Improvement of mental health literacy Mental and Behavioural Disorders
Conditions
Interventions
Forty children and young people aged 12-14 years will be recruited across four study sites (community and educational settings). Ten young people will be recruited per site (cluster).
The interventi
Sponsors
University of Manchester
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Aged between 12 and 14 years old 2. Attending the study site 3. Access to a smartphone/tablet to use the application
Exclusion criteria
Exclusion criteria: 1. Aged under 12 years old and over 14 years old 2. Not attending the study sites 3. No access to smartphone/tablet
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Feasibility measured using children and young people recruitment and retention rates, intervention uptake and engagement rates, and the variability and potential floor/ceiling effects in our proposed patient outcome measures at baseline (prior to randomisation), post-intervention (or at approximately 6 weeks post-randomisation for control group participants) and 3-month follow-up. 2. Mental health literacy is measured using the Knowledge and Attitudes to Mental Health Scale (KAMHS) at baseline, post-intervention and 3-month follow-up | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Core depressive symptoms measured using the short version of the Mood and Feeling Questionnaire (MFQ) at baseline, post-intervention and 3-month follow-up 2. Well-being measured using the World Health Organisation Five Well-Being Index (WHO-5) at baseline, post-intervention and 3-month follow-up 3. Levels of anxiety measured using the Revised Children's Anxiety and Depression Scale (RCADS) at baseline, post-intervention and 3-month follow-up 4. Family cohesion and adaptability measured using the Family Cohesion and Satisfaction with Communication sub-scales of the Family Adaptability and Cohesion Evaluation Scale (FACESIV) at baseline, post-intervention and 3-month follow-up 5. Health status measured using the SF-36 questionnaire at baseline, post-intervention and 3-month follow-up | — |
Countries
England, United Kingdom
Outcome results
None listed