Adapting and piloting the ‘Belonging’ student and teacher brief intervention to build school belonging, promote mental health and prevent violence in English secondary schools
| ISRCTN | ISRCTN42905165 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN42905165 |
| ClinicalTrials.gov (NCT) | Nil known |
| Clinical Trials Information System (CTIS) | Nil known |
| Protocol serial number | NIHR160965 |
| Sponsor | London School of Hygiene & Tropical Medicine |
| Funder | National Institute for Health and Care Research |
- Submission date
- 03/02/2025
- Registration date
- 18/02/2025
- Last edited
- 03/11/2025
- Recruitment status
- Recruiting
- Overall study status
- Ongoing
- Condition category
- Other
Plain English summary of protocol
Background and study aims
Poor mental health, violence, school exclusion, and substance use are common issues among young people. Schools can help prevent these problems by improving students' sense of belonging. However, current efforts in English secondary schools can be time-consuming for teachers. Studies in the US show that simpler, shorter interventions can help students feel they belong, benefiting their education and health. This study aims to adapt these US interventions for English secondary schools.
Who can participate?
Students in year 9 (ages 13-14 years) and their teachers from six English secondary schools will participate in the study.
What does the study involve?
The study will start with surveys of students and teachers in May/June 2025, asking about mental health, bullying, and substance use. Four schools will be randomly chosen to receive the new intervention, while two will continue as usual for comparison. In the intervention schools, students will have two classroom sessions to learn that school challenges are normal and don't mean they don't belong. Teachers will have two online training sessions to learn empathetic approaches to student misbehavior. Observations, surveys, and interviews will be conducted throughout the school year to see how the intervention is going. After one year, the surveys will be repeated.
What are the possible benefits and risks of participating?
Students who participate in the intervention group may benefit in terms of improved mental health. Teachers who participate in the intervention group may benefit in terms of reduced burn-out. There are minimal risks of trial participants being upset by some of the questions they answer on mental health and bullying.
Where is the study run from?
The study is run by the London School of Hygiene & Tropical Medicine.
When is the study starting and how long is it expected to run for?
January 2025 to September 2026
Who is funding the study?
The study is funded by the National Institute for Health and Care Research (UK)
Who is the main contact?
Professor Chris Bonell, chris.bonell@lshtm.ac.uk
Contact information
Public, Scientific, Principal investigator
15-17 Tavistock Place
London
WC1H 9SH
United Kingdom
| 0000-0002-6253-6498 | |
| Phone | +44 2076368636 |
| chris.bonell@lshtm.ac.uk |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Interventional randomized controlled trial |
| Secondary study design | Cluster randomised trial |
| Study type | Participant information sheet |
| Scientific title | Optimisation and pilot RCT of the ‘Belonging’ brief intervention to build school belonging, promote mental health and prevent violence in secondary schools |
| Study objectives | 1. Is it possible to combine the US Student Belonging intervention and the Teacher Empathetic Discipline interventions, culturally optimized for English secondary schools and branded as the Belonging intervention? 2. Is progression to a phase III RCT justified in terms of pre-specified criteria concerning intervention and trial feasibility and acceptability? 3. Are outcome and covariate measures well completed and reliable? 4. With what rates are schools recruited and retained? 5. What do qualitative data suggest about how context influences implementation and interacts with intervention mechanisms? 6. Are any potential harms suggested and how might these be mitigated? 7. What is usual practice in control schools? 8. Are methods for economic evaluation feasible? |
| Ethics approval(s) |
Submitted 24/01/2025, London School of Hygiene & Tropical Medicine Intervention Research Ethics Committee (Keppel Street, London, WC1E 7HT, United Kingdom; +44 (0)20 7636 8636; ethics@lshtm.ac.uk), ref: 31596 |
| Health condition(s) or problem(s) studied | Promotion of mental health and prevention of violence and substance use |
| Intervention | Intervention All year-9 students receive two x 15-20-minute classroom sessions early in year 9 working through the student booklet. Students are offered the idea that educational challenges and worries are normal, and not indicative of a lack of belonging. Teachers complete two x online sessions (45, 25 minutes). In the first, teachers read an introduction and student stories describing their experiences in school and relationships with teachers, then respond to writing prompts. In the second, they read a teacher’s story and respond to writing prompts. Comparator This will be treatment as usual with schools continuing with existing activities to promote student mental health and prevent violence and bullying. Process evaluation will describe this. PPIE suggests that no UK schools currently use interventions resembling those proposed. Random allocation After baseline surveys, schools will be randomly allocated 2:1 to intervention and control by the London School of Hygiene & Tropical Medicine clinical trials unit (CTU), stratified by free school meals. A 2:1 allocation in the pilot RCT will enable us to pilot randomisation while ensuring sufficient diversity of schools in the intervention arm for intervention piloting. Schools will be given unique study numbers to preserve allocation concealment within the CTU. The CTU will pass on allocations to the fieldwork team who will then inform schools. Follow-up We will conduct follow-up surveys at 12 months post-baseline (Jun-Jul 2026) with students at the end of year 9 (paper questionnaire) plus all teachers (online questionnaire). NB. Baseline surveys will be done pre-randomisation with year-8 students aged 12-13 and teachers in June/July 2025. |
| Intervention type | Behavioural |
| Primary outcome measure(s) |
Current primary outcome measures as of 03/11/2025: |
| Key secondary outcome measure(s) |
The study will assess primary and secondary outcome measures for use in a phase III trial: |
| Completion date | 30/09/2026 |
Eligibility
| Participant type(s) | Healthy volunteer, Learner/student |
|---|---|
| Age group | Child |
| Lower age limit | 12 Years |
| Upper age limit | 13 Years |
| Sex | All |
| Target sample size at registration | 1200 |
| Key inclusion criteria | The study population is defined as students in year 8 (aged 12-13 years) at baseline plus all teachers. All student-reported measures are suitable for students in this age-group. The research will be inclusive, including of special educational needs and disability (SEND) students. No students deemed competent by teachers to complete data collection will be excluded from recruitment unless they do not consent to, or their parents withdraw them from, the research. Those who have mild learning disabilities or limited English will be supported to complete the questionnaire by researchers. |
| Key exclusion criteria | Students not deemed competent by teachers to complete data collection. |
| Date of first enrolment | 01/03/2025 |
| Date of final enrolment | 30/06/2026 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
London
WC1H 9SH
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | Yes |
|---|---|
| IPD sharing plan summary | Available on request |
| IPD sharing plan | The datasets generated and/or analysed during the current study will be available on reasonable request to the PI supported by a protocol and ethics committee approval. chris.bonell@lshtm.ac.uk |
Study outputs
| Output type | Details | Date created | Date added | Peer reviewed? | Patient-facing? |
|---|---|---|---|---|---|
| Participant information sheet | Participant information sheet | 11/11/2025 | 11/11/2025 | No | Yes |
| Protocol file | 17/01/2025 | 04/02/2025 | No | No | |
| Protocol file | version 1.1 | 03/11/2025 | No | No |
Additional files
- 46786 Belonging pilot trial study protocol version 1.0 17Jan25.pdf
- Protocol file
- ISRCTN42905165_PROTOCOL_V1.1.pdf
- Protocol file
Editorial Notes
03/11/2025: Protocol uploaded, primary outcome measures updated.
04/02/2025: Trial's existence confirmed by the National Institute for Health and Care Research (NIHR) (UK).