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Clinical Study of a Novel Rehabilitation Technique for Post-Stroke Hemiplegia Based on Motion Visual Capture and Electromyography Analysis in Traditional Chinese Medicine Practice.

Clinical Study of a Novel Rehabilitation Technique for Post-Stroke Hemiplegia Based on Motion Visual Capture and Electromyography Analysis in Traditional Chinese Medicine Practice.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080158
Enrollment
Unknown
Registered
2024-01-22
Start date
2024-02-01
Completion date
Unknown
Last updated
2024-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

stroke

Interventions

Tai Chi group:Intervention group: underwent modified 24 style Tai Chi exercise training (30 minutes) and conventional rehabilitation training (30 minutes), three times a week, for a total of 12 weeks.
control group:The control group received a routine rehabilitation plan, including active movement of limb muscles and joints, proprioceptive neuromuscular promotion, muscle resistance training, stretc
Experiment 1: Biomechanical Study of Tai Chi Subject:By using kinematic analysis methods such as 3D motion capture systems and surface electromyography instruments, the kinematic and dynamic parameter

Sponsors

Zhongda Hospital of Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Experiment 1: ? Have more than 1 year of experience in practicing Tai Chi; ? Good health condition, with no history of lower limb or joint injuries in the past 6 months; ? Agree to participate in this experiment and sign an informed consent form; ? Age range from 18 to 70 years old; Experiment 2: ? Computed tomography (CT) and/or MRI confirmed as a patient with cerebral infarction; ? First time, unilateral onset, or although there have been previous episodes but no residual neurological dysfunction; ? Stable vital signs; ? Age range from 18 to 70 years old; ? The course of the disease is 2-12 weeks; ? Unilateral paralysis, with lower limb muscle strength of level 3 or above on the affected side; ? The selected individual or their family members sign an informed consent form; ? The Modified Rankin Scale (MRS) score is = 3.

Exclusion criteria

Exclusion criteria: Experiment 1: ? Clinical imaging examination indicates knee osteoarthritis, knee joint fractures, dislocations, tuberculosis, tumors, infections, etc.; ? Individuals with a history of joint fractures, knee surgery, or other factors that may affect lower limb motor function; ? Individuals with obvious abnormalities in body structure (such as flat feet, high arched feet, X-shaped legs, etc.); ? Unable to cooperate with the evaluation and testing personnel for other reasons. Experiment 2: ? Having a history of epilepsy, having a history of idiopathic epilepsy among first-degree relatives, and using antiepileptic drugs; ? Serious cognitive and communication barriers that prevent cooperation in assessment and treatment; ? Posterior circulation cerebral infarction; Wearing a pacemaker and having metal implants in the skull; ? Severe cervical spondylosis, including severe cervical canal stenosis and cervical instability; ? Complete occlusion of the internal carotid artery; ? Skull defect; ? Pregnant women, etc.

Design outcomes

Primary

MeasureTime frame
Kinetic parameters of surface electromyography,eg.RMS, iEMG, aEMG;Kinematic parameters of dynamic visual capture,eg. COM, ROM;

Secondary

MeasureTime frame
Evaluation of ICF Core combination in Stroke;Modified Barthel Index(MBI);Fugl-Meyer assessment for upper extremity?(FMA-UE);

Countries

China

Contacts

Public ContactPei Wang

Zhongda Hospital of Southeast University

wangpei0717@126.com+86 159 5175 2352

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026