Pelvic pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.>=18 years old; 2. Women after 42 days postpartum; 3. Voluntarily participate in this study and sign the informed consent form. If the subject does not have the ability to read the informed consent form (e.g., illiterate subjects), the witness must witness the informed consent process and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Open scalp lesions or severe dermatitis or other conditions where electrode placement may aggravate skin problems and cause infection. 2. Acute brain diseases (such as cerebral hemorrhage, cerebral edema, intracranial infection, or uncontrolled seizures, etc.). 3. History of metal implants or foreign bodies in the body (incompatible implants), photosensitive diseases, or photoallergy. 4. Vulnerable groups other than illiterate, including people with mental illness, cognitive impairment, critically ill patients, pregnant women, etc.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Functional Magnetic Resonance Imaging;Electroencephalogram;Functional Near-Infrared Spectroscopy; | — |
Secondary
| Measure | Time frame |
|---|---|
| McGill Pain Questionnaire;Hamilton Anxiety Scale score;Hamilton Depression Rating Scale score;Visual Analog Scale; | — |
Countries
China
Contacts
Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University