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Clinical study of intermittent Theta burst magnetic stimulation (TBS) in the treatment of upper limb dysfunction in stroke patients

Clinical study of intermittent Theta burst magnetic stimulation (TBS) in the treatment of upper limb dysfunction in stroke patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069227
Enrollment
Unknown
Registered
2023-03-10
Start date
2023-03-10
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Stroke

Interventions

Study 1: Stroke group:intermittent Theta burst magnetic stimulation (TBS)
Study 1: Healthy control group:intermittent Theta burst magnetic stimulation (TBS)
Study 2: Regular training group:Regular training
Study 2: Sham stimulation group:Routine training+iTBS in M1 area of the affected side+false stimulation of SMA on the affected side
Study 2: Experimental group:Routine training group+affected side M1 and SMA iTBS

Sponsors

Huashan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria of healthy people: (1) Aged 18-80 years and the gender is not limited; (2) Clear consciousness and stable vital signs; (3) Be aware of this research and voluntarily sign the informed consent. 2. Inclusion criteria of patients: (1) Meet the diagnostic criteria of stroke in the Fourth National Conference on Cerebrovascular Disease; (2) First subcortical stroke; (3) Hemiplegia, Brunnstrom grade upper limb and hand ?-?; (4) The Modified Ashworth Scale (MAS) was lower than grade 2; (5) Aged 18-80 years, and the course of disease was 6-12 months; (6) Clear consciousness and stable vital signs; (7) Know about this research and sign the informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1. Exclusion criteria for healthy people: (1) Diseases of the nervous system, bone and joint, and muscles that affect motor function; (2) Severe cardiopulmonary, liver and kidney dysfunction; (3) Epilepsy; (4) Severe cramps or pain; (5) Severe speech, attention, hearing, vision, sensory, intellectual, mental or cognitive impairment; (6) History of malignant tumor disease; (7) Patients with metal objects or magnetic plates in the skull, cardiac pacemakers, medical implant devices such as cardiac wires and central venous catheters; (8) Patients with malignant hypertension. 2. Exclusion criteria for patients: (1) Diseases of bone, joint and muscle; (2) Other serious neurological diseases; (3) Complicated with severe cardiopulmonary, liver and kidney dysfunction; (4) Epilepsy; (5) Severe spasms or pain; (6) Severe speech, attention, hearing, visual, sensory, intellectual, mental or cognitive impairment (MMSE>24/30); (7) History of malignant tumor disease; (8) Patients with metal objects or magnetic plates in the skull, cardiac pacemakers, medical implant devices such as cardiac wires and central venous catheters; (9) Patients with malignant hypertension.

Design outcomes

Primary

MeasureTime frame
Diffusion tensor imaging indicators;

Secondary

MeasureTime frame
Simplified Fugl-Meyer Assessment (FMA) Score;Action Research Arm Test Assessment Score;Wolf Motor Function Test Assessment Score;Barthel Index Assessment Score;Brunnstrom Rating Scale;fNIRS indicators;Indicators of cortical excitability;

Countries

China

Contacts

Public ContactWang Yuyuan

Huashan Hospital Affiliated to Fudan University

Wangyuyuan1220@163.com+86 138 1891 5325

Outcome results

None listed

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