Effectiveness of a Psychological Resilience Training Program for Children Aged 10-12 (NCT07401030) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effectiveness of a Psychological Resilience Training Program for Children Aged 10-12
Turkey (Türkiye)50 participantsStarted 2026-02-02
Plain-language summary
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.
Who can participate
Age range
10 Years – 12 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
PSYCHOLOGICAL RESILIENCE
Timeframe: Time Frame: Baseline (before the intervention) and follow-up (one month after completion of the training program)