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Efficacy of Kegel Exercises Combined with Biofeedback Electrical Stimulation in the Rehabilitation of Perimenopausal Women with Stress Urinary Incontinence

Efficacy of Kegel Exercises Combined with Biofeedback Electrical Stimulation in the Rehabilitation of Perimenopausal Women with Stress Urinary Incontinence

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600129266
Enrollment
Unknown
Registered
2026-08-03
Start date
2026-08-07
Completion date
Unknown
Last updated
2026-08-10

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

Conditions

Stress urinary incontinence

Interventions

Experimental group:Kegel Training combined with Biofeedback Electrical Stimulation
Control Group 1:Kegel exercises
Control Group 2:Simple pelvic floor electrical stimulation

Sponsors

Hangzhou First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
40 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for perimenopause (age 40-60 years old, accompanied by menstrual disorders or with a duration of menopause less than 1 year); 2. Diagnosed with SUI: experiences involuntary urine leakage when abdominal pressure increases such as during coughing, laughing or sneezing, while there is no leakage under normal circumstances; 3. Evaluated as mild to moderate SUI by the ICI-Q-SF score; 4. Had no history of related menopausal medication or treatment related to SUI within 3 months before enrollment; 5. 18.5 kg/m^2 <= BMI <= 24.9 kg/m^2; 6. Completely voluntarily participated in the examination and treatment process and signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. History of pelvic surgeries such as after hysterectomy, vaginal surgery or surgery for urinary incontinence correction; 2. Pelvic organ prolapse (uterine prolapse, bladder prolapse, rectal prolapse); 3. Musculoskeletal disorders or collagen disorder; 4. Comorbid chronic diseases such as hypertension, diabetes, constipation, etc.; 5. Comorbid organic diseases of the heart, lungs, liver, and kidneys; 6. Individuals with cognitive impairment who cannot cooperate with examinations and treatments.

Design outcomes

Primary

MeasureTime frame
International Consultation on Incontinence Questionnaire - Short Form,ICI-Q-SF;Glazer protocol-based pelvic floor sEMG.;Pelvic Floor Ultrasonography;

Secondary

MeasureTime frame
Pittsburgh Sleep Quality Index;Incontinence Quality of Life Questionnaire,I-QOL;Blood Biomarkers;Anxiety and Depression Assessment;Musculoskeletal Fitness;

Countries

China

Contacts

Public ContactXiaowei Ding

Hangzhou First People's Hospital

xiaoweiding612@163.com+86 571 5812 9809

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026