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New study sheds light on postpartum sexual struggles

NCT ID NCT07440082

Knowledge-focused Sponsor: Université de Reims Champagne-Ardenne Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study surveyed 80 women who gave birth 3 to 6 months earlier to learn about their experiences resuming sexual intercourse. Researchers aimed to identify common difficulties like pain, dryness, and low desire, and to improve how healthcare providers address sexual health after childbirth.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could help healthcare providers better support women's sexual health after childbirth.
What could go wrong
This is a small, completed survey study, so it only gathers information and does not test any treatment. Results may not apply to all women.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

80 people

The number who actually took part.

Started

Nov 2025

Finished

Jan 2026

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

women aged 18 and over, with a partner who gave birth more than 3 months and less than 6 months ago, regardless of the mode of delivery, whether or not they have resumed sexual intercourse since giving birth

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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)

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Conditions

The condition(s) this trial relates to.

Coitus

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Sexual intercourse

Contacts and locations

Locations

  • Ufr Medecine Urca

    Reims, 51100, France

More trials for these conditions

Other studies related to the condition(s) this trial covers.