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Clinical study on the treatment of upper limb dysfunction in stroke patients using eye acupuncture combined with mirror therapy

Clinical study on the treatment of upper limb dysfunction in stroke patients using eye acupuncture combined with mirror therapy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000865
Enrollment
Unknown
Registered
2024-12-25
Start date
2024-12-27
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Stroke

Interventions

Regular Group:Upper limb rehabilitation training
Eye needle group:Eye acupuncture combined with mirror imaging and upper limb training
Mirror Group:Mirror therapy combined with upper limb rehabilitation training

Sponsors

Huludao Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Confirmed by head CT or MRI the imaging findings are consistent with cerebral infarction or cerebral hemorrhage. 2) First onset with a course of less than 3 months. 3) Age between 35-75. 4) Brunstrom stage of the affected upper limb is stage III or above. 5) Muscle tone of the affected upper limb is not higher than stage II (Modified Ashworth Scale MAS). 6) Vital signs are stable without severe cognitive or comprehension dysfunction. The Loewenstein Occupational Therapy Cognitive Assessment (LOTCA) score should not be less than 40 points. 7) There should be no serious heart liver kidney or other organ diseases. 8) Family members should give informed consent and be approved by the hospital ethics committee.

Exclusion criteria

Exclusion criteria: 1) Pain caused by various reasons can affect the movement of various joints in the upper limbs. For example shoulder hand syndrome elbow joint contracture etc. 2) accompanied by other serious diseases cannot complete this experiment. For example patients with circulatory and respiratory system related diseases as well as those with coagulation dysfunction or severe bleeding tendency. Patients with severe cognitive impairment and those who have previously suffered from psychiatric disorders. Patients who have undergone clinical trials of other drugs in the previous month before enrollment

Design outcomes

Primary

MeasureTime frame
Fugl Meyer Upper Limb Motor Function Scale;

Secondary

MeasureTime frame
modified Barthel index;Improved Ashworth assessment;

Countries

China

Contacts

Public ContactLiu jiye

Huludao Central Hospital

17704286805@163.com17704286805

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026