NCT05924217

Brief Summary

In France, cervical cancer screening is the subject of a national screening programme organized for all asymptomatic individuals aged 25 to 65 years with a cervix. The latter contributes greatly to the prevention and early treatment of this disease, whose public health challenge is recognized worldwide. One of the objectives of this programme is to reduce inequalities in access. Transgender men, i.e. individuals assigned to the female gender at birth but identifying with the male gender, are concerned by this screening as long as they still have a cervix, according to the same modalities as for cisgender women. However, they are often excluded from health care, including organized screening programs. Gender change in civil status is one of the obstacles. The provision of gynaecological care is sometimes inadequate. The lack of knowledge of health professionals and the problems of discrimination that transgender people may face reduce the chances of having equitable access. This survey aims to explore the perception that transgender men have of cervical cancer screening and to identify the challenges they face, the obstacles and the levers to access this prevention program.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for all trials

Timeline
1mo left

Started Jan 2024

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress94%
Jan 2024Jun 2026

First Submitted

Initial submission to the registry

June 12, 2023

Completed
17 days until next milestone

First Posted

Study publicly available on registry

June 29, 2023

Completed
6 months until next milestone

Study Start

First participant enrolled

January 2, 2024

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2025

Completed
1.5 years until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Expected
Last Updated

November 17, 2025

Status Verified

November 1, 2025

Enrollment Period

1 year

First QC Date

June 12, 2023

Last Update Submit

November 14, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • prevalence of transgender men who have ever been screened for cervical cancer in their lifetime

    answer yes to the question "Have you ever been screened for cervical cancer in your lifetime?"

    At study entry, basline (no follow-up)

Secondary Outcomes (1)

  • prevalence of transgender men who feel concerned about cervical cancer screening

    At study entry, basline (no follow-up)

Interventions

This survey aims to explore the perception that transgender men have of cervical cancer screening and to identify the challenges they face, the obstacles and the levers to access this prevention program.

Eligibility Criteria

Age25 Years - 65 Years
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Transgender men, i.e. individuals assigned the female gender at birth but identifying with the male gender, who retained the cervix

You may qualify if:

  • transgender male (assigned female at birth but identifying as male)
  • aged 25 to 65 years
  • Having retained her cervix
  • Having had sex before.

You may not qualify if:

  • Under 25 and over 65
  • Not having retained his cervix
  • History of cancerous lesion of the cervix

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU de Nîmes

Nîmes, 30900, France

Location

MeSH Terms

Conditions

Uterine Cervical Neoplasms

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Uterine NeoplasmsGenital Neoplasms, FemaleUrogenital NeoplasmsNeoplasms by SiteNeoplasmsUterine Cervical DiseasesUterine DiseasesGenital Diseases, FemaleFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesGenital Diseases

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • ingrid JULIER

    Centre Hospitalier Universitaire de Nīmes

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 12, 2023

First Posted

June 29, 2023

Study Start

January 2, 2024

Primary Completion

January 1, 2025

Study Completion (Estimated)

June 30, 2026

Last Updated

November 17, 2025

Record last verified: 2025-11

Locations