during admission | at discharge | 1 w after discharge | 4 w | 8 w | 12 w | 6 m | 12 m | 18 m | 24 m | 30 m | 36 m | 42 m | Interim/Final analysis | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Psychiatric diagnosis | â—Ž | |||||||||||||
Psychoeducation 1* | â—Ž | |||||||||||||
Informed consent | â—Ž | |||||||||||||
Enrollment/randomization | â—Ž | |||||||||||||
Input data at time of discharge | â—Ž | |||||||||||||
Case management (Psychodeucation 2**, others) | â—‹ | â—‹ | â—‹ | â—‹ | â—‹ | â—‹ | â—‹ | â—‹ | â—‹ | â—‹ | â—‹ | â—‹ | ||
Psychiatric evaluation | â—Ž | â—Ž | â—Ž | â—Ž | â—Ž | |||||||||
Event | Input content of the event (ie, recurrent suicidal behavior, adverse event) into the web system as occasions require | |||||||||||||
Participant survival (or cause of death of the participant) | â—Ž | |||||||||||||
Actions to critical situations | In both groups during the study as occasions require | |||||||||||||
Reports of a serious adverse event | Prompt report to the director of the hospital and the study group management office in both groups as occasions require |