Effects of a Four Weeks Social Emotional and Ethical Learning Training in Brazilian Public School Teachers

October 13, 2022 updated by: Hospital Israelita Albert Einstein

Effects of a Four Weeks Social Emotional and Ethical Learning Training in Brazilian Public School Teachers: a Randomized Controlled Trial

Social Emotional Learning (SEL) has gained importance in recent years and has been taught in several schools to support students in how to recognize and manage emotions, develop empathy, build cooperative relationships, solve problems effectively, and gain skills of communication. The objective of this study is to evaluate the effects of a training of 4-week Social Emotional and Ethical Learning on stress, well-being, socioemotional learning literacy, positive and negative affect, attention, and competent. This study will also assess the perception of teachers about training and its impact on their teaching skills and in personal life. Methods: Elementary and Secondary School Teachers public in Brazil (N = 1,500) will be invited to participate in the SEE training Learning. After signing the Free and Informed Consent Term, the they will be randomized into two groups A and B. Both groups will be before the experiment (T0), after one month (T1) and after two months (T2). ONE SEE Learning Training (SEELT) and B will be a checklist control group. Standby (WLC) for one month. After that, B will receive SEELT and A will not receive intervention, but will be guided to maintain the practices learned. RESULTS EXPECTED: The groups after receiving the SEELT should present better results relating to their socio-emotional skills, stress management, increase in well-being and knowledge about these skills, are still so, better prepared to teach their students.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

1500

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 Locations

      • Sao Paulo, Brazil, 05652901
        • Recruiting
        • Hospital Israelita Albert Einstein
        • Contact:
      • São Paulo, Brazil, 05652901
        • Recruiting
        • Hospital Israelita Albert Einstein
        • Contact:

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

18 years to 99 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Teachers from the public schools in Brazil

Exclusion Criteria:

-

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: Crossover Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Experimental: A (first group to receive the intervention)
The class will be instructed in the social emotional and ethical learning (SEELearning) for 4 weeks.
This intervention includes classes about socioemotional learning theory and practice, topics related to ethics and well-being practices
Experimental: Experimental: B (second group to receive the intervention)
This arm will not receive intervention in the first month and will receive SEE Learning after this period.
This intervention includes classes about socioemotional learning theory and practice, topics related to ethics and well-being practices
This group will wait for one month to receive SEE Learning Online Training

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in stress
Time Frame: 1 month

The authors will evaluate stress using the 10-item perceived stress scale. Higher values means worse stress.

2. change in attention The authors will apply the Perceived Stress Scale

1 month
Change in well-being perception
Time Frame: 1 month
The authors will evaluate well-being using the World Health Organization 5-item well-being index. Higher scores means better well-being.
1 month
Understanding of the application of socio-emotional and ethical learning
Time Frame: 1 month
Questionnaire on Knowledge about Socioemotional Learning and Ethics. This is a 0 to 10 score questionnaire. Higher scores means better understanding in the topic.
1 month

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Effectiveness of content learning and training appreciation
Time Frame: 1 month
Qualitative interviews in focus groups will be carried out among the participants
1 month
change in positive and negative affect (PANAS)
Time Frame: 1 month
The authors will apply Positive and Negative Affect Scale (PANAS). Higher scores in negative affect means worse affective state and higher scores in positive affect means better affective state.
1 month
Perception of Stress, Well-Being, Attention, Frustration, Motivation in the last week
Time Frame: 1 month
the author will aply "Questionary of Perception of Stress, Well-Being, Attention, Frustration, Motivation in the Last Week". Each item will be answered in a 0 to 10 item scale. The minimum value is 0 and the maximum is 10. Higher scores in stress and frustration are worse scores. Higher scores in well-being, attention and motivation are better scores in the questionnaire.
1 month

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)

March 1, 2022

Primary Completion (Anticipated)

December 1, 2022

Study Completion (Anticipated)

July 1, 2023

Study Registration Dates

First Submitted

February 1, 2022

First Submitted That Met QC Criteria

February 1, 2022

First Posted (Actual)

February 10, 2022

Study Record Updates

Last Update Posted (Actual)

October 14, 2022

Last Update Submitted That Met QC Criteria

October 13, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • HIAE_SEELT_BR

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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