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A randomized controlled clinical study on the effect of mirror visual feedback therapy combined with acupuncture on upper limb function reconstruction after stroke

Clinical study of mirror vision feedback therapy combined with acupuncture on upper limb function reconstruction after stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077010
Enrollment
Unknown
Registered
2023-10-26
Start date
2022-01-01
Completion date
Unknown
Last updated
2023-10-30

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

Conditions

Upper limb dysfunction after stroke

Interventions

MVF group:Routine upper limb rehabilitation training+ MVF training
Acupuncture treatment group:Routine upper limb rehabilitation training+ Acupuncture therapy
MVF combined with acupuncture treatment group:Routine upper limb rehabilitation training+ MVF training+ Acupuncture therapy

Sponsors

Shibei Hospital of Jing'an District, Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
43 Years to 78 Years

Inclusion criteria

Inclusion criteria: ? The patient was diagnosed as the first onset within 6 months, stable and conscious, accompanied by upper limb dysfunction; ? Age 30-80 years old; (3) Sign informed consent; Can cooperate to complete training and evaluation, compliance is good; ? right-handed; (5) Education level above primary school; ? eliminate the upper limb dysfunction caused by skeletal muscle disease; ? Brunnstrom Grade II-IV for distal upper limb joints; ? No cognitive dysfunction, the score of mini-mental state examination (MMSE) > 17.

Exclusion criteria

Exclusion criteria: ? Suffering from severe hypertension or cardiopulmonary disease; ? Severe joint pain; ? Patients with severe impairment of vision, hearing and comprehension; ? deformity of upper limbs and hands. (5) Bilateral brain lesions, bilateral limb function disorders, lesions located in the cerebellum or brain stem; ? Progressive stroke or subarachnoid hemorrhage; ? Severe cognitive impairment, depression or severe aphasia after stroke; ? craniocerebral trauma or tumor; ? Patients or their families do not cooperate and do not sign informed consent.

Design outcomes

Primary

MeasureTime frame
Functional magnetic resonance;

Secondary

MeasureTime frame
Fugl-Meyer Assessment-Upper Extremities;Modified Barthel Index;Action Research Arm Test;

Countries

China

Contacts

Public ContactJIN SHU

Shibei Hospital of Jing'an District, Shanghai

shu_jin@126.com+86 189 1825 5966

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026