Efficacy analysis and mechanism study of mirror therapy based on fNIRS on upper limb function recovery in stroke patients

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2200055439

Enrollment

Unknown

Registered

2022-01-09

Start date

2022-02-07

Completion date

Unknown

Last updated

2023-01-30

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

Conditions

Stroke

Interventions

Control group:Occupational therapy

Experimental group:Mirror therapy and occupational therapy

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Initial onset; patients with ischemic or hemorrhagic stroke confirmed by MRI or CT, all in line with the diagnostic criteria formulated by the Fourth National Cerebrovascular Disease Conference; 2. Movement disorder of upper limb and hand function on the hemiplegic side; 3. The first onset, the vital signs are stable, and the course of the disease is between 1 and 6 months; 4. Aged 18 to 75 years; 5. Upper limb function Brunnstorm stage 1-4; 6. The kinesthetic and imagery questionnaire (KVIQ) test was normal; 7. The mental rotation experiment is normal; 8. Clear consciousness, no serious cognitive impairment, no hearing or visual impairment; 9. Enough to sit independently or lean on for more than 30 minutes; 10. Informed consent to this study and signed the informed consent form and other relevant documents.

Exclusion criteria

Exclusion criteria: 1. Suffering from aphasia, apraxia, and lateral neglect; 2. Cognitive dysfunction: Mini-mental state examination (MMSE) score 3; 4. Accompanied by severe bone, joint and muscle disease or deformity; severe pain in the shoulder joint; severe passive joint range of motion of the shoulder and elbow joints is limited; 5. Previously suffering from other brain diseases or a history of brain surgery; 6. Upper limb dysfunction caused by other reasons; 7. Unstable disease or failure of vital organs, malignant tumor; 8. Unable to cooperate in completing the fNIRS inspection, etc.; 9. Pregnancy.

Design outcomes

Primary

Measure	Time frame
Assessment of near-infrared brain function;Fugl-Meyer upper limb motor function evaluation;Wolf motor function test;Arm action survey test form (ARAT);	—

Secondary

Measure	Time frame
Modified Ashworth for muscle tone assessment;Muscle strength;Visual analogue scale;Modified Barthel index;	—

Countries

China

Contacts

Public ContactYang Quan; Wang Jing; Liu Huiyu

Yuebei People's Hospital

569566514@qq.com+86 13600219290

Outcome results

None listed

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