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Not yet recruiting NCT07401030

Effectiveness of a Psychological Resilience Training Program for Children Aged 10-12

No phase Interventional Psychological Resilience Social Adjustment Interpersonal Relationships Media Use

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Psychological Resilience Training Program.
Who it may be relevant to
Registry conditions: Psychological Resilience, Social Adjustment, Interpersonal Relationships, Media Use. Basic parameters: 10 years — 12 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effectiveness of a Psychological Resilience Training Program for Children Aged 10-12: An Evaluation in Terms of Psychological Resilience, Social Adjustment, Close Relationships, and Media Use

Overview

This clinical study aims to learn whether a psychological resilience training program is helpful for children aged 10 to 12 years. The program is designed to help children cope better with stress, get along better with others, and use digital media in a healthier way. The main questions this study seeks to answer are: Does the training increase children's psychological resilience? Does it improve children's social adjustment and close relationships with family and friends? Does it help reduce problematic media use? Children who take part in the study are randomly assigned to one of two groups. One group takes part in a psychological resilience training program, and the other group does not receive any training during the study period. Children and their parents complete questionnaires before the program and again after the program is completed.

Detailed description

This study is planned as a randomized controlled interventional trial to evaluate the effects of a structured psychological resilience training program on multiple psychosocial outcomes in children aged 10-12 years. The study will be conducted in a school setting in Agri, Turkey.

A total of 50 eligible children who meet the inclusion criteria will be enrolled in the study. After completion of baseline assessments, participants will be randomly assigned to an intervention group (n = 25) or a control group (n = 25) using a simple randomization method. Group allocation will be coded to reduce potential bias during data analysis. Participants and their parents will not be informed about group assignment, and statistical analyses will be performed by an independent analyst who will be blinded to group codes.

The intervention group will receive a school-based psychological resilience training program developed for children and adolescents. The program will be delivered in a group format and will consist of 10 sessions implemented over a five-week period, with two sessions per week. The session content will include emotional awareness and regulation, self-awareness and identification of personal strengths, self-efficacy, coping with stressful situations, problem-solving skills, cognitive flexibility, social skills development, communication skills, utilization of social support resources, and media use awareness and self-control. The control group will not receive any intervention during the study period and will participate only in assessment procedures.

Data will be collected at two time points: at baseline (prior to randomization) and at follow-up after completion of the intervention period. Child-reported and parent-reported standardized measures will be used to assess psychological resilience, social adjustment, problematic media use, and parent-child relationship characteristics. The study will be conducted in accordance with ethical principles and will be approved by a university ethics committee prior to participant enrolment.

Interventions

  • Behavioral Psychological Resilience Training Program
    This is a structured, school-based psychological resilience training program designed for children aged 10-12 years. The program consists of 10 group sessions delivered over a five-week period (two sessions per week). Session content includes emotion recognition and regulation, self-awareness and identification of personal strengths, self-efficacy, coping with stressful situations, problem-solving skills, cognitive flexibility, social skills development, communication skills, social support util

Primary outcome measures

  • PSYCHOLOGICAL RESILIENCE [Time frame: Time Frame: Baseline (before the intervention) and follow-up (one month after completion of the training program)]
Secondary outcome measures (3)
  • SOCIAL ADJUSTMENT [Time frame: Time Frame: Baseline (before the intervention) and follow-up (one month after completion of the training program)]
  • PROBLEMATIC MEDIA USE [Time frame: Time Frame: Baseline (before the intervention) and follow-up (one month after completion of the training program)]
  • PARENT-CHILD RELATIONSHIP [Time frame: Time Frame: Baseline (before the intervention) and follow-up (one month after completion of the training program)]

Eligibility criteria

Inclusion criteria

  • Children aged 10 to 12 years
  • Enrollment in a primary or middle school
  • Ability to understand and participate in group-based educational activities
  • Willingness of the child to participate in the study
  • Written informed consent provided by a parent or legal guardian
  • No prior participation in a psychological resilience or emotional regulation training program

Exclusion criteria

  • Presence of a diagnosed severe psychiatric disorder (e.g., psychotic disorders or severe behavioral disorders)
  • Cognitive impairment that would prevent understanding the training content or completing assessments
  • Participation in another psychological or behavioral intervention during the study period
  • Absence from a substantial portion of the intervention sessions
  • Withdrawal of consent by the child or parent/legal guardian at any stage of the study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Health services research

Study locations

Turkey (Türkiye) · 1 center
  • Alpaslan Middle School — Ağrı

Publications

  • Masten AS. Resilience in children threatened by extreme adversity: frameworks for research, practice, and translational synergy. Dev Psychopathol. 2011 May;23(2):493-506. doi: 10.1017/S0954579411000198. PMID 23786691

Identifiers

NCT: NCT07401030 · AICU-SBF-YA-01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗