Sexual dysfunction, pelvic floor dysfunction
Conditions
Interventions
Sponsors
Eligibility
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
| Measure | Time 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
| Measure | Time frame |
|---|---|
| Pelvic floor organ prolapse grading(POP-Q); | — |
Countries
China
Contacts
University of Hong Kong Shenzhen Hospital