CompletedNot Applicable

Knowledge About and Attitudes Towards Non-binary Persons in Flanders (Part 1: Quantitative Study)

Belgium2,000 participantsStarted 2025-08-04

Plain-language summary

The goal of this observational study is to investigate the knowledge about and attitudes towards non-binary individuals in Flemish adults. The main questions it aims to answer are: To which degree does the Flemish population have knowledge about non-binary persons? What are the attitudes of the Flemish population towards non-binary persons? What factors influence the attitudes towards non-binary persons? Furthermore, the aim is to create a survey to measure knowledge about and attitudes towards non-binary persons. Participants will complete an online survey.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 18+ years old * Living in Flanders or the Netherlands * enrolled in Ipsos ISO-certified panel Exclusion Criteria: * 17 or \<17 years old * not living in Flanders or the Netherlands * not enrolled in Ipsos ISO-certified panel

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Attitudes towards non-binary persons

Timeframe: At the time of enrollment

Trial details

NCT IDNCT07400887

SponsorUniversity Hospital, Ghent

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-08-18

View on ClinicalTrials.gov More Non-binary trials