Actively Recruiting
Effects on Subacute Stroke With Robotic Assistive Gait Training
Led by Changhua Christian Hospital · Updated on 2025-06-27
40
Participants Needed
1
Research Sites
43 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this randomized controlled trial is to learn about the effects of Robotic Assisted Gait Training (RAGT) combined with traditional physical therapy in subacute stroke patients. The main question it aims to answer is: \- Does RAGT combined with traditional physical therapy improve gait and functional performance in subacute stroke patients compared to traditional physical therapy alone? Participants who are subacute stroke patients will be randomly assigned to receive either both RAGT and traditional physical therapy or only traditional physical therapy. Their gait and functional performance will be assessed during the study period.
CONDITIONS
Official Title
Effects on Subacute Stroke With Robotic Assistive Gait Training
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with stroke (ischemic or hemorrhagic) confirmed by medical imaging.
- Stroke onset within 1 to 3 months (subacute phase).
- Moderate to good standing balance ability.
- Sufficient cognitive ability to understand the study and follow instructions.
- Able to participate in rehabilitation training during the study period.
- Age between 45 and 70 years.
You will not qualify if you...
- Body weight over 90 kg.
- Presence of other neurological disorders.
- Severe cardiovascular disease or other health conditions affecting mobility.
- Significant lower limb pain, joint contracture, or spasticity (Modified Ashworth Scale score > 3) that impairs walking.
- Diagnosed with cardiopulmonary disease that contraindicates exercise training.
- Cognitive impairment that prevents understanding of training instructions or completion of questionnaires.
- Inability to complete the rehabilitation training protocol.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Changhua Christian Hospital
Changhua, Taiwan, Taiwan, 500
Actively Recruiting
Research Team
O
Office of Human Subject Protection Changhua Christian Hospital
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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