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Improving Shared Decision-Making in Menstrual Management and Contraception for Adolescents and Young Adults | Clinical Trials | Clareo Health

RECRUITINGNA

Improving Shared Decision-Making in Menstrual Management and Contraception for Adolescents and Young Adults

Improving Shared Decision-Making in Menstrual Management and Contraception for Adolescents and Young Adults: A Cluster-Randomized Trial

NCT07320651•University Hospital, Geneva

View on ClinicalTrials.gov

Summary

Decision aids are educational tools designed to help people participate in decision-making about health care choices, by providing evidence-based information, promoting patient-centered care, and supporting patient autonomy and engagement. Our research team developed an Encounter Decision Aid (EDA) exploring treatment options for menstrual management in adolescents and young adults (AYAs), in accordance with the latest International Patient Decision Aids Standards and the Ottawa Decision Support Framework. In this cluster-randomized controlled trial, we aim to evaluate the effectiveness of this EDA on patient-centered outcome measures in AYAs considering treatment for menstrual management and/or contraception compared to standard counseling.

Eligibility

Age

12 - 25 years

Sex

FEMALE

Healthy Volunteers

Inclusion Criteria

•adolescents and young adults aged 12-25 years old
•presenting to an outpatient consultation at "Unité de policlinique de gynécologie" or "Consultation de gynécologie pédiatrique" at HUG
•considering initiation or switch to hormonal medication for menstrual management and/or contraception
•able to give informed consent as documented by signature or accompanied by a legal guardian who can provide consent if required.

Exclusion Criteria

•individuals who cannot read and understand French to a degree that would prevent participation in informed consent and study-related materials.
•individuals who have major sensory disability, such as visual or hearing impairment, that would compromise their ability to give written informed consent and use the EDA, in the absence of their legal guardian.
•individuals with cognitive or psychiatric conditions significantly impairing decision making capacity, unless accompanied by a legal guardian.
•patients currently participating in another clinical trial related to contraceptive decision-making, to avoid potential interference.

Locations (1)

Geneva University Hospitals

Geneva, Canton of Geneva, Switzerland

Key Dates

Start Date

September 2, 2025

Primary Completion Date

October 1, 2027

Completion Date

January 1, 2028

Last Updated

January 6, 2026

Enrollment

252

ESTIMATED participants

Conditions

ContraceptionMenstrual Management

Interventions

Encounter decision aid

OTHER

Standard counseling

OTHER

Contacts

Dehlia Moussaoui

CONTACT

+41 22 372 33 87 dehlia.moussaoui@hug.ch

Drospirenone Only Pills and Cervical Mucus Changes: A Pre- and Post-Bariatric Surgery Study

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Contraception

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RECRUITINGNA

Effect of Different Sex Hormone Profiles for the Response to Physical Training

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EumenorrheaIntrauterine Devices, Medicated+1 more

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 6, 2026Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Improving Shared Decision-Making in Menstrual Management and Contraception for Adolescents and Young Adults

Inclusion Criteria

Exclusion Criteria

Drospirenone Only Pills and Cervical Mucus Changes: A Pre- and Post-Bariatric Surgery Study

Effect of Different Sex Hormone Profiles for the Response to Physical Training

Study to Evaluate Contraceptive Efficacy and Safety of a Progestin Only Patch in Women of Childbearing Potential

Investigating Ovulation Inhibition for Use as a Contraceptive

Oral Contraceptive Pill (OCP) Pharmacogenomics

International Active Surveillance Study: Safety of Estrogen Estetrol (E4) Contraceptive Study (INAS-SEECS)