Actively Recruiting

Phase Not Applicable
Age: 65Years - 80Years
All Genders
ID06443008

Effect of Myoelectric Biofeedback Therapy Combined With Rehabilitation on Upper Limb Function in Elderly Patients With Cerebral Infarction

Led by The Fourth Affiliated Hospital of Zhejiang University School of Medicine · Updated on 2025-02-17

80

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effect of myoelectric biofeedback therapy on upper limb function in elderly patients who have had a cerebral infarction, commonly known as a stroke. The study aims to see if this therapy helps restore arm movement and to understand any medical issues related to the treatment. It compares the therapy combined with comprehensive rehabilitation to rehabilitation alone in patients aged 65 to 80 years. Participants are randomly assigned to one of two groups. The control group receives standard rehabilitation, including position adjustments, passive and active training, anti-spasm exercises, balance training, and activities to improve daily living skills. The observation group receives the same rehabilitation plus myoelectric biofeedback therapy, which involves attaching electrodes to specific muscles and using electrical stimulation at set frequencies. Patients perform tension and relaxation exercises guided by device signals for about 30 minutes daily, with increasing intensity over time. During the study, participants are evaluated on their upper limb function within three days of hospital admission, on the day of discharge, and one month after discharge. Researchers also assess quality of life related to stroke at these times. The study includes monitoring of therapy effects and patient compliance. Total participation spans from hospitalization through one month post-discharge, with ongoing assessments to measure recovery and the impact of the therapy.

CONDITIONS

Brief Title

Effects of Myoelectric Biofeedback on Upper Limb Function in Post-stroke Patients

Who Can Participate

Age: 65Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subject volunteered to participate and signed informed consent
  • Age 65 to 80 years old, any gender
  • Diagnosis of stroke
  • No other major cardiovascular diseases
Not Eligible

You will not qualify if you...

  • Poor compliance
  • Skin allergies
  • Not meeting diagnostic or inclusion criteria
  • Severe consciousness disorders, severe dementia, or speech disorders preventing communication
  • Unable to cooperate as required
  • Currently participating in other clinical trials

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - During hospitalization and up to 1 month after discharge

Participants receive comprehensive rehabilitation training. Those in the observation group also receive myoelectric biofeedback therapy, which involves attaching electrodes to specific muscles and performing guided muscle tension and relaxation exercises.

Visits within 3 days of hospitalization, on the day of discharge, and one month after discharge

Trial Site Locations

Total: 1 location

1

Yinkai Cheng

Yiwu, Zhejiang, China, 310000

Actively Recruiting

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Research Team

Y

Yinkai Cheng

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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