User feedback on Zelfmoord1813.be and related websites

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational project monitors the availability, accessibility, and user experience of Zelfmoord1813.be and three related Flemish suicide-prevention websites. Researchers invite people aged 16 and older who have visited any of these sites to provide feedback and may combine user surveys with technical checks of site access and resource visibility. The work focuses on crisis access (phone, chat, email), clarity of information for different audiences (public, professionals, journalists), and barriers to finding help. The study is led by Ghent University and coordinated through the Flemish Centre of Expertise in Suicide Prevention in Ghent.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 16 y/o or older
* visit(ed) websites zelfmoord1813.be, mee-leven.be, werkgroepverder.be or komuitjekop.be

Exclusion Criteria:

* /

Where it's running

• Flemish Centre of Expertise in Suicide Prevention
  Ghent, Belgium Recruiting

Study contacts

• Principal investigator: Gwendolyn Portzky, PhD — University Ghent
• Study coordinator: Eva De Jaegere, PhD
• Email: eva.dejaegere@ugent.be
• Phone: +32 (0)9 332.07.75

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Other studies for the same condition or treatment. Recruiting studies are listed first.

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.