Quantitative (Consumer) data collected in the cRCT | |
---|---|
Primary outcome | 1. Questionnaire about the Process of Recovery (QPR) |
Secondary outcomes | 2. INSPIRE questionnaire [13] 3. Warwick-Edinburgh Mental Well-being Scale (WEMWBS) [36] |
Other measures | 4. Participant Demographic Record 5. Health economic record 6. Days out of role 7. Days absent from work 8. Service utilization questionnaire 9. The Perceived Need for Care Questionnaire (PNCQ) [38] 10. Client Satisfaction Questionnaire [39] 11. Mind Australia Satisfaction Survey [40] 12. The Coercion Ladder [41] 13. Global Assessment of Functioning Scale [42] 14. Social and Occupational Functioning Assessment Scale [42, 43] |
15. Routinely collected information in service medical files (data in the year prior to interview): | |
 | Health of the Nation Outcome Scales (HoNoS; 12 item clinician-rated measure of social disability) [39]; |
 | Basis 32 (consumer-rated); |
 | LSP16 (clinician-rated); and Focus of Care (clinician-rated). |
 | Diagnosis information |
 | Number of community/outpatient mental health contacts: • Care teams involved (discipline) • Location of contact • Date and time of contact • Focus of care for the above |
 | Number of inpatient mental health admissions: • Inpatient facility type, and Length of Stay (LOS) • Legal status e.g. involuntary admission, etc. Any other relevant mental health related data recorded in electronic file. |
Qualitative (Consumers and staff) sub-study data | |
Consumer qualitative data | |
 Individual interviews |  |
 Focus groups |  |
Staff qualitative data | |
 Individual interviews |  |
 Focus groups |  |
Process evaluation sub-study dataa |