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Application of Transcranial Ultrasound in Rehabilitation of Upper Limb Function in Stroke Patients: A Clinical Observation Test

Application of Transcranial Ultrasound in Rehabilitation of Upper Limb Function in Stroke Patients: A Clinical Observation Test

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900026683
Enrollment
Unknown
Registered
2019-10-18
Start date
2019-10-17
Completion date
Unknown
Last updated
2019-10-28

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

Conditions

Ischemic stroke

Interventions

Group A:0.5 W/cm2 TUS
Group B:0.75 W/cm2 TUS
Group C:sham TUS(Non-working mode)

Sponsors

The Second Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. First ever subacute ischemic stroke, conformed to the "guidelines for diagnosis and treatment of acute ischemic stroke in China 2014" and confirmed by CT or MRI imaging scan; 2. 1 months after the stroke event; 3. Aged 18-85 years; 4. Residual upper limb impairment; 5. Brunnstrom motor recovery stages (BMRS) of the affected side upper limb and hand at least stage III; 6. Conscious, vital signs stable and ability to cooperate with training; 7. Commit to follow the research procedures and cooperate with the implementation of the whole research process; 8. Commit to following lifestyle tips during the research 9. Willing to sign the informed consent for this study.

Exclusion criteria

Exclusion criteria: 1. Consciousness disorder, cognitive dysfunction, mental disorder or mixed aphasia; 2. Hemorrhagic cerebral infarction; 3. Intractable epilepsy; 4. With serious dysfunction of liver, kidney, heart and other important organs; 5. Severe shoulder pain or severe limitation of range of motion in shoulder and elbow joints; 6. With musculoskeletal disorders that affect upper limb movement disorders; 7. Internal cardiac pacemaker or intracranial implantation of other metal medical devices; 8. Severe impairment of vision or hearing; 9. Woman who is pregnant or nursing; 10. The absence of a skull; 11. The investigator considers that there are any conditions that could harm the subject or cause the subject to fail to meet or perform the study.

Design outcomes

Primary

MeasureTime frame
the Wolf Motor Function Test;Jebsen Hand Function Test, JHFT;

Secondary

MeasureTime frame
the Upper Extremity Section of the Fugl-Meyer Assessment, FMA-UE;Motion Evoked Potential;resting motor threshold;active motor threshold;cortex silent period;mini-mentalstateexamination;Montreal cognitive assessment;event-related potential;

Countries

China

Contacts

Public ContactZhang qiaojun

The Second Affiliated Hospital of Xi'an Jiaotong University

zhangqj@xjtu.edu.cn+86 13891867155

Outcome results

None listed

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