Recognizing Emotional Neglect and Help-Seeking Intention Among Adolescents in Brussels

April 27, 2026 updated by: Fiona Roulent, Vrije Universiteit Brussel

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:

  1. How well do adolescents recognize situations of emotional neglect, and do boys and girls differ in their recognition?
  2. 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

Study Type

Interventional

Enrollment (Estimated)

500

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Brussels Capital
      • Brussels, Brussels Capital, Belgium, 1050

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

Accepts Healthy Volunteers

Yes

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

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

  • 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

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

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)

February 23, 2026

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

June 1, 2026

Study Registration Dates

First Submitted

January 16, 2026

First Submitted That Met QC Criteria

January 16, 2026

First Posted (Actual)

January 26, 2026

Study Record Updates

Last Update Posted (Actual)

April 28, 2026

Last Update Submitted That Met QC Criteria

April 27, 2026

Last Verified

January 1, 2026

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

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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