Mental health Other
Conditions
Interventions
Study Design and justification for control arm
The study design is a randomised controlled superiority trial. Researchers will not know treatment allocation to reduce any bias in outcome data. All pa
this estimate allows for a 25% loss of data to follow-up. For the interview part of the study which will be carried out at 20 weeks post-randomisation of participants to the intervention, it is estima
Sponsors
University of Nottingham
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. In part-time/full-time or honorary/voluntary employment seeking access to well-being support through one of the four sites 2. Currently in work (i.e., not on sickness absence) 3. Aged 18 years or over 4. Competent command of verbal and written English language 5. Access to stable internet connection on a pc/laptop/tablet.
Exclusion criteria
Exclusion criteria: 1. Concurrently attending or planning to attend a psychological or well-being programme in the next three months. formal psychotherapy uptake; 2. Current diagnosis of a mental health condition from a GP or mental health professional serious current or previous mental health difficulties 3. Experience of recent significant life events currently causing significant distress These criteria will be picked up by the therapist team who will manually inspect all content on the screening forms and provide alternative/appropriate support if these exclusion criteria are met. The timelines for the occurrence of such events are intentionally left undefined to avoid identifying adverse or other significant events that may not have occurred over the defined period but will still have consequences for the individual.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Self-rated stress measured using the Perceived Stress Scale-14 (PSS-14) score at 6, 12 and 20 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Self-rated depression measured using the Patient Health Questionnaire-9 (PHQ-9) at 6, 12 and 20 weeks 2. Self-rated trauma measured using the International Trauma Questionnaire (ITQ) at 6,12 and 20 weeks 3. Self-rated mindfulness levels measured using the Five Facet Mindfulness Questionnaire (FFMQ) at 6,12 and 20 weeks 4. Self-rated-personal and occupational burnout measured using the Copenhagen Burnout Inventory (CBI) at 6,12 and 20 weeks 5. Self-rated measure of work engagement measured using the Utrecht Work Engagement Scale-9 (UWES-9), at 6,12 and 20 weeks 6. Health-related quality of life measured using the EuroQol EQ-5D-5L at 6, 12 and 20 weeks 7. Measurement of costs from personal, health and social care perspectives measured using an adapted version of the Client Service Receipt inventory at 6, 12 and 20 weeks | — |
Countries
England, United Kingdom
Outcome results
None listed