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Effect observation of pelvic floor electrical stimulation combined with biofeedback in the treatment of postpartum sexual dysfunction and pelvic floor dysfunction

Effect observation of pelvic floor electrical stimulation combined with biofeedback in the treatment of postpartum sexual dysfunction and pelvic floor dysfunction

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071886
Enrollment
Unknown
Registered
2023-05-29
Start date
2023-06-01
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Sexual dysfunction, pelvic floor dysfunction

Interventions

experimental group:Pelvic floor electrical stimulation combined with biofeedback
control group:Self propelled pelvic floor muscle training

Sponsors

University of Hong Kong Shenzhen Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Pregnant women who undergo prenatal examination and delivery at our hospital for 6-12 weeks postpartum. 2. The newborn is single and normal. 3. The subjects had normal cognitive abilities and voluntarily participated in this study with informed consent.

Exclusion criteria

Exclusion criteria: (1) Vaginal dystocia, vaginal midwifery. (2) Acute genital tract inflammation, postpartum lochia not clean. (3) Unwilling to participate in this study. (4) high-risk pregnant women, including: multiple pregnancies, pelvic abnormalities, soft birth canal abnormalities, obvious genital development abnormalities, heart disease, hepatitis, etc (5) postpartum depression and other postpartum mental disorders. (6) At present, one of the husband and wife has a serious and unstable physical disease and has a significant impact on sexual function, such as brain organ disease, cardiovascular disease, endocrine disease, immune system disease, kidney disease. (7) A history of trauma and surgery affecting sexual life. (8) severe urinary incontinence, fecal incontinence, or pelvic organ prolapse.

Design outcomes

Primary

MeasureTime frame
Pelvic floor electrophysiological indicators;Female Sexual Function Index questionnaire (FSFI);Pelvic floor dysfunction questionnaire (PFDI-20);Pelvic floor obstruction impact brief questionnaire(PFIQ-7);

Secondary

MeasureTime frame
Pelvic floor organ prolapse grading(POP-Q);

Countries

China

Contacts

Public ContactChaoxia Lyu

University of Hong Kong Shenzhen Hospital

lvcx@hku-szh.org+86 136 3299 8546

Outcome results

None listed

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