postpartum low back pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Meets the criteria for postpartum low back pain; (2) Low back pain occurred between 42 days and 2 years after delivery; (3) Aged 20-45 years; (4) No skin problems such as localised skin breakdown; (5) Voluntarily participate and sign an informed consent form after a full explanation of the purpose and procedures of this clinical trial, as well as any risks and potential adverse effects of this trial procedure
Exclusion criteria
Exclusion criteria: Those with one of the following conditions could not be included in this trial: (1) Patients with lumbar spine congenital sarcoidosis, spinal stenosis, narrow plate fracture, fracture, osteoporosis and other bony diseases; (2) Those who participated in other experimental interventions for low back pain symptoms within 2 weeks; (3) Pregnancy status or during the experiment pregnancy and family planning; (4) Malignant tumour, cancer pain metastasis, gynecological, urological, surgical, organ lesions or tuberculosis caused by low back pain; and (5) Suffering from serious heart, lung, brain, blood system diseases and diabetic patients; (6) Those who are unable to complete the basic course of treatment, have poor compliance and cannot adhere to the treatment according to the guideline and have difficulties in follow-up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| pain level;mental health; | — |
Secondary
| Measure | Time frame |
|---|---|
| Lumbar function;walking ability;range of motion of the trunk;quality of life; | — |
Countries
China
Contacts
Guangdong Hospital of Traditional Chinese Medicine