RecruitingNot ApplicableNCT07513077

Prevention of Noise-Induced Hearing Loss in Primary Education

Effectiveness of an Educational Program in Primary Schools to Prevent Noise-induced Hearing Loss


Sponsor

Erasmus Medical Center

Enrollment

600 participants

Start Date

Mar 30, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this randomized controlled trial is to evaluate the effectiveness of the educational program the HoorToren in promoting recreational safe listening behavior among Dutch primary school children in group 7 (aged 10-11 years) and thereby contribute to preventing noise-induced hearing loss. The main objectives are: * To evaluate the HoorToren's effects on promoting the child's safe listening behavior when using headphones or earbuds. Both safe listening and its psychological determinants will be measured. * To evaluate the HoorToren's effects on parents' perception of their child's safe listening behaviors. The effects on parental behavior promoting or facilitating their child's safe listening behavior, including its psychological determinants, will also be evaluated. Researchers will compare children who receive lessons from the HoorToren educational program, and their parents (intervention group) with children and their parents who do not receive the lessons (control group) to evaluate the effectiveness of the HoorToren. Outcomes will be assessed using newly developed and validated self-report questionnaires for both children and their parents. Additionally, the child's listening behavior will be measured via a smartphone application installed on the child's phone. Measurements will take place at four time points during the school year.


Eligibility

Inclusion Criteria6

  • For schools: None.
  • For children:
  • Dutch primary school children in group 7 (corresponding to Year 6 in the UK).
  • Informed consent from legally authorized parent(s) or guardian(s).
  • Parents:
  • Child is participating.

Exclusion Criteria7

  • For schools:
  • HoorToren package has been taught at group 6 in the previous school year.
  • For children:
  • Children without informed consent from legally authorized parent(s) or guardian(s).
  • Children who cannot read and write Dutch.
  • For parents:
  • Parents who cannot read and write Dutch

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

OTHERHoorToren educational package

Educational program, consisting of 7 classroom lessons for group 7. Each lesson has an average duration of 30-45 minutes. Parents are targeted in 4 home assignments for the children.


Locations(1)

Erasmus University Medical Center

Rotterdam, Netherlands

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07513077