A study on the impact of visual motor imagery on upper limb function in stroke patients based on near-infrared brain functional imaging technology

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400081810

Enrollment

Unknown

Registered

2024-03-13

Start date

2022-01-08

Completion date

Unknown

Last updated

2024-03-18

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

Conditions

stroke

Interventions

Control group:Control group treatment: only receiving routine rehabilitation treatment

experimental group:Treatment in the experimental group: visual motor imagination combined with routine rehabilitation therapy

Eligibility

Sex/Gender

All

Age

21 Years to 80 Years

Inclusion criteria

Inclusion criteria: All stroke patients meet the diagnostic criteria of the "2018 China Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke" and the "2019 China Guidelines for the Diagnosis and Treatment of Cerebral Hemorrhage" revised and formulated by the Neurology Branch of the Chinese Medical Association and the Cerebrovascular Disease Group. (1) Age range from 21 to 80 years old; (2) First onset, unilateral lesion; (3) The course of the disease is less than 6 months; (4) Brunnstrom staging of the affected upper limb in stages I-III; (5) Minimum mental state examination (MMSE) score = 27 points, can cooperate with rehabilitation training; (6) The Kinesthetic and Visual Imagery Questionnaire (KVIQ) scores = 25; (7) International standard visual acuity chart examination, binocular vision or corrected vision = 1.0; (8) The patient or their family members sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Having a history of epilepsy, or having a history of idiopathic epilepsy among first-degree relatives, or having used antiepileptic drugs; (2) Impairment or failure of important organs such as the heart, lungs, liver, and kidneys; (3) Serious cognitive and communication barriers that prevent cooperation; (4) Severe audiovisual impairment or unilateral neglect.

Design outcomes

Primary

Measure	Time frame
Fugl-Meyer Assessment-Upper Extremity, FMA-UE);Average value of Oxy-Hb concentration changes detected by fNIRs;	—

Secondary

Measure	Time frame
modified barthel index;	—

Countries

Chian

Contacts

Public ContactJialing Wang

Zhejiang Rehabilitation Medical Center

736611363@qq.com+86 152 0503 1859

Outcome results

None listed

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