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The efficacy of alternating treatment of rTMS combined with soft hand rehabilitation robot on the recovery of hand function in patients after stroke

The efficacy of alternating treatment of rTMS combined with soft hand rehabilitation robot on the recovery of hand function in patients after stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089583
Enrollment
Unknown
Registered
2024-09-11
Start date
2024-10-01
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Stroke patients

Interventions

Group A:Group A will receive 10 Hz high-frequency rTMS over the iM1 for 20 minutes, followed by 20 minutes of SRG, totaling 40 minutes. 1 time/day, 5 days/week
Group B:Group B will receive 5 minutes of 10 Hz high-frequency rTMS over iM1 followed by 5 minutes of SRG, repeated four times, totaling 40 minutes.1 time/day, 5 days/week
Group C:Group C will receive rTMS with the sham coil, with the same parameters as group A. All patients will receive routine rehabilitation training. In addition, patients will receive a 4-week neurol

Sponsors

The First Affiliated Hospital of Nanjing Medical University/Jiangsu Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) ischemic stroke confirmed by CT and/or MRI meets the diagnostic criteria for cerebral infarction in the cerebrovascular disease; (2) primary or unilateral onset or previous onset without residual neurological dysfunction; (3) stable vital signs and clear consciousness; (4) the age ranges from 40 to 70 years; (5) the course of disease ranges from 1 week to 3 months; (6) Brunnstrom of hemiplegic upper limb and hand staging from I to III; (7) without cognitive dysfunction; and (8) the selected candidate or their relatives sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) epilepsy in the previous, a family history of epilepsy and taking medications that cause seizures; (2) severe deficits in cognition and communication that impede patient participation during evaluation and therapy; (3) posterior circulation infarction; (4) wearing a pacemaker, intracranial metal implants; (5) severe cervical spondylosis includes severe cervical stenosis and cervical spinal instability; (6) complete occlusion of the internal carotid artery; (7) direct injuries and skull defects in the stimulation area; and (8) women during pregnancy.

Design outcomes

Primary

MeasureTime frame
Fugl-Meyer Assessment – Upper Extremity;

Secondary

MeasureTime frame
Functional Test for the Hemiplegic Upper Extremity;Modified Ashworth Scale;ICF-Upper Extremity Entries;

Countries

China

Contacts

Public ContactShen Ying

The First Affiliated Hospital of Nanjing Medical University/Jiangsu Provincial People's Hospital

shenying_1981@hotmail.com+86 139 1391 3930

Outcome results

None listed

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