- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07365891
Recognizing Emotional Neglect and Help-Seeking Intention Among Adolescents in Brussels
Help-Seeking Behavior in Cases of Emotional Neglect: The Decision-Making Process of Adolescents in Dutch-Speaking Secondary Education in Brussels
The goal of this study is to find out how well adolescents in Dutch-speaking secondary schools in Brussels can recognize emotional neglect, and how this relates to their intention to seek help.
The main research questions are:
- How well do adolescents recognize situations of emotional neglect, and do boys and girls differ in their recognition?
- Does recognition of emotional neglect predict adolescents' intention to seek help?
This study is conducted through an online survey. Participants will read one of four short written stories about an adolescent experiencing emotional neglect. The stories vary by gender (boy or girl) and by the clarity of the neglect (clear or ambiguous). After reading, participants answer questions about the story, including their thoughts and how they might respond in a similar situation. They also answer questions about their own experiences and attitudes toward help-seeking.
Study Overview
Status
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Fiona Roulent
- Phone Number: +32 2 629 36 52
- Email: Fiona.Madona.Roulent@vub.be
Study Contact Backup
- Name: Johan Vanderfaeillie
- Email: Johan.Vanderfaeillie@vub.be
Study Locations
-
-
Brussels Capital
-
Brussels, Brussels Capital, Belgium, 1050
- Recruiting
- Vrije Universiteit Brussel
-
Contact:
- Fiona Roulent
- Phone Number: +32 2 629 36 52
- Email: Fiona.Madona.Roulent@vub.be
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Age: adolescents aged 11-25 years;
- Education: enrolled in regular full-time secondary education;
- School location: Brussels-Capital Region;
- School language: Dutch;
- Consent: informed consent provided by the adolescent and their parent(s)/guardian.
Exclusion Criteria:
- Age: younger than 11 years or older than 25 years;
- Education: not enrolled in regular full-time secondary education;
- School location: outside the Brussels-Capital Region;
- School language: non - Dutch-speaking;
- Consent: informed consent not provided by the adolescent or their parent(s)/guardian.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: boy x clear situation
Participants are exposed to a vignette describing a boy in a clear emotional neglect situation.
|
Participants are randomly assigned to one of four written vignettes of adolescents experiencing emotional neglect.
Each vignette differs by gender (boy or girl) and by situation clarity (ambiguous or clear).
|
|
Experimental: boy x ambiguous situation
Participants are exposed to a vignette describing a boy in a ambiguous emotional neglect situation.
|
Participants are randomly assigned to one of four written vignettes of adolescents experiencing emotional neglect.
Each vignette differs by gender (boy or girl) and by situation clarity (ambiguous or clear).
|
|
Experimental: girl x ambiguous situation
Participants are exposed to a vignette describing a girl in a ambiguous emotional neglect situation.
|
Participants are randomly assigned to one of four written vignettes of adolescents experiencing emotional neglect.
Each vignette differs by gender (boy or girl) and by situation clarity (ambiguous or clear).
|
|
Experimental: girl x clear situation
Participants are exposed to a vignette describing a girl in a clear emotional neglect situation.
|
Participants are randomly assigned to one of four written vignettes of adolescents experiencing emotional neglect.
Each vignette differs by gender (boy or girl) and by situation clarity (ambiguous or clear).
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Help-seeking intention
Time Frame: Immediately after reading the vignette
|
Help-seeking intention is measured by asking participants to indicate whether they would seek help in the situation described in the vignette, using a 4-point Likert scale (1 = definitely not, 2 = probably not, 3 = probably yes, 4 = definitely yes). Higher scores indicate greater intention to seek help. Scores will be analyzed using linear regression, with recognition as the independent variable and help-seeking intention as the dependent variable. Additional analyses will test whether perceived severity and anticipated risk of future harm moderate the relationship between recognition and help-seeking intention. |
Immediately after reading the vignette
|
|
Recognition of emotional neglect
Time Frame: Immediately after reading the vignette
|
Recognition is measured by asking participants to indicate whether emotional neglect is present in the vignette, using a 4-point Likert scale (1 = definitely not, 2 = probably not, 3 = probably yes, 4 = definitely yes). Higher scores indicate greater recognition of emotional neglect. Scores will be analyzed using analysis of covariance (ANCOVA) with age as a covariate. Factors include participant gender (boy or girl), vignette gender (boy or girl), and type of situation (ambiguous or clear). Exploratory analyses may examine recognition of other types of maltreatment (physical abuse, physical neglect, emotional abuse, and sexual abuse). |
Immediately after reading the vignette
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Severity
Time Frame: Immediately after reading the vignette
|
Severity is measured by asking participants to indicate how severe they perceived the situation described in the vignette, using a 4-point Likert scale (1 = not at all severe, 2 = not severe, 3 = severe, 4 = very severe).
Higher scores indicate greater perceived severity.
|
Immediately after reading the vignette
|
|
Risk of future harm
Time Frame: Immediately after reading the vignette
|
Risk of future harm is measured by asking participants to estimate the probability that the adolescent in the vignette will experience future physical or emotional problems.
Each type of problem is rated on a 6-point Likert scale (1 = no chance, 2 = very small chance, 3 = small chance, 4 = moderate chance, 5 = large chance, 6 = very large chance).
Higher scores indicate greater anticipated risk of future harm.
|
Immediately after reading the vignette
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
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
- 25276_Hulpzoekgedrag
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
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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