Reducing School Dropout and Enhancing Pupils' Sense of Belonging and Participation Through Co-created Music-based Activities (RESONATE)

June 2, 2026 updated by: Christian Gold, NORCE Norwegian Research Centre AS

Reducing School Dropout and Enhancing Pupils' Sense of Belonging and Participation Through Co-created Music-based Activities: The RESONATE Cluster-randomised Crossover Trial

RESONATE is a cluster-randomised crossover trial focusing on reducing school dropout rates and fostering belonging through co-created music-based activites, by combining music therapy (MT), psychology, and social sciences.

About 200 participants will be recruited in the area of Bergen, Norway. They will be randomized into the following intervention arms: group music activity followed by usual school schedule or usual school schedule followed by group music activity.

Study Overview

Detailed Description

RESONATE is a research initiative with researchers from Norway, Finland, and Denmark, and cultural organizations, the project employs an interdisciplinary approach combining music therapy, psychology, and social sciences. By engaging pupils, teachers, and community stakeholders, RESONATE develops and implements music interventions that promote emotional well-being, social inclusion, and resilience. These interventions align with Norway's current national school curriculum (LK20) and are informed by evidence-based research, including studies from WHO and music therapy scholars. Activities such as music-making and listening enhance social interaction, self-expression, and emotional support-key factors in reducing dropout risks.

The project follows a co-creation process, ensuring that interventions are designed with direct input from pupils and educators. A mixed-methods research approach, evaluates the impact of music activities on pupil engagement and well-being. Findings will be shared with policymakers, educators, the school sector, and welfare services to develop a transferable model applicable to schools nationally and internationally.

Study Type

Interventional

Enrollment (Estimated)

200

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Borre, Norway, 3199
    • Vestland
      • Bergen, Vestland, Norway, 5004
      • Bergen, Vestland, Norway, 5004
        • NAV Vestland
        • Contact:
      • Bergen, Vestland, Norway, 5009
        • Hyssingen Produksjonsskole
        • Contact:
      • Bergen, Vestland, Norway, 5010
      • Bergen, Vestland, Norway, 5011
      • Bergen, Vestland, Norway, 5015
        • Amalie Skram videregående skole
        • Contact:
      • Bergen, Vestland, Norway, 5015
      • Bergen, Vestland, Norway, 5020
        • Vestland Fylkeskommune Opplæring og Kompetanse
        • Contact:
      • Bergen, Vestland, Norway, 5824
      • Bergen, Vestland, Norway, 5832
      • Bergen, Vestland, Norway, 5857
      • Fyllingsdalen, Vestland, Norway, 5143
        • Fyllingsdalen videregående skole
        • Contact:
      • Isdalstø, Vestland, Norway, 5916
        • Knarvik videregående skole
        • Contact:
      • Olsvik, Vestland, Norway, 5183
        • Olsvikåsen videregående skole
        • Contact:
      • Straume, Vestland, Norway, 5353
        • Sotra videregående skole
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Pupils from the area Bergen, Norway.
  • High school pupils.
  • Sufficient Scandinavian language skills.
  • Between age 15-25.

Exclusion Criteria:

  • Does not speak a Scandinavian language sufficiently.
  • Planning to change school during the school year.
  • Uncorrected hearing impairment.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group music activity plus usual school schedule followed by usual school schedule alone
Group music activity is a music therapy intervention where participants will performe activites such as songwriting, music production and singing. The sessions will be conducted by an appropriately qualified music therapist, with support from the teacher and the researcher.
The participants will at first only attend a ordinary school schedule over 1 semester without group music activity. The next semester the participants will be followed by group music activity plus orinary school schedule.
Experimental: Usual school schedule alone followed by group music activity plus usual school schedule
Group music activity is a music therapy intervention where participants will performe activites such as songwriting, music production and singing. The sessions will be conducted by an appropriately qualified music therapist, with support from the teacher and the researcher.
The participants will at first only attend a ordinary school schedule over 1 semester without group music activity. The next semester the participants will be followed by group music activity plus orinary school schedule.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Absence from school (any reason)
Time Frame: 4 months, 10 months
Days of absence from school for any reason per semester, from school records
4 months, 10 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Absence from school (unexcused)
Time Frame: 4 months, 10 months
Days of unexcused absence from school per semester, from school records
4 months, 10 months
Healthy Use of Music Scale (HUMS Healthy)
Time Frame: 0 months, 4 months, 6 months, 10 months
Self-reported healthy music use. The scale consists of 5 items, each scored 1-5, to produce a total sum score from 5-25. Higher scores indicate more favourable use of music.
0 months, 4 months, 6 months, 10 months
Generalised Resistance Resources in School Scale (GRRS)
Time Frame: 0 months, 4 months, 6 months, 10 months
Self-reported generalised resistance resources in school. The scale consists of 9 items, each scored 1-5, to produce a total sum score from 9-45. Higher scores indicate a more favourable outcome (high degree of generalised resistance resources). Additionally there are 3 subscales (relational quality; task mastery in school; school motivation).
0 months, 4 months, 6 months, 10 months
Warwick-Edinburgh Mental Well-being Scale (WEMWBS)
Time Frame: 0 months, 4 months, 6 months, 10 months
Self-reported well-being. The scale consists of 14 items, each scored 1-5, summed to to produce a global score from 14-70. Higher scores indicate better mental well-being.
0 months, 4 months, 6 months, 10 months
Academic engagement (subscale of Positive Youth Development, PYD)
Time Frame: 0 months, 4 months, 6 months, 10 months
Self-reported academic engagement. The scale consists of 5 items, each scored 1-5. Mean scores are estimated. Score from 1-5. Higher scores indicate higher levels of academic engagement.
0 months, 4 months, 6 months, 10 months
Positive values (subscale of Positive Youth Development, PYD)
Time Frame: 0 months, 4 months, 6 months, 10 months
Self-reported positive values. The scale consists of 10 items, each scored 1-5. Mean scores are estimated. Score from 1-5. Higher scores indicate higher levels of positive values.
0 months, 4 months, 6 months, 10 months
Social competencies (subscale of Positive Youth Development, PYD)
Time Frame: 0 months, 4 months, 6 months, 10 months
Self-reported social competencies. The scale consists of 8 items, each scored 1-5. Mean scores are estimated. Score from 1-5. Higher scores indicate higher levels of social competencies.
0 months, 4 months, 6 months, 10 months
UCLA Loneliness Scale, short version
Time Frame: 0 months, 4 months, 6 months, 10 months
Self-reported loneliness. The scale consists of 3 items, each scored 1-3, to produce a total sum score from 3-9. Higher scores indicate less favourable outcomes (greater loneliness).
0 months, 4 months, 6 months, 10 months
Adverse events
Time Frame: 4 months, 10 months
Serious or non-serious, related or unrelated to study activities; reported by teachers
4 months, 10 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

August 15, 2026

Primary Completion (Estimated)

December 23, 2027

Study Completion (Estimated)

December 23, 2027

Study Registration Dates

First Submitted

June 2, 2026

First Submitted That Met QC Criteria

June 2, 2026

First Posted (Actual)

June 8, 2026

Study Record Updates

Last Update Posted (Actual)

June 8, 2026

Last Update Submitted That Met QC Criteria

June 2, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • RESONATE
  • ES747784 (Other Grant/Funding Number: Research Council of Norway)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-identified curated data will be made available permanently in publicly accessible repositories (e.g. OSF.io) using FAIR principles (e.g. using digital object identifiers [DOIs]; open, non-proprietary data formats; clear, consistent meta-data, using international standards for data structure where available; and licensed for re-use through CC BY). To balance the needs of trial participants for protection of their sensitive health data (in accordance with informed consent) and the needs of the scientific community for data availability, we will follow the principle "as closed as necessary, as open as possible". Results summaries will also be posted at Clinicaltrials.gov after the project end.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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