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Investigation of effect of high and low frequency rTMS on hand function recovery in stroke patients

Investigation of effect of high and low frequency rTMS on hand function recovery in stroke patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023555
Enrollment
Unknown
Registered
2019-06-02
Start date
2019-06-17
Completion date
Unknown
Last updated
2019-06-03

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

Conditions

stroke

Interventions

Low frequency rTMS group:1 Hz rTMS stimulation+rehabilitation therapy
High frequency rTMS group:10 Hz rTMS stimulation+rehabilitation therapy

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Voluntary signing of informed consent and willingness to participate in this study; 2. Aged 20 to 75 years, male or female; 3. According to the "Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke in China" (1995 edition), diagnosed as cerebral infarction; diagnosed as cerebral hemorrhage according to "Guidelines for the diagnosis and treatment of Chinese cerebral hemorrhage" (1995 edition); 3. Comply with the CRPS diagnostic criteria proposed by the IASP (Budapest standard); 4. Confirmed by CT or MRI; 5. MMSE Score meets the following criterria: 17 for those who never received education, 20 for those went to elementary school(less than 6 years), 20 for those who went to secondary school(more than 6 years); 6. Hand function impairment for paretic side, Brunnstrom level less than III, disease duration less than 12 months; 7.The vital signs are stable, without serious speech and cognitive impairments, which can be easily communicated and can be combined with rehabilitation therapy.

Exclusion criteria

Exclusion criteria: 1. Unable to complete motor imagery confirmed by motor and visual questionnaires; 2. Obvious cognition impairment; 3. Contraindications for MRI due to metal implants in body; 4. History of seizure; 5. Pregnant or feeding; 6. Severe cardiovascular, respiratory, liver and kidney diseases, unstable clinical symptoms; 7. Poor compliant and failed to complete the whole study; 8. Participating in other relevant clinical researchers at the same time.

Design outcomes

Primary

MeasureTime frame
motor function;

Secondary

MeasureTime frame
ADL;MEP;Nerve conduction velocity;

Countries

China

Contacts

Public ContactGao Tianhao

Huashan Hospital, Fudan University

641202745@qq.com+86 15601720816, +86 18121186606

Outcome results

None listed

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