| Exclusion of participants |
Should any potential participants be excluded due to elevated risk of suicide? (Select one) |
No, we should be collecting data from everyone, even those at the highest levels of suicide risk |
90.5% |
| Yes, people who are too high risk should not participate in research |
9.5% |
| Conditions to staying in the study |
Should there be certain conditions participants must agree to in order to enter/stay in a study, such as agreeing that they will go to treatment sessions or call a hotline when at high risk? (Select one) |
No, we can encourage people to do these things but should not set any such conditions |
85.7% |
| Yes, there should be conditions participants must agree to enter/stay in the study |
14.3% |
| Informed Consent |
Should participants be explicitly informed of the following during informed consent? (Select all that apply) |
Whether responses can trigger follow‐up and/or intervention actions by the research team and/or clinicians, which may include breaking of confidentiality |
100% |
| Information that the participant should not rely on the study monitoring to keep them safe/alive |
100% |
| Information about who will have access to their data including third party software developers to improve their app product |
100% |
| How often researchers will check participants' responses |
95.2% |
| Circumstances under which the subject's participation may be terminated by the investigator without regard to the subject's consent |
95.2% |
| Who to contact in case of crisis |
95.2% |
| Information that there can be technology failures |
95.2% |
| Information that the participant won't be automatically hospitalized if their responses trigger a follow up assessment by the research team |
90.5% |
| How and what information will be shared with participants and others if confidentiality is breached |
90.0% |
| What risk monitoring activities and interventions will be taking place |
76.2% |
