Diastasis Recti Abdominis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Women aged 20-40 years, 6 weeks to 1 year after a singleton, full-term delivery (vaginal delivery or cesarean section); (2) Diagnosed with diastasis recti abdominis by high-frequency ultrasound: inter-rectus distance (IRD) = 2.0 cm at least at one of the three measured points (umbilicus, 3 cm above umbilicus, 3 cm below umbilicus); (3) Voluntarily participate in this study and sign a written informed consent form.
Exclusion criteria
Exclusion criteria: (1) Presence of abdominal wall hernia, history of abdominal surgery (excluding cesarean section), or severe abdominal organ diseases; (2) Combined with severe cardiovascular, cerebrovascular, liver, kidney, or hematopoietic system diseases, or mental disorders; (3) Facial skin infection, damage, or severe allergies; (4) Currently participating in other interventional clinical trials that may affect the results of this study; (5) Severe fear of or intolerance to acupuncture.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in Inter-Rectus Distance (IRD); | — |
Secondary
| Measure | Time frame |
|---|---|
| Absolute Inter-Rectus Distance (IRD);Clinical cure rate;Core Muscle Strength;Low Back Pain Intensity;Quality of Life;Self-assessment of abdominal morphology and function; | — |
Countries
China
Contacts
Yantai Yuhuangding Hospital