Actively Recruiting

Phase Not Applicable
Age: 40Years - 80Years
All Genders
NCT06897631

Robot-Assisted Tai Chi for Upper Limb Rehabilitation in Stroke Patients

Led by Jing Tao · Updated on 2026-01-28

120

Participants Needed

2

Research Sites

87 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study aims to compare the effectiveness of Robot-Assisted Tai Chi Training (RATT) versus conventional rehabilitation in improving upper limb motor function post-stroke, and to explore the neuromuscular mechanisms of RATT. Participants will be randomly assigned to one of two groups: 1. Robot-Assisted Tai Chi Training group: Participants will receive guided Tai Chi arm movements with robotic assistance to enhance coordination and strength. 2. Conventional rehabilitation group: Participants will perform standard exercises (e.g., stretching, repetitive task practice). Both groups will receive 60-minute sessions, administered 5 days a week, over 4 weeks. Researchers will measure improvements using clinical scales (e.g., Fugl-Meyer Assessment) and monitor safety.

CONDITIONS

Official Title

Robot-Assisted Tai Chi for Upper Limb Rehabilitation in Stroke Patients

Who Can Participate

Age: 40Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with stroke confirmed by neuroimaging (CT/MRI)
  • Fugl-Meyer Assessment for Upper Extremity score of 8-44
  • First-ever stroke with unilateral hemiplegia and time since onset �3 12 months
  • Aged 40-80 years, any gender
  • Voluntarily participated and provided written informed consent
Not Eligible

You will not qualify if you...

  • Severe cognitive impairment (Montreal Cognitive Assessment score <10)
  • Poor sitting balance (less than Grade 2) or unable to remain seated for over 60 minutes
  • Hypertonia (modified Ashworth Scale score >2 in affected limb)
  • Significant hemiplegic shoulder pain (Visual Analogue Scale >3)
  • Severe aphasia (Boston Diagnostic Aphasia Examination score <3)
  • Severe visual impairment preventing robot-assisted upper limb training
  • Moderate-to-severe depression (Hamilton Depression Rating Scale score >17)
  • Pre-existing neuromuscular disorders, active cancers, or uncontrolled heart, kidney, or liver diseases
  • Participating in other clinical trials that could affect this study's results

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Rehabilitation Hospital Affiliated to Fujian University of Traditional Chinese Medicine

Fuzhou, Fujian, China, 350003

Actively Recruiting

2

The Third People's Hospital Affiliated to Fujian University of Traditional Chinese Medicine

Fuzhou, Fujian, China, 350122

Actively Recruiting

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Research Team

J

Jingsong Wu

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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