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Educational Storytelling, an Innovative Interdisciplinary Program Against Child Maltreatment

NCT06599983 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 430

Last updated 2024-09-20

No results posted yet for this study

Summary

Educational Storytelling, an Innovative Novel Interdisciplinary Program Against Child Maltreatment, is developed for dental personnel. The program aims at increasing dental personnels ability to detect, report and treat patients being victims of child abuse or neglect.

The objectives of the program is to contribute to the fulfillment of the Norwegian:

* Dental health services act

§1-3 c The dental health service responsibility to prevent, detect and avert violence and sexual abuse
* Health Personnel act §33 Obligation to report suspected cases of child maltreatment to child welfare services.

The Educational Storytelling program aims to increase the dental health personnels knowledge and competence related to:

* Detecting child abuse and neglect.
* Reporting suspected cases of child maltreatment to child welfare services.
* Treatment of patients with known and unknown history of child abuse and neglect, trauma sensitive dental treatment.

The aim of this trial is to evaluate if the educational program has any effect.

Conditions

  • Child Abuse
  • Child Neglect
  • Child Sexual Abuse
  • Child Maltreatment
  • Oral Health
  • Dental Neglect

Interventions

OTHER

Educational program, Educational Storytelling, an Educational Program Against Child Abuse and Neglect.

One day educational program, aiming at increase dental personnels attitude, knowledge and behaviour in regard to detect and report child abuse and neglect, and to treat patients with known and unknown history of child abuse and neglect.

Sponsors & Collaborators

  • Educational storytelling forlag og film

    collaborator UNKNOWN

  • Oral Health Centre of Expertise in Western Norway

    lead OTHER

Principal Investigators

  • Ingfrid V Brattabø, PhD · Oral Health Centre of Expertice Western Norway

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-03-01
Primary Completion
2022-11-01
Completion
2022-11-01

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06599983 on ClinicalTrials.gov