The Effects of Group Social Work Intervention on Children's Emotional Intelligence, Emotion Regulation Skills and Empathy Tendencies

December 5, 2025 updated by: merve özkul, Selcuk University

The Effect of Group Social Work Intervention Based on Emotion-Focused Therapy on Emotion Regulation Skills, Emotional Intelligence and Empathic Tendency Levels of Children in Need of Protection

The general objective of this study is to determine the effects of an emotion-focused therapy-based group social work intervention on the emotion regulation skills, emotional intelligence, and empathic tendency levels of children aged 9-11 years in need of protection and living in a children's home complex, and to explore the participants' experiences of the group intervention. The independent variable of the study is the emotion-focused therapy-based group social work intervention. The dependent variables are the children's emotion regulation skills, emotional intelligence, and empathic tendency levels.

Within the framework of the stated general objective, the quantitative questions addressed in the study are as follows:

  1. Is there a significant difference between the emotion regulation skills, emotional intelligence, and empathic tendency scores between the experimental and control groups before the intervention?
  2. Is there a significant difference between the pre-test and post-test scores of the emotion regulation skills, emotional intelligence, and empathic tendency of the participants in the experimental group after the intervention?
  3. After the intervention, is there a significant difference between the pre-test and post-test scores on emotion regulation skills, emotional intelligence, and empathic tendency of the participants in the control group?
  4. After the intervention, is there a significant difference between the post-test scores on emotion regulation skills, emotional intelligence, and empathic tendency of the participants in the experimental group and the post-test scores on emotion regulation skills, emotional intelligence, and empathic tendency of the participants in the control group?

Study Overview

Detailed Description

-Participants in the study completed the Children's Emotion Regulation Scale (CRS), the BarOn Emotional Intelligence Test Child and Adolescent Form and the KA-Si Empathic Tendency Scale Child Form before the study began. Following the 12-session group process, the same scales were completed for both the experimental and control groups, and differences between the experimental and control groups were examined.

Some participants had difficulty reading and understanding the scale items during the pretest and posttest evaluation processes. Both tests were administered one-on-one with the participants, and those who did not understand were read one by one. The quantitative data collected were then entered into SPSS.

Study Type

Interventional

Enrollment (Actual)

38

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

    • Pursaklar
      • Ankara, Pursaklar, Turkey (Türkiye)
        • Ankara Çocuk Evleri Sitesi Müdürlüğü

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

  • Child

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • • Be between 9 and 11 years old

    • Be able to read and write
    • Have no known traumatic event/abuse history
    • Have been accepted to the organization for at least 3 months (have adapted to the organization)
    • Have no severe/advanced psychiatric disability/diagnosis
    • Have been declared suitable by the group leader
    • Be willing to participate in the study

Exclusion Criteria:

  • • Being outside the 9-11 age range

    • Being admitted to the institution less than 3 months ago or not yet having adapted to the institution
    • Being a foreign national
    • Not knowing Turkish
    • Having a history of abuse
    • Being hospitalized
    • Being a child who left the institution without permission
    • Being in the final stages of transfer and return to family

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: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: emotion-focused group social work
The group where 12 sessions of emotion-focused group social work were conducted
Emotion-focused therapy, a therapy approach that prioritizes emotions over others, advocates for increasing emotional intelligence, which refers to using emotions as a developmental tool without being dominated by them (Greenberg, 2004b). Emotion-focused therapy, which places emotions at the center, is a practice that has recently become widespread in our country. It is stated that this approach helps individuals identify/be aware of their emotions, express them, make sense of them, appropriately modify/transform them, and use them in a healthy way; as a result, individuals are more successful in taking control of their lives (Greenberg 2010). From this perspective, it is believed that working with children in need of protection using this approach will be beneficial for the children themselves. The results of this study suggest that it may contribute to introducing an emotion-focused perspective into rehabilitative work with children under protection.
No Intervention: no emotion-focused group social work
no intervention group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
BarOn Emotional Intelligence Scale Child and Adolescent Form
Time Frame: up to 12 weeks after registration
This is a 60-item scale, with a minimum score of 60 and a maximum of 240. Higher scores indicate better outcomes, as they indicate improved emotional intelligence skills.
up to 12 weeks after registration
Emotion Regulation Scale for Children
Time Frame: up to 12 weeks after registration
The scale consists of 29 items and four subscales: anger (9 items), fear (8 items), sadness (7 items), and excitement (5 items). The lowest score is 29; the highest is 116. Higher scores indicate better outcomes.
up to 12 weeks after registration
KA-SI Empathic Tendency Scale - Child Form
Time Frame: up to 12 weeks after registration
The scale consists of 13 items. The minimum score is 13, and the maximum score is 52. As the scale scores increase, empathic tendency increases, and as they decrease, empathic tendency decreases.
up to 12 weeks after registration

Collaborators and Investigators

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

Investigators

  • Study Director: Serap D DAŞBAŞ, Prof. Dr., Selcuk University

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.

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 5, 2025

Primary Completion (Actual)

November 6, 2025

Study Completion (Estimated)

February 25, 2026

Study Registration Dates

First Submitted

November 22, 2025

First Submitted That Met QC Criteria

December 5, 2025

First Posted (Actual)

December 10, 2025

Study Record Updates

Last Update Posted (Actual)

December 10, 2025

Last Update Submitted That Met QC Criteria

December 5, 2025

Last Verified

December 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

I haven't decided yet

Study Data/Documents

  1. Clinical Study Report
    Information identifier: merve özkul/author

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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