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Study on the effect of pelvic and abdominal mechanical exercise on rapid recovery after cesarean section

Study on the effect of pelvic and abdominal mechanical exercise on rapid recovery after cesarean section

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092522
Enrollment
Unknown
Registered
2024-11-18
Start date
2024-08-08
Completion date
Unknown
Last updated
2024-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastrointestinal function recovery and pelvic floor dysfunction after cesarean section

Interventions

Experimental group:Pelvic abdominal mechanical movement+Routine cesarean section postoperative and puerperium management
Control Group:Routine cesarean section postoperative and puerperium management

Sponsors

Shanghai Tongren Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Full-term pregnancy (37 weeks to 42 weeks of gestation), aged 18-45 years for elective cesarean section; 2. Transabdominal lower uterine segment cesarean section, anesthesia with combined spinal-epidural anesthesia; 3. Subjects who agree to sign the informed consent form and have not participated in other clinical trials of therapies or drugs.

Exclusion criteria

Exclusion criteria: 1. Patients who underwent cesarean section due to abnormal fetal position, abnormal labor process, fetal distress and other reasons; 2. Patients with chronic digestive system diseases that affect gastrointestinal motility such as chronic constipation, irritable bowel syndrome, ulcerative colitis and other chronic digestive system diseases before surgery; 3. Patients with serious internal and external diseases such as cardiovascular, endocrine, blood, immune, and urinary systems; 4. Patients with severe pelvic adhesions found during surgery; 5. Patients who used drugs that affect gastrointestinal motility after surgery, such as mosapride tablets; 6. Patients with severe lower back pain, spinal deformity, lumbar disc herniation, postoperative exercise contraindications, and difficulty in completing pelvic and abdominal mechanical exercise guidance movements; 7. Patients with mental illness and consciousness disorders who cannot cooperate; 8. Patients who do not agree to receive treatment in the treatment group or control group and have not signed informed consent.

Design outcomes

Primary

MeasureTime frame
Time of first anal gas discharge;

Secondary

MeasureTime frame
Time of first anal defecation;Incidence of adverse reactions of digestive system;Pain score;Emotional state during postpartum;Pelvic floor muscle recovery;General self-efficacy; Quality of Life Questionnaire;

Countries

China

Contacts

Public ContactQiu Jin

Shanghai Tongren Hospital

jeanqiugiu@hotmail.com+86 181 2122 6319

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026