Support for Parenthood: Education for the Emotional and Sexual Life of Adolescents Aged 11 to 15 Old (educ-parent)

February 24, 2026 updated by: Université de Reims Champagne-Ardenne

According to the WHO, sexual health is fundamental for human health and well-being. For this, it is necessary to talk about it from an early age: indeed, the place of parents is essential to bring education to sexuality with clear, scientific and true information.

Only a minority of parents manage to approach the prevention and promotion of emotional and sexual life, which leads to significant consequences.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The main objective is to describe the concepts discussed by parents with to their adolescents, aged 11 to 15 years old, female or male, elder of the siblings, regarding education for emotional and sexual life.

Study Type

Observational

Enrollment (Actual)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Reims, France, 51100
        • Ufr Medecine Urca

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Non-Probability Sample

Study Population

Parents of adolescents, male or female, aged 11 to 15 years old, elder of the siblings.

Description

Inclusion Criteria:

  • Parents (male or female) of adolescents aged 11 to 15 years old, female or male.
  • Having no older children meaning that the adolescent aged 11 to 15 is the eldest in the sibling order.
  • Agreeing to participate in the study

Exclusion Criteria:

  • Subjects protected by law (under guardianship, under curatorship, safeguarding of justice),
  • Subjects who refuse to participate in the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Questionnaire on the concepts covered in the field of sexual health
Time Frame: Day 0
The concepts addressed in the field of sexual health will be evaluated using a questionnaire specifically designed for the study by a team of midwives, methodologists, and a data manager. The questionnaire will include a series of yes/no questions covering topics such as: consent, respect for one's own body and that of others, equality between girls and boys, romantic relationships, the anatomy of male and female sexual organs and how they function (menstruation, erection, ejaculation), sexual orientation, desire, pleasure and sexual fulfillment, reproduction (fertilization and the risks of pregnancy), masturbation, foreplay and sexual relations, sexually transmitted infections, the different methods of contraception, voluntary interruption of pregnancy, and vigilance with regard to pornography, social networks and harassment.
Day 0

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2024

Primary Completion (Actual)

February 1, 2025

Study Completion (Actual)

July 1, 2025

Study Registration Dates

First Submitted

February 10, 2026

First Submitted That Met QC Criteria

February 24, 2026

First Posted (Actual)

March 2, 2026

Study Record Updates

Last Update Posted (Actual)

March 2, 2026

Last Update Submitted That Met QC Criteria

February 24, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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