Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT05908149

Gait Analysis in Patients With Hemiplegia Using Insole Splint.

Led by University of Ioannina · Updated on 2024-12-06

12

Participants Needed

1

Research Sites

142 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to compare the gait of patients with hemiplegia, with or without the use of insole splint. The main questions it aims to answer are: Does the insole splint improve the gait of these patients? Does any difference exist in the use of muscles? Participants will have to walk in the gait analysis' aisle with and without the insole splint, using wireless EMG device.

CONDITIONS

Official Title

Gait Analysis in Patients With Hemiplegia Using Insole Splint.

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Able to walk with or without the splint
  • First stroke episode at least two months ago
  • Hospitalization period no longer than six months
  • Diagnosis confirmed by neurologist with Brain CT-scan
  • Used insole splint during physiotherapy for at least one week
  • Able to communicate and understand instructions
  • Age between 18 and 70 years
  • Functional Ambulation Category (FAC) greater than 2
  • Modified Ashworth Scale (MAS) of affected lower limb 2 or less
  • Normal gait before the stroke
Not Eligible

You will not qualify if you...

  • Peripheral neurological damage
  • Past or ongoing orthopedic or rheumatologic disease affecting gait
  • Past damage of the central nervous system
  • Skin problems or other factors limiting use of insole splint
  • Recent intramuscular botox injection
  • Low motivation or poor perception

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Physical Medicine and Rehabilitation, University Hospital of Ioannina

Ioannina, Greece, 45100

Actively Recruiting

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Research Team

A

Avraam Ploumis

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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