To Increase Psychological Well-being by the Implementation of Forgiveness Education

August 3, 2022 updated by: University of Wisconsin, Madison

Implementation of Forgiveness Education to Increase Psychological Well-being in Three Culturally Distinct Areas: Northern Ireland, Israel/Palestine, and Taiwan

This project examines the development of psychological well-being in children and teachers through a 12- week forgiveness education program conducted in three conflict zones of the world, Northern Ireland, Israel/Palestine, and Taiwan.

A 12-week forgiveness education program will be investigated in elementary schools in three conflict zones of the world, Northern Ireland, Israel/Palestine, and Taiwan. The responsibilities of the sub-team in each of the three research sites will be:

  • a. recruiting schools, assisting the teacher training before the forgiveness education program starts
  • b. shepherding teachers, doing the fidelity checks, administering the instruments and collecting data during the forgiveness education program.

Once a school gives permission to be part of this study, the forgiveness curriculum will be implemented as a 12-week standard curriculum for the grade 5 (US equivalency) students. Teachers of the grade 5 classes will be trained to administer the program. Teachers, students and their parents must give the consent to take part in the measures of the study.

Study Overview

Status

Completed

Detailed Description

Classrooms participating in this study will be randomly assigned to either an experimental or a control group. The experimental group will receive the 1st forgiveness intervention for 12 weeks and then the control group will turn into an experimental group to receive a 2nd forgiveness intervention for 12 weeks.

In order to assess if such education increases psychological well-being in students (children) and teachers (adults), teachers and students in both groups will receive the same measures for four times in the study: within one week before the 1st forgiveness intervention, within one week after the 1st forgiveness intervention, within one week after the 2nd forgiveness intervention, four weeks after the 2nd forgiveness intervention.

The instruments include: for teachers, the assessment data will consist of the Enright Forgiveness Inventory Short Form (EFI-30), the Patient-Reported Outcomes Measurement Information System (PROMIS): Anger, Anxiety, and Depression scales, the Ethnic Prejudice Scale, the Herth Hope Index, the Rosenberg Self-Esteem Scale, a Classroom Cooperation scale, and a Cross-Cultural Exit Interview (written questionnaire). For students, the assessment data will consist of the Enright Forgiveness Inventory for Children (EFI-C), the PROMIS measures for pediatric self-report (ages 8-17): Anger, Anxiety, and Depressive Symptoms scales, the Ethnic Prejudice Scale for children, the Children's Hope Scale, the Coopersmith Self-Esteem Inventory (School Form), and academic achievement (likely to be scores/grades of Math, writing and reading in their own language). After the 2nd forgiveness intervention, select participants (teachers and children) will take part in individual interviews.

Study Type

Interventional

Enrollment (Actual)

1300

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 Locations

    • Wisconsin
      • Madison, Wisconsin, United States, 53706
        • University of Wisconsin-Madison

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

10 years to 65 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Students in 5th grade (US equivalency, aged 10-12)
  • Teachers in 5th grade (US equivalency)

Exclusion Criteria:

  • Students who are in grades other than 5th grade
  • Teachers who are in grades other than 5th grade

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Forgiveness curriculum for 5th grade
Classrooms randomly assigned to the experimental group will receive the forgiveness intervention. The forgiveness intervention will follow the curriculum - "The Journey Toward Forgiveness -A Guided Curriculum for Children Ages 10-12 (Grade 5 in the US)". The Forgiveness Curriculum Guide consists 14 lessons over 12 weeks. Each class meets weekly for 40 to 60 minutes to complete one lesson (in two of the weeks, there will be two lessons).
The forgiveness education intervention primarily teaches the concept of forgiveness through stories. We chose the kind of stories that should appeal to children ages 10 through 12. Each lesson is planned according to the following procedure: story-telling/movie-watching, discussion, and in-class activities.
No Intervention: Regular school instruction
Classrooms randomly assigned to the control group will have instruction as usual.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in forgiveness in adult (teachers) after forgiveness intervention assessed by EFI-30.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Enright Forgiveness Inventory Short Form (EFI-30), scores range from 30 to 180 with higher scores representing higher levels of forgiveness, which is a better outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in forgiveness in child (students) after forgiveness intervention assessed by EFI-C.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Enright Forgiveness Inventory for Children (EFI-C): scores range from 30 to 120 with higher scores representing higher levels of forgiveness, which is a better outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in anger in adult (teachers) after forgiveness intervention assessed by PROMIS Measures.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
The Patient Reported Outcome Measurement Information System (PROMIS) Anger Short Form: scores range from 5 to 25 with higher scores representing higher levels of anger, which is a worse outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in anger in child (students) after forgiveness intervention assessed by PROMIS Measures.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
The Patient Reported Outcome Measurement Information System (PROMIS) Measures for Pediatric (ages 8-17) Anger Short Form: scores range from 5 to 25 with higher scores representing higher levels of anger, which is a worse outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in anxiety in adult (teachers) after forgiveness intervention assessed by PROMIS Measures.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
The Patient Reported Outcome Measurement Information System (PROMIS) Anxiety Short Form: scores range from 5 to 40 with higher scores representing higher levels of anxiety, which is a worse outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in anxiety in child (students) after forgiveness intervention assessed by PROMIS Measures.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
The Patient Reported Outcome Measurement Information System (PROMIS) Measures for Pediatric (ages 8-17) Anxiety Short Form: scores range from 5 to 40 with higher scores representing higher levels of anxiety, which is a worse outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in depression in adult (teachers) after forgiveness intervention assessed by PROMIS Measures.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
The Patient Reported Outcome Measurement Information System (PROMIS) Depression Short Form, scores range from 5 to 40 with higher scores representing higher levels of depression, which is a worse outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in depression in child (students) after forgiveness intervention assessed by PROMIS Measures.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
The Patient Reported Outcome Measurement Information System (PROMIS) Measures for Pediatric (ages 8-17) Depressive Symptoms Short Form: scores range from 5 to 40 with higher scores representing higher levels of depression, which is a worse outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in prejudice in adult (teachers) after forgiveness intervention assessed by the Ethnic Prejudice Scales.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
The Ethnic Prejudice Scale: scores range from 20 to 100 with higher scores representing higher levels of prejudice, which is a worse outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in prejudice in child (students) after forgiveness intervention assessed by the Ethnic Prejudice Scales.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Ethnic Prejudice Scales: wording changes in the adult form of the Ethnic Prejudice Scale will be made to bring it to the level of 5th grade students (aged 10-12). Scores range from 20 to 100 with higher scores representing higher levels of prejudice, which is a worse outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in hope in adult (teachers) after forgiveness intervention assessed by Herth Hope Index.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Herth Hope Index: scores range from 12 to 48 with higher scores representing more hopefulness, which is a better outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in hope in child (students) after forgiveness intervention assessed by Children's Hope Scale.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
The Children's Hope Scale: scores range from 6 to 36with higher scores representing more hopefulness, which is a better outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in self-esteem in adult (teachers) after forgiveness intervention assessed by the Rosenberg Self-Esteem Scale.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
The Rosenberg Self-Esteem Scale: scores range from 10 to 40 with higher scores representing higher self-esteem, which is a better outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in self-esteem in child (students) after forgiveness intervention assessed by the Coopersmith Self-Esteem Inventory.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Coopersmith Self-Esteem Inventory Short Form: scores range from 0 to 25 with higher scores representing higher self-esteem, which is a better outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
Change in classroom cooperation in students after forgiveness intervention assessed by the Classroom Cooperation Scale.
Time Frame: Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.
The Classroom Cooperation Scale is teachers' measure of student cooperation, scores range from 10 to 40 with higher scores representing higher level of cooperation, which is a better outcome.
Baseline, up to 14 weeks, up to 31 weeks, up to 34 weeks.

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Robert W Enright, PhD, University of Wisconsin, Madison

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

September 3, 2021

Primary Completion (Actual)

July 31, 2022

Study Completion (Actual)

July 31, 2022

Study Registration Dates

First Submitted

May 21, 2020

First Submitted That Met QC Criteria

May 21, 2020

First Posted (Actual)

May 27, 2020

Study Record Updates

Last Update Posted (Actual)

August 4, 2022

Last Update Submitted That Met QC Criteria

August 3, 2022

Last Verified

August 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 2020-0432
  • A173000 (Other Identifier: UW Madison)
  • EDUC/EDUC PSYCH (OTHER: University of Wisconsin, Madison)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Plan Description

The individual participant data (IPD) that underlie the results reported in this article, after de-identification (text, tables, figures, and appendices).

IPD Sharing Time Frame

The IPD will be shared beginning 1 year and ending 5 years following the first article publication, with anyone who wished to access the data for any purpose.

IPD Sharing Access Criteria

Data requestors will need to contact renright@wisc.edu to gain access to the data. Data are available for 5 years at a third party website (Link to be included).

IPD Sharing Supporting Information Type

  • Study Protocol
  • Statistical Analysis Plan (SAP)
  • Informed Consent Form (ICF)
  • Clinical Study Report (CSR)
  • Analytic Code

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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