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Clinical study on the improvement of hand function in stroke patients using rTMS combined with pneumatic glove training at different time intervals

Clinical study on the improvement of hand function in stroke patients using rTMS combined with pneumatic glove training at different time intervals

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094416
Enrollment
Unknown
Registered
2024-12-23
Start date
2024-12-23
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Stroke

Interventions

Pneumatic gloves rTMS timing group:Immediately perform rTMS treatment for 10 minutes after pneumatic glove treatment for 20 minutes
rTMS Pneumatic Glove Timing Group:After 20 minutes of rTMS treatment, immediately perform 10 minutes of pneumatic glove training
rTMS synchronous pneumatic glove group:Simultaneous treatment of rTMS and pneumatic gloves for 20 minutes

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria in the 'Diagnostic Guidelines for Major Cerebrovascular Diseases in China 2019' and is diagnosed with cerebral infarction or cerebral hemorrhage through head CT or MRI;(2) Age range: 18-80 years old;(3) First time, unilateral hemiplegic patients, 0.5 months = 20;(5) Brunstrom stage I-III of the affected upper limb and hand;(6) The patient is aware of and has signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Upper limb contractures, hemiplegic hands, or abnormally increased muscle tone in the upper limbs;(2) Individuals with a history of epilepsy, contraindications to the use of epileptic drugs or brain stimulation, wearing pacemakers, intracranial metal implants, etc. who are unable to receive transcranial magnetic therapy;(3) Individuals with skull defects, head infections, and skin damage who are unable to cooperate with near-infrared testing;(4) People with hand dysfunction caused by other reasons before the onset of the disease;(5) Patients with severe cardiovascular, pulmonary, and renal complications, as well as other neurological disorders.

Design outcomes

Primary

MeasureTime frame
FMA Upper Limb Motor Function Evaluation;

Secondary

MeasureTime frame
HbO2;functional test for the hemiplegic upper extremity, FTHUE-HK;Barthel index;

Countries

China

Contacts

Public ContactLong Jianjun

Shenzhen Second People's Hospital

longjianjun@szu.edu.cn+86 137 9835 7543

Outcome results

None listed

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