Be-Prox. An Effectiveness Study of Bullying Intervention in Norwegian Kindergartens. (NCT06040437) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Be-Prox. An Effectiveness Study of Bullying Intervention in Norwegian Kindergartens.
Norway2,500 participantsStarted 2023-08-07
Plain-language summary
With an overall aim to ensure a safe and sound kindergarten environment for all Norwegian children in accordance with the Kindergarten Act §§41-43, the objectives of the current project are:
To evaluate the effectiveness of Be-Prox Norway to prevent and handle negative behavior and bullying among peers in Norwegian kindergartens.
To examine implementation factors that promote and inhibit the effectiveness of Be-Prox Norway in Norwegian kindergartens.
To describe the cost-effectiveness of the Be-Prox Norway intervention in Norwegian kindergartens.
To generate knowledge on how the Be-Prox Norway intervention can be aligned and implemented in Norwegian kindergartens.
Who can participate
Age range
3 Years – 6 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 born 2018-2020 in kindergartens enrolled to the Be-Prox project and with parental consent to participate.
* Personnel i Norwegian kindergartens enrolled in the Be-Prox project and who consent to participate.
* Parents of children in kindergartens enrolled to the Be-prox project
Exclusion Criteria:
* children born 2021-2023
* children with no parental consent to participate
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
Total number of negative acts children have been exposed to by peers the last months post intervention.
Timeframe: Scorers are asked to use "the last 4 weeks" as the time frame for their registration of the negative acts
2
Total number of negative acts children have exposed peers to the last month post intervention.
Timeframe: Scorers are asked to use "the last 4 weeks" as the time frame for their registration of the negative acts