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Echo: Optimizing a Group-based School Intervention for Children With Emotional Problems

Echo: Optimizing a Group-based School Intervention for Children With Emotional Problems

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04263558
Enrollment
1364
Registered
2020-02-11
Start date
2020-02-13
Completion date
2023-05-25
Last updated
2023-11-29

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

Conditions

Anxiety Depression

Brief summary

The present study (Echo) will promote much needed research and innovation that optimize service provision in first line health services for the alarmingly high number of school children who suffer from clinical and subthreshold levels of anxiety and depression. The effect of different versions of an evidence-based intervention for this group of children will be tested using a cluster randomized design involving 40 schools across Norway. The aim is to create a framework that allows more evidence-based psychosocial interventions to be provided at a lower cost to society. Echo will provide knowledge about three main evidence gaps for children: (1) The effect of school-based preventive interventions on anxiety and depression; (2) The effect of feedback informed systems, and; (3) the effect and cost-effectiveness of digital health interventions using online sessions and virtual reality technology.

Interventions

BEHAVIORALEmotion child

The MFS will include an idiographic measure of personal aims, symptom burden, displayed on a visual data dashboard to guide further intervention. The EMOTION intervention for children 9 to 12 years with symptoms of anxiety and/or depression will be used in a standard/long version (16 sessions) and a short (8 sessions) but optimized version, using a partial web-based solution with virtual reality (VR)-technology for behavioral experiments and exposure (in short and long version). Parental involvement: Parental participation in a 5-session parent group (high involvement) versus sharing information with parents via a brochure (low Parental involvement).

Sponsors

University of Tromso
CollaboratorOTHER
Technical University of Trondheim
CollaboratorUNKNOWN
Regionsenter for barn og unges psykiske helse
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

The study will have a stratified, randomized cluster design. The schools are clusters randomized to different experimental conditions. The factors are (1) feedback from a MFS-system, yes/no, (2) Evidence Based Intervention, long/short (EBI), and (3) parental involvement, high/low. The three factors are related components that, together, should form the strongest intervention outcomes. Each of the 40 recruited schools will therefore be randomly assigned to one of eight experimental conditions

Eligibility

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

Inclusion criteria

• Children scoring one standard deviation or more above population mean using established measures for anxiety and/or depression

Exclusion criteria

* Retardation or language problems * Developmental conditions * Individual considerations approved by the local PI

Design outcomes

Primary

MeasureTime frameDescription
Multidimensional Anxiety ScaleTime 1 baselineAnxiety symptoms, minimum 0 to maximum 117, high score indicates worse outcome
Mood and Feeling QuestionnaireTime 1 baselineDepression symptoms, minimum 0 to maximum 26, high score indicates worse outcome

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026