Clinical trial Recruiting at 2 sites Interventional Ages 5 to 18

Nature- and activity-based group programs for neurodivergent children and youth in Agder

Official title: Where Wild Things Grow: Immediate and Long-term Impact of Nature- and Activity-based Group Interventions for Neurodivergent Children and Youth in School, Health Care and Leisure Settings in Agder

Run by Sorlandet Hospital HF · NCT07203469 · Data updated 2026-11-12

This project will try outdoor and activity-based group programs to see if they help children and teens with ADHD, autism, Tourette's, and related neurodivergent challenges feel better, gain confidence, and do better in daily life.

Quick facts

Study typeInterventional
Ages5 Years to 18 Years
SexAll
Enrollment240 (estimated)
SponsorSorlandet Hospital HF
Government
Locations2 sites (Kristiansand, Agder and 1 other locations)
StatusRecruiting
StartedSeptember 1, 2025
Main results expectedJune 15, 2026
Study endsJune 15, 2027
Registry record updatedOctober 2, 2025
Trial IDNCT07203469 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Children and adolescents in the Agder region who are neurodivergent (for example ADHD, autism, or Tourette's) or whole classes that include such students and who can participate in group outdoor activities are the intended participants.

Probably not a fit

Patients with active substance misuse, acute psychosis, current suicidal ideation, severe eating disorders, or those unable to take part in outdoor group activities are unlikely to benefit or be eligible.

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

What this trial studies

This action research project develops and implements nature- and activity-based group interventions across healthcare, school, and community settings in the Agder region of Southern Norway. Interventions use universal and selective approaches and include outdoor therapy and climbing activities tailored to support mental health, self-efficacy, and daily functioning in neurodivergent children and youth. Outcomes include measures of quality of life, self-efficacy, self-esteem, and physiological reactions, with comparisons between nature-based and traditional indoor provision. Recruitment occurs at class-level for school-based arms and at the patient level for healthcare interventions, with standard exclusions for acute severe mental-health conditions.

Why it matters

Potential benefit: If successful, these programs could provide accessible, non-medical ways to improve quality of life, self-confidence, and everyday functioning for neurodivergent children and adolescents.

How similar studies have gone: Smaller studies and program evaluations of nature-based interventions have shown promising mental health and well-being effects in young people and some neurodivergent groups, but large controlled trials are still limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* In PhD 1, participants are recruited on class-level (all) or individual (identified need).
* In PhD 2, inclusion criteria are patients that participate in the specific interventions.

Exclusion Criteria:

* In PhD 2, exclusion criteria include substance misuse, acute psychosis, current suicidal behavior/ideation, and severe eating disorders.

Where it's running

  • Department of Child and Adolescent Mental Health (ABUP), Sørlandet Hospital HF
    Kristiansand, Agder, Norway
    Recruiting
  • Department of Sport and Physical Education, University of Agder
    Kristiansand, Agder, Norway
    Recruiting

Study contacts

  • Principal investigator: Carina R Fernee, PhD — Sørlandet Hospital HF
  • Study coordinator: Carina R Fernee, PhD
  • Email: carina.fernee@sshf.no
  • Phone: +4790671621

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.