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Tracking Self-Reported Functional Needs and Quality of Life

NCT07284810 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1000

Last updated 2025-12-17

No results posted yet for this study

Summary

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

Conditions

  • Upper Motor Neuron Disease

Interventions

DEVICE

Cionic Neural Sleeve System

The sleeve assists participants during physical activity by delivering electrical stimulation that helps contract the necessary muscles at the correct time to improve movement.

Sponsors & Collaborators

  • Cionic, Inc.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-26
Primary Completion
2027-03-31
Completion
2027-03-31
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07284810 on ClinicalTrials.gov