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Clinical research on the analysis of risk and protective factors for postpartum pelvic floor dysfunction diseases, establishment of predictive models, application, and evaluation of treatment strategies.

Clinical Study on the Establishment, Application, and Evaluation of Treatment Strategies for Predictive Models of Postpartum Pelvic Floor Dysfunction Diseases

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099112
Enrollment
Unknown
Registered
2025-03-18
Start date
2024-11-04
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

Postpartum pelvic floor disorders

Interventions

Pilot study:no
Modeling Group:no
Exercise Intervention Group:This study evaluates the effectiveness of Kegel exercises combined with WAFF pelvic floor exercises during late pregnancy and early postpartum in preventing pelvic floor di
Electrical Stimulation Group:Electrical stimulation for 20 minutes followed by biofeedback for 10 minutes. The patient should lie supine with hips and knees flexed after defecation and urination. The
Magnetoelectric Combined Group:In addition to the treatment protocol of the electrical stimulation group, magnetic therapy is added. Electrical stimulation for 20 minutes followed by biofeedback for 1
Radiofrequency and Electrical Combined Group:While completing the electrical stimulation protocol (20 minutes of electrical stimulation + 10 minutes of biofeedback, twice weekly for 5 weeks, totaling

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Gestational age at delivery >= 32 weeks; age 20 to 45 years; delivery of single or twin pregnancy; postpartum follow-up at 6 to 8 weeks, no severe pregnancy complications or comorbidities, and those who agree and voluntarily participate.

Exclusion criteria

Exclusion criteria: Exclusion criteria include a history of severe organ diseases; acute inflammation of the reproductive or urinary system; history of orthopedic trauma or surgery; history of mental illness; and those unwilling to participate in the study or unable to complete the study due to withdrawal during the process.

Design outcomes

Primary

MeasureTime frame
Pre-pregnancy body mass index;Pregnancy weight gain;Age;Pelvic floor muscle exercises within 6 weeks postpartum;Number of deliveries;Newborn birth weight;Mode of delivery;Duration of the second stage of labor;Postpartum Pelvic Floor Distress Inventory-20 (PFDI-20);Three-dimensional pelvic floor ultrasound data;Pelvic floor electromyography data;Pelvic Organ Prolapse Quantification;

Secondary

MeasureTime frame
Past smoking history;Past history of stress urinary incontinence;Stress urinary incontinence during pregnancy;Constipation during pregnancy;Pelvic floor muscle exercises in late pregnancy;Number of pregnancies;Delivery gestational week;Postpartum hemorrhage;PHQ-9 depression questionnaire;GAD-7 anxiety questionnaire;PHQ-15 somatic symptom questionnaire;

Countries

China

Contacts

Public ContactHua Zhang

Department of Obstetrics, The First Affiliated Hospital of Chongqing Medical University

zh2844@gmail.com+86 135 2742 6805

Outcome results

None listed

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