Evaluating the Hope@School Prevention Program
ConditionMental Health Wellness 1
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age8-18
SponsorKarolinska Institutet
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age between 8 and 18 years
Attends school included in the study
Consents to participate
Disqualifiers
None
Trial design
Design model
Parallel
Treatments tested in this trial
Hope@School
Other interventionA digital platform aimed at promoting student mental health in schools
Treatment as usual
Other interventionRegular student health care in schools
Treatment groups
3,220 Participants
are divided into 2 treatment groupsGroup A: Hope@SchoolExperimental treatment 1 intervention
Group B: Treatment as usualActive comparator 1 intervention
Trial outcomes
Primary outcomes
1
KIDSCREEN-27 Child version
Level of child-rated quality of life as measured by a questionnaire
Time frame
Baseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)Secondary outcomes
1
KIDSCREEN-27 Parent version
Level of parent-rated quality of life (the child's quality of life) as measured by a questionnaire
Time frame
Baseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)2
Mental Health-Promoting Knowledge (MHPK-10)
Level of child-rated mental health literacy as measured by a questionnaire
Time frame
Baseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)3
Healthy Behaviours in School-aged Children survey protocol (HBSC) part 1
Level of child-rated healthy behaviours as measured by a questionnaire
Time frame
Baseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)4
Digital Addiction Scale for Children (DASC)
Level of child-rated addictive digital behaviours as measured by a questionnaire
Time frame
Baseline, 3 month and 6 month (the 6 month assessment is the primary endpoint)Locations
Sponsors and contacts
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Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: