Feasibility and Acceptability of the Social Prescribing Program, Youth Mental Health and Wellbeing
Conditions
Keywords
social prescribing, children and youth mental health, intervention, wellbeing
Brief summary
The goal of this clinical trial is to learn if the Social Prescription (SP) intervention helps improve mental health and wellbeing in youth. It will also assess the feasibility and acceptability of implementing SP in a community setting. The main questions it aims to answer are: * Is the SP intervention feasible and acceptable for youth, caregivers, and staff? * Does the SP intervention improve mental health outcomes, reduce stress, and increase wellbeing and social connectedness in youth? Researchers will compare the Social Prescription (SP) intervention to an education control group to evaluate its effectiveness in improving youth mental health and wellbeing. Participants will: * Be randomized to receive either the SP intervention or be placed in an education control group * Complete wellbeing and mental health questionnaires at the beginning of the study and again after 12 weeks * Participate in qualitative interviews to share their experiences after participating in SP
Interventions
BEHAVIORALSocial Prescribing
A social prescribing intervention is a non-clinical approach to improving health and wellbeing by connecting individuals to community-based services and activities that address social, emotional, and practical needs. These may include arts programs, physical activity, peer support, volunteering, or nature-based activities. Facilitated by a link worker or navigator, social prescribing is tailored to the individual and aims to enhance mental health, reduce isolation, and support overall wellness beyond traditional medical care.
Sponsors
Children's Hospital of Eastern Ontario Research Institute
University of Ottawa
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
11 Years to 17 Years
Healthy volunteers
No
Inclusion criteria
* between 11-17 years of age * on the waitlist for mental health services * are not an immediate safety threat to themselves or others as assessed by the HEADS ED questionnaire
Exclusion criteria
* Children \< 11 years old * Adolescents \> 17 years old
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Student Resilience Survey | From enrollment to end of treatment or control period at 12 weeks | Student Resilience Survey measuring students' perceptions of their individual characteristics as well as protective factors embedded in the environment: |
| Perceived Stress Scale | From enrollment to end of treatment or control period at 12 weeks. | The Perceived Stress Scale is a widely used to help understand how different situations affect our feelings and our perceived stress. |
| Warwick-Edinburgh Mental Wellbeing Scale | From enrollment to end of treatment or control period at 12 weeks | The Warwick-Edinburgh Mental Wellbeing Scale (WEMWBS) was developed to enable the monitoring of mental wellbeing in the general population and the evaluation of projects, programmes and policies which aim to improve mental wellbeing. |
| Social Connectedness Scale | From enrollment to end of treatment or control period at 12 weeks | The Social Connectedness Scale measures the extent to which individuals feel connected to others in their social environment. |
| Revised Children's Anxiety and Depression Scale | From enrollment to end of treatment or control period at 12 weeks. | The Revised Children's Anxiety and Depression Scale (RCADS) is a self-report questionnaire that measures symptoms of anxiety and depression in children and adolescents aged 8 to 18. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Intervention Appropriateness Measure | From enrollment to end of treatment or control period at 12 weeks | The Intervention Appropriateness Measure assesses the perceived relevance or suitability of an intervention for a specific setting or population. |
| Feasibility of Intervention Measure | From enrollment to end of treatment or control period at 12 weeks | The Feasibility of Intervention Measure gauges how practical and possible it is to implement an intervention within a given setting. |
| Acceptability of Intervention Measure | From enrollment to end of treatment or control period at 12 weeks | The Acceptability of Intervention Measure evaluates how agreeable or satisfactory an intervention is perceived to be by participants or implementers. |
Countries
Canada
Contacts
Primary ContactSusan Bennett, PhD
Backup ContactOlivia MacLeod, PhD
Outcome results
None listed