0, Month 1, Month 2, Month 3, Month 6, Month 9, Month 12

Trial details

NCT IDNCT07284810

SponsorCionic, Inc.

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2027-03

View on ClinicalTrials.gov More Upper Motor Neuron Disease trials