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Clinical Trials/NCT05883059
NCT05883059
Recruiting
Not Applicable

Clinical Study On Lower Limb Robot For Lower Limb Dysfunction After Stroke

liuyong1 site in 1 country18 target enrollmentApril 1, 2023
ConditionsStroke

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Stroke
Sponsor
liuyong
Enrollment
18
Locations
1
Primary Endpoint
Change from Baseline Berg Balance Scale at 4 weeks
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The goal of this clinical trial is to learn about effect of lower robot in stroke population. The main question[s] it aims to answer are: the efficacy of lower limb robot assisted training in improving walking ability, lower limb function, cognition, and quality of life in stroke patients.The robot group of patients received lower limb robot assisted training combined with routine rehabilitation treatment. The control group only received routine rehabilitation treatment.Compare two groups to explore the therapeutic effect of lower limb robots on lower limb dysfunction after stroke.

Registry
clinicaltrials.gov
Start Date
April 1, 2023
End Date
May 1, 2024
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
liuyong
Responsible Party
Sponsor Investigator
Principal Investigator

liuyong

chief physcician

The First Affiliated Hospital of Dalian Medical University

Eligibility Criteria

Inclusion Criteria

  • In line with the diagnostic criteria for stroke in the Diagnostic Criteria for Various Cerebrovascular Diseases issued by the Chinese Medical Association in
  • First stroke or no residual dysfunction after previous stroke.
  • Participants have stable vital signs, clear consciousness, and no aphasia.
  • The onset time of stroke is between 2 weeks and 6 months after onset.
  • Age\>18 years old.
  • Presence of hemiplegic motor dysfunction.
  • Ability to walk with the help of a single person.
  • sign an informed consent form with the Participants or family member before treatment.

Exclusion Criteria

  • Participants have serious musculoskeletal or other mental nervous system disease.
  • Participants have contraindications to cardiovascular exercise.
  • Moderate to severe contracture of the patient's lower limbs (modified Ashworth scale, MAS\>2 for ankle, knee, or hip joints).
  • Presence of progressive or secondary brain injury leading to unstable condition.
  • Unilateral neglect or diseases that affect vision.
  • Participants have lower limb vein thrombosis.
  • Participants present with lower limb non healing ulcers and osteoporosis.

Outcomes

Primary Outcomes

Change from Baseline Berg Balance Scale at 4 weeks

Time Frame: baseline and 4 weeks

The Berg Balance Scale is a commonly used scale for evaluating balance ability in stroke Participants.Participants cooperate to complete the corresponding projects, and specialized assessors with professional knowledge in rehabilitation assessment will score based on the patient's completion status. The scale has a total of 14 items, including standing up from a sitting position, standing to sitting, standing independently, sitting independently, bed to wheelchair transfer, standing with eyes closed, standing with feet together, standing with upper limbs extended forward, standing with objects picked up from the ground, turning back to look, turning around for a week, alternating steps with both feet, standing with both feet in front of and behind, and standing with one leg. Each project has a maximum score of 4 and a ,minimum score of 0. The higher the score, the better the balance ability.

Change from Baseline functional ambulation category scale at 4 weeks

Time Frame: baseline and 4 weeks

The functional ambulation category scale is a commonly used scale for evaluating walking ability, with ratings ranging from 0 to 5. The higher the level, the better the walking ability.

Change from Baseline fugl-meyer assessment-lower extremity at 4 weeks

Time Frame: baseline and 4 weeks

The scale assesses the presence or absence of reflexes in the participants' lower limbs, as well as the presence of hyperreflexia, flexor coordination, extensor coordination, activities accompanied by coordination, activities without coordination, and speed.The higher the score, the better the lower limb motor ability

Secondary Outcomes

  • Change from Baseline modified barthel index at 4 weeks(baseline and 4 weeks)
  • Change from Baseline Gait parameters at 4 weeks(baseline and 4 weeks)
  • Change from Baseline Minimum Mental State Examination at 4 weeks(baseline and 4 weeks)

Study Sites (1)

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