Nature-based program feasibility in preschools near public housing
Official title: A Feasibility Study of a Cluster Randomized Controlled Trial of a Nature-based Intervention Enhancing Mental and Physical Well-being Among Kindergarten Children From Deprived Areas: Nurture by Nature
Run by University Hospital Bispebjerg and Frederiksberg · NCT07780123 · Data updated 2026-11-12
This feasibility study tests whether a nature-based program in preschools near public housing can be run smoothly and whether families will participate and benefit.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 4 Years and up |
| Sex | All |
| Enrollment | 127 (estimated) |
| Sponsor | University Hospital Bispebjerg and Frederiksberg Academic / other |
| Locations | 1 site (Frederiksberg) |
| Status | Recruiting |
| Started | October 1, 2026 |
| Main results expected | May 1, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | September 1, 2026 |
| Trial ID | NCT07780123 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal participants are children aged 4-7 years in preschools near social housing areas, with Danish-speaking parents who consent.
✕Probably not a fit
Children or families not aligned with the intervention or unable to participate in follow-up assessments 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 project is a feasibility cluster randomized trial to see if a future large pragmatic trial can test a nature-based intervention's effects on children's mental and physical health. It compares a 14-week nature-based program with usual preschool activities in similar settings, focusing on acceptability, recruitment, data collection, and safety. Outcomes include parent and child assessments, motor development, physical activity, sleep, absenteeism, and stress, with data also gathered from educators and parents. The study is conducted in preschools located in or near social housing areas and will measure feasibility metrics to inform a larger trial.
Why it matters
Potential benefit: If successful, the approach could support better mental and physical health for children through increased nature exposure in early childhood.
How similar studies have gone: There is emerging interest in nature-based interventions, with limited feasibility data in this specific setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: A kindergarten cluster will be eligible for study participation if the cluster meets the following criteria: 1. The kindergarten should geographically be located within or near by a social housing area or serve children from such an area. 2. At least 11 children in the cluster, each: 1. aged 4-7 years due to the primary outcome cutoff age, and 2. have a parent who is able to understand and communicate in Danish, and 3. have consented to participate Inclusion criteria of children and parents: A child and parent will be eligible for study participation if they meet the following criteria: 1. the child is aged 4-7 years due to the primary outcome cutoff age, and 2. the parent is able to understand and communicate in Danish, and 3. have consented to participate Inclusion criteria of kindergarten personnel: Kindergarten personnel will be eligible for study participation if they meet the following criteria: 1. if they have \>80% of their working hours in the eligible kindergarten cluster 2. have consented to participate Exclusion Criteria: A kindergarten cluster will not be eligible for the study if the cluster meets any of the following criteria: 1. the kindergarten is currently spending \> two days per week in nature (green outdoor), 2. the kindergarten is already using the ''Green Sprouts'' program, 3. the kindergarten is exclusively for children with special needs All exclusion criteria are at cluster level. There are no individual exclusion criteria.
Where it's running
-
Bispebjerg and Frederiksberg Hospital, The Parker Institute
Frederiksberg, Denmark Recruiting
Study contacts
- Study coordinator: Ina O Specht, PhD
- Email: ina.olmer.specht@regionh.dk
- Phone: 004538163083
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Relaxation audio during breastfeeding to help newborn growth and mom’s well-being
Researchers will test if listening to a relaxation audio during breastfeeding helps LBW babies grow and reduces maternal stress in a Ugandan setting.
-
Mindfulness-Based Stress Reduction Program for nursing students
This trial tests whether a Mindfulness-Based Stress Reduction program can help nursing students reduce stress and improve mood and well-being.
-
Moving Kindergartens: Supporting daily movement and joy for preschool children
This project will try a 10-week program co-designed with kindergarten staff to increase daily movement, motor skills, and well-being among preschool children and see if the activities and measurements are practical for wider use.
-
Cannabidiol suppositories for sexual pain
This project will test whether cannabidiol suppositories can reduce sexual pain and improve sexual function and well-being for adults who experience pain during intercourse or masturbation.
-
Family-focused program for caregivers and young adolescents — Phase 3 of FLOURISH
This trial will test whether an optimized Parenting for Lifelong Health program helps adolescents aged 10–14 and their caregivers in Moldova and North Macedonia improve mental health, family relationships, and well-being compared with a waitlist group.
-
Neurofeedback for Well-Being in people waiting for OCD therapy
This study tests whether a neurofeedback program can improve overall well-being for adults on a waitlist for OCD treatment and whether any improvement relates to changes in OCD, PTSD, and trauma-related symptoms.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.