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Evaluating the Hope@School Prevention Program

Feasibility, Effectiveness and Overall Impact of the Hope@School Universal Prevention Program Promoting Child and Adolescent Mental Health in Schools: A Two-arm Randomized Controlled Trial Across Seven European Countries

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06359262
Acronym
Hope@School
Enrollment
3220
Registered
2024-04-11
Start date
2027-01-01
Completion date
2028-12-30
Last updated
2024-04-11

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

Conditions

Mental Health Wellness 1

Brief summary

This multi-center cluster-randomized controlled trial aims to evaluate the feasibility, effectiveness and overall impact of the Hope@School (H@S) program by comparing mental health outcomes in students participating in the H@S program with students having only access to regular student health care (treatment as usual - TAU). The primary objectives of the study are: To determine if the H@S program is feasible, acceptable, usable and safe for students, families, teachers and school leaders To establish if the H@S program is associated with improvements in quality of life, everyday functioning, peer relations and general mental health.

Interventions

OTHERHope@School

A digital platform aimed at promoting student mental health in schools

OTHERTreatment as usual

Regular student health care in schools

Sponsors

Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
8 Years to 18 Years
Healthy volunteers
Yes

Inclusion criteria

* Age between 8 and 18 years * Attends school included in the study * Consents to participate

Exclusion criteria

\- Younger than 8 and older than 18 years

Design outcomes

Primary

MeasureTime frameDescription
KIDSCREEN-27 Child versionBaseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)Level of child-rated quality of life as measured by a questionnaire

Secondary

MeasureTime frameDescription
KIDSCREEN-27 Parent versionBaseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)Level of parent-rated quality of life (the child's quality of life) as measured by a questionnaire
Mental Health-Promoting Knowledge (MHPK-10)Baseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)Level of child-rated mental health literacy as measured by a questionnaire
Healthy Behaviours in School-aged Children survey protocol (HBSC) part 1Baseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)Level of child-rated healthy behaviours as measured by a questionnaire
Digital Addiction Scale for Children (DASC)Baseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)Level of child-rated addictive digital behaviours as measured by a questionnaire
Healthy Behaviours in School-aged Children survey protocol (HBSC) part 2Baseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)Level of child-rated harmful digital practices as measured by a questionnaire

Contacts

Primary ContactJens Högström, Ass. prof
jens.hogstrom@ki.se0046 70 9689161

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026