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NCT Number: NCT07401030

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

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.

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Key information

Age range

10 year–12 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Alpaslan Middle School

Ağrı, 25080, Turkey (Türkiye)

Location contact

YUSUF AKTEPE, MSc / Graduate Student / RN

CONTACT

aktepe.yusuf.akteğ[email protected]

+905439436504

YUSUF AKTEPE, MSc / RN / Graduate Student

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Psychological Resilience Training Program

Behavioral

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 utilization, and media use awareness and self-control.

Primary outcomes

  1. PSYCHOLOGICAL RESILIENCE

    Time frame: Time Frame: Baseline (before the intervention) and follow-up (one month after completion of the training program)

    Psychological resilience will be measured using the Children and Youth Resilience Measure-12 (CYRM-12). This scale assesses children's ability to cope with stress and challenging life situations. Total scores range from 12 to 60, with higher scores indicating greater psychological resilience.

Secondary outcomes

  1. SOCIAL ADJUSTMENT

    Time frame: Time Frame: Baseline (before the intervention) and follow-up (one month after completion of the training program)

    Social adjustment will be measured using the Social Adjustment Scale (SUÖ). This scale assesses children's ability to adapt to social rules, interact effectively with peers, and function appropriately in social settings. Total scores range from 55 to 275, with higher scores indicating better social adjustment.

  2. PROBLEMATIC MEDIA USE

    Time frame: Time Frame: Baseline (before the intervention) and follow-up (one month after completion of the training program)

    Problematic media use will be assessed using the Problematic Media Use Scale (PMKÖ), a parent-reported measure that evaluates children's difficulties in controlling and regulating digital media and screen use. Scores are calculated on a Likert-type scale ranging from 1 to 5, with higher scores indicating more problematic media use.

  3. PARENT-CHILD RELATIONSHIP

    Time frame: Time Frame: Baseline (before the intervention) and follow-up (one month after completion of the training program)

    Parent-child relationship will be assessed using the Parent-Child Relationship Scale (EÇİÖ), a parent-reported instrument consisting of 15 items that assess both positive and negative dimensions of the parent-child relationship. Items are rated on a 5-point Likert scale ranging from 1 (not at all) to 5 (extremely). Higher scores on the positive subscale indicate more positive relationship characteristics, whereas higher scores on the negative subscale indicate more negative relationship characteristics.

Study contacts

Contact information is provided by the study sponsor or research team.

YUSUF AKTEPE, MSc / Graduate Student

CONTACT

[email protected]

+905439436504

Sponsors and collaborators

Lead sponsor

Yusuf AKTEPE

Other

Registry information

Official study 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

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Feb 10, 2026
Registry last updated
Feb 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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