Postpartum Anxiety
Conditions
Interventions
Experimental Group:Interventional Device: Transcranial photobiomodulation device
Core Parameters: Irradiation wavelength: 1064 nm
Output power: 250 mW
Irradiation Site: Parietal lobe, bilateral prefrontal lobes
Intervention Duration and Frequency
Single irradiation duration: 20 minutes per session
Intervention time points: On th
the implementation of each intervention shall be recorded.
Control Group:Same device and operation as the intervention group, no effective irradiation.
Sponsors
Yan'an City Hospital of TCM
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1. Age 18–45 years old; 2. Full-term pregnancy (>=37 weeks), planning to give birth in this hospital and complete post-partum hospitalization observation; 3. Able to understand the research process and sign the informed consent form; 4. Acceptable to have equipment contact and irradiation on the forehead (no obvious skin contraindications).
Exclusion criteria
Exclusion criteria: 1.The parturient or their family members refuse. 2. Complicated with oral ulcers, bleeding, or inflammation. 3. Complicated with diabetes or thyroid disease. 4. A clear history of past or current mental disorders, bipolar disorder, or at risk of acute suicide. 5. A clear history of major neurological diseases (such as a history of epileptic seizures, etc.) or a history of photosensitivity-related diseases. 6. Frontal skin damage, infection, severe dermatitis, or areas unsuitable for contact after surgery. 7. Severe postpartum complications requiring ICU/emergency treatment, making it impossible to complete the research process.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Incidence rate of anxiety; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence rate of depression;Salivary metabolomics;Sleep quality;Pain score; | — |
Countries
China
Contacts
Public ContactZhao Huiling
Yan'an City Hospital of TCM
Outcome results
None listed