- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05234073
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
Status
Recruiting
Conditions
Intervention / Treatment
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
- Name: Eliza Kozasa, PhD
- Phone Number: +5511-2151-3354
- Email: elisa.harumi@einstein.br
Study Locations
-
-
-
Sao Paulo, Brazil, 05652901
- Recruiting
- Hospital Israelita Albert Einstein
-
Contact:
- Elisa H Kozasa, PhD
- Phone Number: 551121513747
- Email: elisa.harumi@einstein.br
-
São Paulo, Brazil, 05652901
- Recruiting
- Hospital Israelita Albert Einstein
-
Contact:
- Elisa Harumi Kozasa, PhD
- Phone Number: 551121513747
- Email: elisa.harumi@einstein.br
-
-
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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