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New study aims to stop youth mental health crises before they start

NCT ID NCT07413887

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests five programs designed to prevent serious mental health issues in young people. The programs include early screening, therapy, and support at school. Researchers will compare these programs to usual care in 1,200 teens aged 12-17. The goal is to see if early help can improve well-being and reduce problems like eating disorders, anxiety, and self-harm.

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

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

About 1,200 people

The number the study aims to enrol. It can still change while the study runs.

Started

Nov 2025

Expected to finish

Feb 2028

An estimate. End dates often move.

Lead sponsor

A research network

The lead sponsor is a research network or cooperative group.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

3 to 17 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show 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.

Each of the interventions has elaborate and narrowly defined inclusion and exclusion criteria. These are listed below for each intervention. 'Signs of Internalizing' Inclusion criteria * Adolescents aged 12-17 years * Mild to moderate impairment in daily functioning (e.g., reduced engagement in school, social life, or leisure activities compared to before symptoms) * Adolescents with well-managed ADHD or autism may be included if they demonstrate sufficient mentalizing abilities and can benefit from the intervention with parental support * Presence of both anxiety and depressive symptoms, neither of which dominates or meets full diagnostic criteria * The family is motivated to participate Exclusion criteria * Symptoms of moderate to severe depression * Presence of OCD, PTSD, agoraphobia, panic disorder, or other psychiatric conditions * Low cognitive functioning * Moderate to severe functional impairment (e.g., school dropout, extreme social withdrawal, daily reliance on adult support, lack of motivation for treatment) * Recent unsuccessful psychological treatment * Primary problems related to family dynamics or a highly burdened family situation * Increased or acute suicide risk * Presence of self-harm or symptoms of disordered eating 'Signs of Disordered Eating' Inclusion criteria * Children and adolescents aged 10-17 years * High body dissatisfaction, preoccupation with food and/or body image, and/or early behavioral signs of an eating disorder * Stable physical condition, manageable in consultation with the adolescent's general practitioner * Able to consume food with guidance and support * The family is motivated to participate Exclusion criteria * Previous treatment for an eating disorder * Symptoms meeting criteria for specialized psychiatric treatment * Low cognitive functioning * Significant weight loss * Solely restrictive or selective eating without other eating disorder symptoms * Severe comorbidity * Increased or acute suicide risk * Eating difficulties solely related to lifestyle factors 'Signs of Self-Harm' Inclusion criteria * Adolescents aged 12-17 years * Current thoughts of self-harm * At least one episode of direct (non-suicidal) self-harm within the past three months * The family is motivated to participate Exclusion criteria * Increased suicide risk * Psychiatric disorder requiring further assessment or not adequately treated * Low cognitive functioning * Self-harm only in socially accepted contexts (e.g., piercings or tattoos) * Only indirect self-harm (e.g., excessive substance use) * Only self-harm by proxy (involving another person) 'Take the Control Back' Inclusion criteria * Children and adolescents aged 5-17 years * Experiencing obsessive thoughts and/or compulsive behaviors of mild to moderate severity * Experiencing self-perceived distress related to obsessive thoughts and/or compulsive behaviors * Experiencing obsessive thoughts as egodystonic, and thus aware that they are excessive (for the youngest participants, this criterion may be waived in cases of limited insight) * Functioning is impaired by obsessive thoughts and/or behaviors, e.g., reduced school functioning, social difficulties, or impaired functioning at home * The family is motivated to participate Exclusion criteria * Symptoms meeting criteria for specialized psychiatric treatment * Has another psychiatric disorder that requires assessment or is not adequately managed * Has difficulties other than obsessive thoughts and behaviors that currently constitute the primary burden, and which must be addressed first * Has previously received OCD treatment within psychiatric care (may be offered STIME if assessed but not treated due to mild severity) * Has an increased or acute risk of suicide * Has low functioning for other reasons, e.g., significantly reduced cognitive functioning 'the Parent Pilots' Inclusion criteria * Parents of children aged 3-10 years who experience developmentally inappropriate difficulties with restlessness, hyperactivity, attention, and/or impulsivity * The symptoms must be present at home as a minimum, but may also occur across settings such as home, daycare, and school * The child's difficulties must be significant enough to affect overall daily functioning * The parents are motivated to participate Exclusion Criteria: * Symptoms of attention difficulties that require psychiatric treatment * Presence of another psychiatric disorder that requires treatment * Previous treatment for ADHD within the psychiatric system * Low level of functioning due to other causes, such as significantly reduced cognitive functioning

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Conditions

The condition(s) this trial relates to.

Psychological Well-Being

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

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  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Center for Clinical Research and Prevention

    RECRUITING

    Frederiksberg, Denmark

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