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Effectiveness of Enhanced Mental Health Support for Young People

Effectiveness of Enhanced Mental Health Support for Young People

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05356949
Acronym
Nopsatuki
Enrollment
124
Registered
2022-05-02
Start date
2020-01-01
Completion date
2023-12-31
Last updated
2023-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety, Depression, Emotional Stress

Keywords

Depression, Anxiety, Intervention, Adolescents, School

Brief summary

The aim of the research project is to measure the effectiveness of an early and rapid psychiatric nurse intervention at schools in improving the emotional well-being and functioning of adolescents.

Detailed description

In this study, the impact of a short psychological intervention on adolescent emotional well-being, symptoms, and functioning is assessed. The intervention is a short intervention based on the methods of cognitive-behavioral therapy comprising 6 weekly sessions. It is delivered by psychiatric nurses working in the schools in the City of Turku. The participants are adolescents aged 12-18 who seek student health care due to mental health problems. The goal is to recruit 150 participants. The intervention is not tied to some particular disorder and thus, the main response variable is emotional well-being. Emotional well-being is measured at both the beginning and the end of the intervention, and at 6-month follow-up using the Young Person's Clinical Outcomes for Routine Evaluation (YP-CORE) questionnaire. Effectiveness is measured as a change in the YP-CORE scores.

Interventions

BEHAVIORALIntervention

The participants receive a psychological intervention including six weekly sessions. The intervention is based on methods of cognitive-behavioral therapy and delivered by a psychiatric nurse working in the participant's school.

Sponsors

University of Turku
CollaboratorOTHER
City of Turku
CollaboratorOTHER_GOV
Turku University Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Young Person's Clinical Outcomes for Routine Evaluation (YP-CORE) score ≥14 * Willing and able to commit to the intervention and study protocol * Sufficient proficiency in Finnish

Exclusion criteria

* Other ongoing mental health treatment * Substance use as the main problem

Design outcomes

Primary

MeasureTime frameDescription
Emotional well-being, short-term6 weeksChange from the baseline to the end of the intervention in the Young Person's Clinical Outcomes for Routine Evaluation (YP-CORE) score. The score range for the scale is 0-40 and lower scores indicate better emotional well-being.

Secondary

MeasureTime frameDescription
Emotional well-being, long-term6 monthsChange from the baseline to the 6 month follow-up time-point in the Young Person's Clinical Outcomes for Routine Evaluation (YP-CORE) score. The score range for the scale is 0-40 and lower scores indicate better emotional well-being.

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 10, 2026