Management of Post-delivery Pain and Its Impact on Resumption of Sexuality
Completed
- Conditions
- SexualityDelivery
- Registration Number
- NCT03953573
- Lead Sponsor
- Hopital Foch
- Brief Summary
Study of management of pain and information given to women post-delivery and their impact of the resumption of sexuality.
Survey to be completed by women at 8 and 15 days and 1 or 3 months after delivery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 105
Inclusion Criteria
- Primiparous woman
- Age between 18 and 45 years old
- Delivery after 37 weeks of amenorrhea
- Speaking French
- Pregnancy, delivery and new-born examination without morphologic or biometric abnormalities, respiratory distress and no pathology discovered at neonatal screening on day 3
- Heterosexual woman with partner
- Signed consent
- Affiliate of national health insurance scheme
Exclusion Criteria
- Multiple pregnancy,
- BMI > 30
- Conjugopathie
- Known psychiatric history
- Medical history with gynecologic impact
- Surgery history with gynecologic impacts
- Hysterectomy post-delivery
- Protected by French law
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post-delivery sexuality resumption 3 months Time to sexuality resumption
- Secondary Outcome Measures
Name Time Method Sexual health 3 months Frequency of sex
Discussion with healthcare professional on post-delivery sexuality 1 month Number of women receiving advice from a health professional
Pain post-delivery 3 months Number of women needed pain treatment or with problem for sexuality resumption
Trial Locations
- Locations (1)
Hopital Foch
🇫🇷Suresnes, France
Hopital Foch🇫🇷Suresnes, France