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Construction and Application Research of multi-component Exercise Intervention Program for Patients with postpartum pelvic Floor dysfunction

Construction and Application Research of multi-component Exercise Intervention Program for Patients with postpartum pelvic Floor dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500109486
Enrollment
Unknown
Registered
2025-09-19
Start date
2025-09-19
Completion date
Unknown
Last updated
2025-09-22

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

Conditions

Pelvic floor dysfunction

Interventions

Control group:Health education + pelvic floor muscle training
Experimental Group:Health education + pelvic floor muscle training + multi-component exercise

Sponsors

Hunan University of Technology
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
22 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for pelvic floor dysfunction set by the International Association of Urology and Gynecology (IUGA) and the International Incontinence Society (ICS); 2. Women aged 22 to 45, who have been postpartum for at least 42 days but less than one year; 3. The parturient must be in good health, free from a history of chronic cough, asthma, long-term constipation or chronic pelvic pain, as well as chronic diseases such as urinary tract infection, diabetes, hypertension and kidney disease. 4. No history of pelvic surgery (except cesarean section); 5. Good compliance, voluntary participation in this trial and signing of the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Underlying diseases that affect the progress of training, such as epilepsy, myocardial infarction, heart failure history, and severe lung infection; 2. Accompanied by severe malformations of the lower extremity anatomical structure; 3. Subjects with incomplete lochia after childbirth, infection or inflammation in the perineum or sacrum; 4. Those who have cognitive or communication impairments and are unable to cooperate with assessment and treatment; 5. Subjects who are currently participating in other sports clinical trials; 6. Other circumstances where the researcher assesses that the subject is not suitable to participate in this trial.

Design outcomes

Primary

MeasureTime frame
Score of the brief Form of the Pelvic Floor Discomfort Questionnaire;The modified Oxford scale;

Secondary

MeasureTime frame
Pelvic organ prolapse quantitation;Electromyography test of the pelvic floor muscles;One-hour pad test;

Countries

China

Contacts

Public ContactWang Shiqiang

Hunan University of Technology

yeslllyyy@163.com+86 22182968

Outcome results

None listed

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