- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06611956
Needs Assessment Among Carers of Someone With Suicidal Thoughts
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
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Ghent, Belgium, 9000
- Flemish Centre of Expertise in Suicide Prevention, Ghent University
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
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
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Background information: information on the participant
Time Frame: Baseline. Completing the questionnaire will take about 15-20 minutes
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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)
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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
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Kessler Psychological Distress Scale , 6-item (Kessler et al., 2002, 2003)
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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
Sponsor
Investigators
- Principal Investigator: Gwendolyn Portzky, PhD, Flemish Centre of Expertise in Suicide Prevention (Ghent University)
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ONZ-2024-0404
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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