Effects of Tai Chi Yunshou motor imagery training for hemiplagic upper extremity motor function in patients with stroke

Effects of contralateral Tai Chi Yunshou motor imagery training and contralateral motor imagery training for hemiplagic upper extremity motor function in patients with stroke

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ITMCTR

Registry ID

ITMCTR2200006622

Enrollment

Unknown

Registered

2022-09-19

Start date

2022-09-06

Completion date

Unknown

Last updated

2023-02-20

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

Conditions

Stroke

Interventions

control group:contralateral motor imagery training and routine rehabilitation training

test group:contralateral Taiji Yunshou motor imagery training and routine rehabilitation training

Eligibility

Sex/Gender

All

Age

40 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) First stroke and in accordance with the "Diagnostic Essentials of Various Major Cerebrovascular Diseases in China 2019", confirmed by CT or MRI as cerebral infarction or cerebral hemorrhage. (2) Any gender, 40 years old = age = 80 years old. (3) Time of onset 2 weeks - 6 months (stroke recovery). (4) Edinburgh Handedness Inventory (EHI) test for right handedness. (5) Presence of hemiplegic upper extremity and hand with Brunnstrom's hemiplegic functional rating of II-V. (6) Kinesthetic and visual imagery questionnaire (KVIQ-20) score = 25, with motor imagery ability. (7) Ability to cooperate with motor imagery training. (8) The subject or his/her legal guardian (if necessary) understands, voluntarily participates in this research trial, and signs the Informed Consent Form.

Exclusion criteria

Exclusion criteria: (1) Serious speech, attention, hearing, vision, intelligence, spirit or cognitive impairment (MMSE = 26 points); (2) Complicated with serious primary or secondary diseases, such as serious liver and kidney hematopoietic system diseases, severe cardiopulmonary insufficiency, arrhythmia, etc; (3) Patients who are participating in other clinical trial studies; (4) Unable to cooperate with the complete training and assessment for any reason.

Design outcomes

Primary

Measure	Time frame
Fugl-Meyer Assessment of Upper Extremity, FMA-UE;	—

Secondary

Measure	Time frame
pinch;Modified Ashworth Scale, MAS;grip;Brunnstrom rating scale;Functional Test of the Hemiparetic Upper Extremity-Hong Kong,FTHUE-HK;Modified Barthel Index, MBI;	—

Countries

China

Contacts

Public ContactQiRui

qirui@shyueyanghospital.com18930566807

Outcome results

None listed

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