School lessons in emotional skills may shield teens from mental health struggles
NCT ID NCT07796867
First seen Sep 01, 2026 · Last updated Sep 04, 2026 · Updated 2 times
Summary
This trial tests a school-based program called HENKA, designed to promote emotional well-being and prevent mental health problems in adolescents aged 12 to 16. The program includes eight classroom sessions on skills like self-esteem, emotional regulation, and mindfulness, taught by trained teachers with support from health professionals. Researchers will compare students in schools using the program with those in control schools, measuring changes in resilience among teens, their families, and school staff. The goal is to see if building resilience can help prevent mental health issues in young people.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Henka program, a school-based behavioral intervention with classroom sessions on emotional skills, delivered by trained teachers and supported by health professionals
- What this could lead to
- If effective, the program could offer schools a practical way to boost teen resilience and reduce the onset of mental health issues.
- What could go wrong
- The trial is not randomized, so results may be influenced by differences between schools. The program's success depends on teacher training and consistent delivery, which may vary.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 1,084 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2024
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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11 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Enrolled in Compulsory Secondary Education (ESO) in Catalonia, Spain. * Adolescents enrolled in 1st, 2nd or 3rd year of ESO. * Adolescents under 18 provide assent to participate; parents/guardians provide written informed consent. * Parents/guardians and teachers who sign informed consent participate in the program evaluation. Exclusion Criteria: * Parents/guardians who do not sign informed consent for minors under 18. * Adolescents who do not assent to participate. * Parents/guardians who do not sign their own informed consent. * Teachers who do not sign their informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Hospital Sant Joan de Déu Barcelona / Institut de Recerca Sant Joan de Déu
Esplugues de Llobregat, Barcelona, 08950, Spain
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