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OpenTrials
Completed

NCT Number: NCT07440082

Resumption of Sexual Intercourse in the Postpartum Period: Women's Experiences

Sexual health, according to the World Health Organization (WHO), is a state of overall well-being related to sexuality. In the postpartum period, sexual health is often affected by hormonal, physical, and psychological changes. Up to 83% of women report sexual difficulties within the first three months after childbirth, and these issues may persist for up to a year. Dyspareunia is one of the most common symptoms, affecting approximately 35% of postpartum women. Other difficulties include vaginal dryness, fatigue, decreased libido, and fear of pain. Breastfeeding and perineal trauma are known to influence the resumption of sexual activity.

Health professionals may lack training or confidence in addressing sexual health, often leaving women to cope with their difficulties alone, even though they express a need for information and support. In this context, it is essential to better understand the difficulties women face when resuming sexual activity after childbirth, in order to improve the detection and management of sexual health disorders.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Observational

Primary location

Ufr Medecine Urca

Reims, 51100, France

About this study

Objectives Primary: To describe the resumption of sexual activity within the first 3 months postpartum, including any potential difficulties encountered.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women who gave birth between 3 and 6 months prior to participating in the study
  • Whether or not they have resumed sexual intercourse.
  • With a partner.
  • Aged 18 years or older
  • Agreeing to participate in the study.

Exclusion criteria

  • Women who were pregnant at the time of the study
  • Who had experienced perinatal bereavement
  • Who were protected by law (guardianship, curatorship, judicial protection)

Treatment and study plan

Data Collection

Other

data collection

Primary outcomes

  1. Questionnaire on the resumption of sexual intercourse in the postpartum period

    Time frame: Day0

    Proportion of participants who resumed sexual intercourse within the 3 months following childbirth

Sponsors and collaborators

Lead sponsor

Université de Reims Champagne-Ardenne

Other

Registry information

Acronym: RS-PP

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Feb 27, 2026
Registry last updated
Feb 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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