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Mobility Training Using a Bionic Knee Orthosis in Patients Chronic Post-Stroke: A Case Series

T

Tibion Bionics

Status and phase

Completed
Phase 4

Conditions

Stroke

Treatments

Device: Tibion Bionic Leg

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT01499862
CP 0003

Details and patient eligibility

About

This pilot study examined the effect of task-oriented mobility training in three persons chronic post-stroke using a novel, wearable, mobile intention-based robotic orthosis (Tibion Bionic Leg).

Enrollment

3 patients

Sex

All

Ages

40 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or female
  • Aged 40 to 60 years
  • One year status post-stroke
  • Able to walk at least 10 meters
  • Independence in self-care

Exclusion criteria

  • Medically unstable
  • Major cardiopulmonary deficiency
  • Major depression
  • Significant cognitive deficit
  • Currently receiving gait training
  • Younger than 40 years of age
  • Older than 60 years of age
  • Unable to walk at least 10 meters

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

3 participants in 1 patient group

Tibion Arm
Experimental group
Description:
Arm of the study in which enrolled post-stroke subjects undergo rehabilitative therapy with the Tibion Bionic Leg.
Treatment:
Device: Tibion Bionic Leg

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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