None
Conditions
Interventions
Experimental group:On different test days, participants received four types of stimulation: 1Hz rTMS, 10Hz rTMS, iTBS, and cTBS, but only one type each time. All stimulations were applied to the M1 ha
Sponsors
The First Affiliated Hospital of Air Force Military Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Aged between 18 and 45, any gender. 2. In good health, with no history of serious heart, lung, neurological, or mental illnesses. 3. No TMS contraindications, such as intracranial metal implants, history of seizures, or serious head trauma. 4. Willing to participate in this study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. People who have had rehabilitation treatment or surgery related to the diaphragm in the past month. 2. People who have participated in other clinical trials in the past month that could affect the study results. 3. People with communication problems, severe hearing or vision impairments, or cognitive dysfunction who can't complete the assessments. 4. People with a history of drug or alcohol abuse, or who have recently used drugs that could affect central nervous system excitability and TMS effects, including but not limited to benzodiazepine sedatives, anticonvulsants, antipsychotics, etc. 5. Women who are pregnant or breastfeeding.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Diaphragm motor evoked potential; | — |
Secondary
| Measure | Time frame |
|---|---|
| Resting pulmonary function parameters; | — |
Countries
China
Contacts
Public ContactHua Yuan
The First Affiliated Hospital of Air Force Military Medical University
Outcome results
None listed