Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT06564090

Effect on Gait Pattern During Robot Assisted Gait Training (RAGT) of End-effector Type in Burn Patients

Led by Hangang Sacred Heart Hospital · Updated on 2024-08-21

60

Participants Needed

1

Research Sites

71 weeks

Total Duration

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AI-Summary

What this Trial Is About

This study aimed to investigate gait pattern and muscles power improvement of patient with gait disturbance caused by burns after end-effector type robot (Morning Walk®)-assited gait training (RAGT). This study randomly assigned 36 patients to one of two group : 30 minutes of Morning Walk® training with 30 minutes conventional physiotherapy (RAGT group) or 60 minutes of conventional physiotherapy (CON group). Five training sessions per week were given for 8 weeks. The primary outcomes were gait performance and muscles powers, which were assessed by the functional ambulation category (FAC) and the manual muscles test (MMT), respectively. The secondary outcomes included 6-minute walking test (6MWT), gait kinematic and spatiotemporal gait parameters. The results of this study is anticipated that the patients with gait disturbance receiving the RAGT might improve greater in gait performance and normal gait patterns that those trained with conventional physiotherapy.

CONDITIONS

Official Title

Effect on Gait Pattern During Robot Assisted Gait Training (RAGT) of End-effector Type in Burn Patients

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients who underwent split thickness skin graft at Hangang Sacred Heart Hospital
  • Burns involving more than 50% of the lower limb surface area
  • Age over 18 years
  • Functional ambulation category score of 3 or less
Not Eligible

You will not qualify if you...

  • Fourth-degree burns involving muscles, tendons, or bones
  • Severe communication disorders or psychological problems
  • Body weight over 135 kg or height over 195 cm
  • Physical conditions limiting therapy such as severe limb deformity, open wounds, pressure ulcers, or severe osteoporosis

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hangang sacred heart hodpital

Seoul, South Korea, 07247

Actively Recruiting

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Research Team

S

Sung Rakyum

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

2

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