Comparison of the Rehabilitation Effects on Upper Limb Function in Stroke Patients between Innovative Mirror Therapy and Traditional Mirror Therapy

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400079955

Enrollment

Unknown

Registered

2024-01-17

Start date

2023-01-01

Completion date

Unknown

Last updated

2024-01-22

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

Conditions

stroke

Interventions

Innovative Mirror Therapy Group: undergoes 20 minutes of conventional rehabilitation training before each session, followed by 20 minutes of innovative mirror motor therapy (MT) assisted by the Yi She

Traditional Mirror Therapy Group: undergoes 20 minutes of conventional rehabilitation training before each session, followed by 20 minutes of traditional mirror therapy with the assistance of a therap

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: ?The first onset was diagnosed as a unilateral cerebral hemisphere ischemia or hemorrhage, with a duration of 1-6 months. ?Accompanied by varying degrees of upper limb motor dysfunction caused by stroke. ?The modified Ashworth Scale (MAS) score for the affected finger flexor muscles is =2. ?There is no obvious pain or hand sensory impairment, the condition is stable, and rehabilitation treatment is tolerable. ?There is no severe depression or anxiety, normal cognitive function, and the ability to understand and follow treatment instructions. ?Good family support, good compliance, and willingness to cooperate in completing the trial.

Exclusion criteria

Exclusion criteria: ?Severe musculoskeletal disorders such as unstable upper limb fractures, joint deformities, finger deformities, etc. ?Not suitable for rehabilitation treatment due to serious infectious diseases, lung infections, urinary tract infections, etc. ?Patients with cognitive and functional limitations or complications that restrict their cognitive and functional abilities (such as mental disorders, orthostatic hypotension, deep vein thrombosis in the lower extremities, significant organ dysfunction, etc.) ?Pregnant women, breastfeeding women, or women of childbearing age planning pregnancy during the trial. ?Other conditions deemed unsuitable for inclusion by the researcher.

Design outcomes

Primary

Measure	Time frame
FMA-UE;FMA-WH;	—

Countries

China

Contacts

Public ContactTao Chen

First People’s Hospital of Shuangliu District, Chengdu City.

375197050@qq.com+86 136 8809 7547

Outcome results

None listed

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