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Establishment and clinical study of early accurate diagnosis and treatment technology for pelvic floor dysfunction

Establishment and clinical study of early accurate diagnosis and treatment technology for pelvic floor dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107578
Enrollment
Unknown
Registered
2025-08-14
Start date
2021-04-13
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

Pelvic Floor Dysfunction(PFD)

Interventions

control group:Aerobic exercise: 20 minutes of uniform running training three times a day for three weeks.
Pelvic floor muscle training group:1) Aerobic exercise: 20-minute steady running training three times a day for three weeks
2) Home pelvic floor muscle training: Training frequency is five days a week, three times a day, each time including rapid contraction, sustained contraction and coordination function training, with 2
Localized diagnosis and in-situ treatment technology group:1) Aerobic exercise: Three 20-minute steady running sessions per day for three consecutive weeks. 2) Home pelvic floor muscle training: Five

Sponsors

Women‘s Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 46 Years

Inclusion criteria

Inclusion criteria: Women between 42 days and 1 year postpartum, regardless of mode of delivery (vaginal or cesarean section); with intact cognitive and memory functions, as well as proficient Mandarin language expression skills; capable of performing basic physical activities or aerobic exercises, including maintaining a steady running pace for more than 30 minutes (at least three times per week for a minimum of one month); diagnosed with mild stress urinary incontinence according to established pelvic floor dysfunction criteria, with a total score of >= 3 on the International Consultation on Incontinence Questionnaire - Urinary Incontinence Short Form (ICIQ-UI-SF), and experiencing involuntary urinary leakage from the urethral meatus during physical activity or aerobic exercise; willing to participate in clinical observation and having signed the informed consent form.

Exclusion criteria

Exclusion criteria: Being pregnant or planning to become pregnant during the intervention; A history of hysterectomy or pelvic surgery (for urinary incontinence, anal incontinence, or pelvic organ prolapse); A musculoskeletal injury within the past 6 months that negatively affects exercise, and an inability to perform pelvic floor muscle contractions correctly; Patients with serious medical or surgical diseases; Damage, ulceration or infection at the treatment or testing site; Acute infection stage, high fever and coma; Patients with heart, liver and kidney dysfunction; Patients with a history of deep venous thrombosis of the lower extremities; Patients with malignant tumors and other chronic diseases; Vaginal bleeding, vaginitis; History of pelvic radiotherapy; Diseases of the nervous system that significantly affect muscle function; Patients with a history of neurologic or psychiatric problems who were deemed by the investigator to be ineligible for participation in the trial.

Design outcomes

Primary

MeasureTime frame
Pelvic floor muscle strength;Fatigue of the pelvic floor muscles;Pelvic floor muscle coordination;

Secondary

MeasureTime frame
Urinary incontinence related questionnaire score;

Countries

China

Contacts

Public ContactXie Zhenwei

Women‘s Hospital, School of Medicine, Zhejiang University

xiezw@zju.edu.cn+86 135 8803 0456

Outcome results

None listed

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