The Feasibility and Therapeutic Effect of Hybrid End-effector Robot-assisted Gait Training With an Active-assisted Module in Chronic Stroke Survivors

Not Applicable

Recruiting

• Conditions: Stroke; Rehabilitation; Robotic Rehabilitation

• Registration Number: NCT07034521
• Lead Sponsor: National Taiwan University Hospital

Brief Summary

Walking rehabilitation after stroke is most effective during the first three months of recovery, but even in the chronic phase-beyond six months post-stroke-a significant number of patients still show potential for gait improvement. Robot-assisted rehabilitation is becoming increasingly common in clinical settings, with various design modes available. However, the effectiveness of new products in improving gait or motor function still requires further investigation.

This study aims to evaluate the usability and therapeutic effects of a new end-effector exoskeleton robot system, HIWIN MRG-P110, for gait training in chronic stroke patients. The system uses foot pedal mechanisms to drive hip and knee movements for lower-limb training. Unlike its predecessor, this device allows adjustment of the active assistance ratio, encouraging users to engage in voluntary movement. It is designed for gait training in stroke patients and others with neurological impairments, but the usability and efficacy of this new training model remain to be verified.

This clinical trial is a randomized, single-blind, prospective study enrolling 60 stroke patients who are 6 months to 3 years post-onset and have a Functional Ambulation Category (FAC) level of 0 to 3. The study will explore how patients with varying degrees of motor weakness learn to adapt to the "active-assistive mode" in terms of speed and perception. Participants will be randomly assigned to either the active-assistive mode group or the fully passive mode group. Both groups will receive 15 treatment sessions over 5 weeks.

The study will compare the two groups in terms of:

1. Improvements in gait and balance immediately post-treatment and at 3-month follow-up

2. Changes in brain activity, as measured by functional near-infrared spectroscopy (fNIRS)

Detailed Description

Not available

Study Timeline

• Status Verified: 2025-06
• Study Start: 2025-06-01
• Study First Submitted: 2025-06-11
• Study First Submitted QC: 2025-06-19
• Last Update Submitted: 2025-06-19
• Study First Posted: 2025-06-24
• Last Update Posted: 2025-06-24
• Primary Completion: 2026-08
• Study Completion: 2026-12-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• Aged between 18 and 80 years old.
• First-ever stroke, confirmed by brain CT or MRI, with onset between 6 months and 3 years prior to enrollment.
• Walking ability classified as Functional Ambulation Category (FAC) level 0 (non-ambulatory) to level 3 (able to walk short distances indoors or outdoors only).
• Prior to the current stroke, the participant was an independent community ambulator without mobility impairments.

Exclusion Criteria

• Presence of lower limb joint contractures, deformities, or severe spasticity (Modified Ashworth Scale score of 4).
• Lower limb musculoskeletal conditions causing wounds, pain, inability to bear weight, or significant leg length discrepancy (>2 cm after orthotic correction).
• Known osteoporosis (T-score < -2.5) or history of osteoporotic fractures in the thoracolumbar spine or hip joints.
• Inability to use the exoskeleton device due to body size, including:

Body weight > 135 kg; Height < 145 cm or > 190 cm Thigh length < 38 cm or > 48 cm; Calf length < 48 cm or > 52 cm

• Cognitive or communication impairments that prevent understanding of study instructions or completion of questionnaires.
• Acute infections or unstable vital signs.
• Significant orthostatic hypotension or inability to maintain upright posture for more than 30 minutes.
• Use of indwelling urinary catheter, nasogastric tube, or tracheostomy.
• Pregnant women.
• Terminal illness with life expectancy less than six months.
• Inability to attend 15 rehabilitation sessions and follow-up assessment at 3 months.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
10 meter walk test	baseline, right after last session of intervension (within 1 week), 3 months after intervension

Trial Locations

Locations (1)

National Taiwan University Hospital; 🇨🇳 Taipei, Taiwan