Needs Assessment Among Carers of Someone With Suicidal Thoughts

August 28, 2025 updated by: University Ghent

With this study the investigators would like to gain insight into the experienced needs carers of individuals with suicidal thoughts, who attempted suicide or who died by suicide. By carers the investigators mean everyone who knows/knew someone close to them who is thinking about suicide, attempted suicide or died by suicide. By mapping out these needs, the investigators hope to better support carers and develop/improve initiatives and tools.

The investigators examine this by means of an online one-time questionnaire. In this questionnaire the investigators ask the participants questions about what it is like to be a carer and what are some of the experienced needs, as well as experiences with existing initiatives/tools.

Study Overview

Study Type

Observational

Enrollment (Actual)

2255

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

      • Ghent, Belgium, 9000
        • Flemish Centre of Expertise in Suicide Prevention, Ghent University

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Participants are inidividuals (16 years or older) who know someone close to them with suicidal thoughts and/or behaviors in the past three years.

Description

Inclusion Criteria:

  • 16 years or older
  • Someone close to them has experienced suicidal thoughts, attempted suicide or died by suicide in the past three years
  • Access to internet
  • Understand sufficient Dutch (to complete the questionnaire)

Exclusion Criteria:

  • /

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
Background information: information on the participant
Time Frame: Baseline. Completing the questionnaire will take about 15-20 minutes
Personal information (self-developed questionnaire): age, gender identity, education, cultural background, work status, recruitment type
Baseline. Completing the questionnaire will take about 15-20 minutes
Background information: information on the suicidal person
Time Frame: Baseline. Completing the questionnaire will take about 15-20 minutes
Information on the suicidal person (self-developed questionnaire): relationship with the person, age, gender identity, suicidality, degree of contact
Baseline. Completing the questionnaire will take about 15-20 minutes
Experienced burden: suicidality
Time Frame: Baseline. Completing the questionnaire will take about 15-20 minutes
based on national health survey (Sciensano, 2018)
Baseline. Completing the questionnaire will take about 15-20 minutes
Experienced burden when supporting the individual with suicdial thoughts
Time Frame: Baseline. Completing the questionnaire will take about 15-20 minutes
self-developed questionnaire on the role of the carer and current degree of care
Baseline. Completing the questionnaire will take about 15-20 minutes
Experienced burden when supporting the individual with suicdial thoughts
Time Frame: Baseline. Completing the questionnaire will take about 15-20 minutes
Zarit Caregiver Burden 4-item questionnaire (Zarit et al., 1985; Higginson et al., 2010)
Baseline. Completing the questionnaire will take about 15-20 minutes
Experienced burden: psychological stress
Time Frame: Baseline. Completing the questionnaire will take about 15-20 minutes
Kessler Psychological Distress Scale , 6-item (Kessler et al., 2002, 2003)
Baseline. Completing the questionnaire will take about 15-20 minutes
Experienced needs
Time Frame: Baseline. Completing the questionnaire will take about 15-20 minutes
Self-developed questionnaire examining the need for information, need for support and needs with regards to health care
Baseline. Completing the questionnaire will take about 15-20 minutes
Experience with existing initiatives and tools
Time Frame: Baseline. Completing the questionnaire will take about 15-20 minutes
Self-developed questionnaire about the experience of participants with existing initiatives and tools
Baseline. Completing the questionnaire will take about 15-20 minutes

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Gwendolyn Portzky, PhD, Flemish Centre of Expertise in Suicide Prevention (Ghent University)

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)

November 29, 2024

Primary Completion (Actual)

May 12, 2025

Study Completion (Actual)

May 12, 2025

Study Registration Dates

First Submitted

September 4, 2024

First Submitted That Met QC Criteria

September 20, 2024

First Posted (Actual)

September 25, 2024

Study Record Updates

Last Update Posted (Estimated)

September 5, 2025

Last Update Submitted That Met QC Criteria

August 28, 2025

Last Verified

August 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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