Clinical trial Recruiting at 4 sites Interventional Ages 9 to 15

Back2School: a Norwegian intervention to boost student attendance

Official title: Optimization and Testing Effectiveness of a Collaborative Intervention for School Attendance Problems in Norwegian Municipalities

Run by Norwegian University of Science and Technology · NCT07463001 · Data updated 2026-11-12

The study tests whether the Back2School program helps 9–15‑year-olds with low attendance in Norway, by starting the program now for half the participants and after 13 weeks for the other half, with both groups following the same school-supported plan.

Quick facts

Study typeInterventional
Ages9 Years to 15 Years
SexAll
Enrollment240 (estimated)
SponsorNorwegian University of Science and Technology
Academic / other
Locations4 sites (Bergen and 3 other locations)
StatusRecruiting
StartedApril 10, 2026
Main results expectedDecember 31, 2028
Study endsMarch 1, 2029
Registry record updatedOctober 15, 2026
Trial IDNCT07463001 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Children and adolescents aged 9–15 years with less than 80% school attendance in the past 12 weeks, with at least one Norwegian‑speaking parent willing to participate, and where the school agrees to participate.

Probably not a fit

Participants whose attendance issues are driven by factors outside the program scope or who require acute psychiatric intervention may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This randomized study adapts the Back2School program for Norwegian conditions to help students with ongoing attendance problems. Eligible participants are 9 to 15 years old with less than 80% attendance in the prior 12 weeks and at least one Norwegian-speaking parent who is willing to participate. After consent, eligibility screening, and randomization, the intervention begins with a school‑based assessment and a collaboratively developed plan, followed by 13 weeks of joint work among the youth, family, and school via a municipal team. Assessments occur after the 13‑week program and again at 6 months to measure attendance outcomes. All participants receive the intervention, with the control group delayed by 13 weeks to allow comparison of immediate versus delayed start.

Why it matters

Potential benefit: If successful, the program could improve school attendance and related outcomes for students with attendance problems.

How similar studies have gone: Previous similar approaches using collaborative, school‑based interventions have shown promise, though this Norwegian adaptation is novel in its specific delivery model and setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Participants must be between the ages of 9 and 15 at the time of enrollment.
2. Participants must have less than 80% attendance for the last 12 weeks of school at the time of screening.
3. At least one parent has to talk and understand Norwegian.
4. At least one parent has to be motivated to participate.
5. The school must agree to participate in the intervention

Exclusion Criteria:

1 The participant has a known diagnosis of autism-spectrum disorder, psychosis, and/or eating disorder.

2\. Participant needs acute psychiatric intervention.

Where it's running

  • NORCE, RKBU Vest
    Bergen, Norway
    Recruiting
  • Pilar, Regionsenter for barn og unges psykiske helse
    Oslo, Norway
    Recruiting
  • UIT, RKBU Nord
    Tromsø, Norway
    Recruiting
  • Norwegian University of Scinece and Technology
    Trondheim, Norway
    Recruiting

Study contacts

  • Principal investigator: Jo Magne Ingul, phd — Norwegian University of Science and Technology
  • Study coordinator: Jo M Ingul, phd
  • Email: jo.m.ingul@ntnu.no
  • Phone: +4792869163

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.