NCT06611956

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
2,255

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Nov 2024

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

First Submitted

Initial submission to the registry

September 4, 2024

Completed
21 days until next milestone

First Posted

Study publicly available on registry

September 25, 2024

Completed
2 months until next milestone

Study Start

First participant enrolled

November 29, 2024

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 12, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 12, 2025

Completed
Last Updated

September 5, 2025

Status Verified

August 1, 2025

Enrollment Period

5 months

First QC Date

September 4, 2024

Last Update Submit

August 28, 2025

Conditions

Keywords

needs assessmentinformal caregiverssuicide

Outcome Measures

Primary Outcomes (8)

  • Background information: information on the participant

    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

    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

    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

    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

    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

    Kessler Psychological Distress Scale , 6-item (Kessler et al., 2002, 2003)

    Baseline. Completing the questionnaire will take about 15-20 minutes

  • Experienced needs

    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

    Self-developed questionnaire about the experience of participants with existing initiatives and tools

    Baseline. Completing the questionnaire will take about 15-20 minutes

Interventions

No intervention (observational study)

Eligibility Criteria

Age16 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-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.

You may qualify if:

  • 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)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Flemish Centre of Expertise in Suicide Prevention, Ghent University

Ghent, 9000, Belgium

Location

MeSH Terms

Conditions

Suicide PreventionSuicide

Interventions

Observation

Condition Hierarchy (Ancestors)

Self-Injurious BehaviorBehavioral SymptomsBehavior

Intervention Hierarchy (Ancestors)

MethodsInvestigative Techniques

Study Officials

  • Gwendolyn Portzky, PhD

    Flemish Centre of Expertise in Suicide Prevention (Ghent University)

    PRINCIPAL INVESTIGATOR

Study Design

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

Study Record Dates

First Submitted

September 4, 2024

First Posted

September 25, 2024

Study Start

November 29, 2024

Primary Completion

May 12, 2025

Study Completion

May 12, 2025

Last Updated

September 5, 2025

Record last verified: 2025-08

Data Sharing

IPD Sharing
Will not share

Locations