Preventing Violence by Teachers in Primary Schools in Haiti (ICC-T_HAITI)

July 26, 2023 updated by: Tobias Hecker, PhD, Bielefeld University

Preventing Violence by Teachers in Primary Schools in Haiti: A Cluster Randomized Controlled Trial of Interaction Competencies With Children - for Teachers (ICC-T)

Violence has severe and long-lasting negative consequences for children's and adolescents' well-being and academic functioning, which can hinder communities' and societies' economic growth. According to the Human Development Index, Haiti is one of the least developed countries in the world and the least developed in the Western hemisphere. Although Haiti has officially signed international and national laws aiming to protect children, preliminary reports suggest high rates of violence against children at schools. In addition to a lack of adequate training and supervision of teachers and an underdeveloped education system, attitudes favoring violence against children as an effective and acceptable discipline method and the lack of access to alternative non-violent strategies are likely to contribute to teachers' ongoing use of violence against children.

Notwithstanding, no school-level interventions addressing these factors to reduce violence by teachers have been scientifically evaluated in Haiti so far.

Thus, the present study tests the effectiveness of the preventative intervention Interaction Competencies with Children - for Teachers (ICC-T) in primary schools in Haiti. Previous studies have provided initial evidence on the feasibility and effectiveness of ICC-T to reduce teacher violence in primary and secondary schools in Tanzania and secondary schools in Uganda. This study aims to provide first evidence for the effectiveness of ICC-T to reduce violence and to improve children's functioning (i.e. mental health, well-being, academic performance) in a cultural setting outside of Sub-Saharan Africa.

Study Overview

Detailed Description

The study is designed as a two-arm cluster randomized controlled trial with schools (clusters) as level of randomization. The study will be conducted in the Northern department of Haiti. Six schools in each of the 6 included communes will be randomly selected, resulting in a total number of 36 schools.

In each commune, three schools will be randomly allocated to the intervention group (that will receive the ICC-T intervention) and three schools to the control group (that will receive no intervention). At each school, 28 students (stratified by gender) in the 4th grade of primary School (between 9 and 11 years of age) and all teachers (at least 13) will be recruited. Thus, the final sample will comprise at least 1008 students and at least 468 teachers.

The study will have two data assessment points: baseline assessment prior to the intervention and follow-up assessment six to 12 months after the intervention. In addition, feasibility data will be assessed in the intervention group at the beginning and the end of the intervention. Primary outcome measures are student- and teacher-reported physical and emotional violence by teachers in the past week. Secondary outcome measures include teachers' attitudes towards violence against students, children's emotional and behavioral problems, quality of life, and cognitive functioning.

Study Type

Interventional

Enrollment (Estimated)

1064

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

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

7 years to 70 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Written informed consent (if underaged by parents & minors themselves)

Students: Enrollment in class 4 of primary school

Teachers: All teachers employed at the school

Schools:

  • Public or community schools
  • Mixed-gender schools
  • Day schools
  • At least 40 students in selected class/stream

Exclusion Criteria:

Students and teachers:

  • Acute drug or alcohol intoxication
  • Acute psychotic disorder

Schools:

• Previous training on violence prevention

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: ICC-T
5 days with 9 hours of training for teachers. Core training components include teacher-student interaction, maltreatment prevention, effective discipline strategies, identifying and supporting burdened students and implementation of the training materials into the school setting

Core training components include teacher-student interaction, maltreatment prevention, effective discipline strategies, identifying and supporting burdened students and implementation of the training materials into the school setting.

A one-day ICC-T refresher workshop aiming to refresh and re-emphasize the key aspects of the intervention is implemented about 6 to 12 months after the initial intervention.

No Intervention: Monitoring condition
No intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of students' exposure to emotional and physical violence by teachers
Time Frame: The CTS will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)
The Conflict Tactics Scale (CTS) will be used to assess students' self-reported experiences of emotional and physical violence by teachers at school in the past week. Higher scores indicate higher levels of violence that is used by teachers. We hypothesize a stronger reduction of exposure to violence in the intervention group compared to the control group.
The CTS will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)
Change of teachers' use of emotional and physical violence
Time Frame: The CTS will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)
The Conflict Tactics Scale (CTS) will be used to assess teachers' use of emotional and physical violent discipline measures against students in the past week. Higher scores indicate higher levels of violence that is used by teachers. We hypothesize a stronger reduction of the use of violence in the intervention group compared to the control group.
The CTS will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of teachers' positive attitudes towards emotional and physical violence
Time Frame: The adapted version of CTS will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)
Teacher's attitudes towards emotional and physical violence will be assessed with an adapted version of the Conflict Tactic Scale (CTS). Higher scores indicate higher levels of positive attitudes towards violence. We hypothesize a stronger decrease of positive attitudes towards violence in the intervention group compared to the control group.
The adapted version of CTS will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)
Change of student's mental health
Time Frame: The PSC-Y will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)

The Pediatric Symptom Checklist - Youth Report (PSC-Y) will assess students' emotional and behavioral problems.

Higher scores indicate higher levels of students' mental health problems. We hypothesize a stronger reduction of mental health problems in the intervention group compared to the control group.

The PSC-Y will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)
Change of students' quality of life
Time Frame: The KIDSCREEN-10 will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)

The KIDSCREEN-10 will assess students' quality of life. Higher scores indicate higher levels of students' quality of life.

We hypothesize a stronger increase of quality of life in the intervention group compared to the control group.

The KIDSCREEN-10 will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)
Change of students' cognitive functioning
Time Frame: The app-based tasks will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)
Four tasks from the tablet application Psych Lab 101 will be used to assess children's cognitive abilities including selective attention, working memory, interference control and impulsivity. Higher scores indicate higher levels of students' cognitive abilities. We hypothesize higher levels of cognitive functioning in the intervention group compared to the control group.
The app-based tasks will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention)

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of students' academic performance
Time Frame: he standardized achievement tests will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention).
Purpose-built tests will be used to assess students' numeracy and literacy skills. Higher scores indicate higher levels of students' academic skills. In addition, students' grades in the previous term's exams will be obtained from the school administration. A change in academic performance in the intervention group is hypothesized.
he standardized achievement tests will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention).
Change of Students' social competence
Time Frame: The Social Cognitive Map Technique - peer nomination will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention).
The Social Cognitive Map Technique will assess students' social competence through peer nominations. Higher scores indicate higher levels of students' social competence. We hypothesize a stronger increase of social competence in the intervention group compared to the control group.
The Social Cognitive Map Technique - peer nomination will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention).
Change of peer violence
Time Frame: The Multidimensional Peer Victimization Scale will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention).
The Multidimensional Peer Victimization Scale will be used assess students' experiences of violence by peers. Higher scores indicate higher levels of students' experiences of peer violence. We hypothesize a stronger decrease of peer violence in the intervention group compared to the control group.
The Multidimensional Peer Victimization Scale will be used at T1 (baseline, prior to intervention) and T2 (follow-up, 6-12 months after intervention).

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Anke Hoeffler, Prof. Dr., University of Konstanz

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)

November 15, 2021

Primary Completion (Estimated)

December 31, 2024

Study Completion (Estimated)

July 31, 2025

Study Registration Dates

First Submitted

October 5, 2021

First Submitted That Met QC Criteria

October 5, 2021

First Posted (Actual)

October 18, 2021

Study Record Updates

Last Update Posted (Actual)

July 27, 2023

Last Update Submitted That Met QC Criteria

July 26, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • ICC-T_CRCT_Haiti

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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