Trial Outcomes & Findings for Zero Suicide Implementation in Outpatient Mental Health Clinics (NCT NCT05587530)
NCT ID: NCT05587530
Last Updated: 2025-12-30
Results Overview
Acceptability of the treatment engagement and retention intervention for suicidal clients, as rated by clients receiving the intervention and peer specialists delivering the intervention on an assessment adapted from the Treatment Acceptability and Preference Questionnaire
TERMINATED
NA
7 participants
1 month
2025-12-30
Participant Flow
No participants progressed beyond Phase 1 (qualitative interviews)
Participant milestones
| Measure |
Treatment Engagement and Retention Intervention for Suicidal Clients
Participants will receive the manualized treatment engagement and retention protocol for suicidal outpatient clients (single-arm intervention pilot). The manualized treatment engagement and retention protocol will be based on client and staff stakeholder preferences, informed by data from qualitative participatory interviews and secondary data analysis of administrative databases (conducted in phase 1).
Treatment engagement and retention intervention for suicidal clients: The manualized behavioral intervention for treatment engagement and retention of suicidal clients will be based on client and staff stakeholder preferences, informed by data from qualitative participatory interviews and secondary data analysis of administrative databases (conducted in phase 1). In addition to factors identified by stakeholders, if deemed feasible and acceptable during phase 1, the intervention will include structured phone outreach, shared decision-making, and peer support.
|
|---|---|
|
Overall Study
STARTED
|
7
|
|
Overall Study
Staff
|
5
|
|
Overall Study
Clients
|
2
|
|
Overall Study
COMPLETED
|
7
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Zero Suicide Implementation in Outpatient Mental Health Clinics
Baseline characteristics by cohort
| Measure |
Phase 1 Staff Participants
n=5 Participants
Staff members who completed Phase 1 qualitative interviews
|
Phase 1 Client Participants
n=2 Participants
Clients who completed Phase 1 qualitative interviews.
|
Total
n=7 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=174 Participants
|
0 Participants
n=166 Participants
|
0 Participants
n=167 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
5 Participants
n=174 Participants
|
2 Participants
n=166 Participants
|
7 Participants
n=167 Participants
|
|
Age, Categorical
>=65 years
|
0 Participants
n=174 Participants
|
0 Participants
n=166 Participants
|
0 Participants
n=167 Participants
|
|
Sex: Female, Male
Female
|
5 Participants
n=174 Participants
|
2 Participants
n=166 Participants
|
7 Participants
n=167 Participants
|
|
Sex: Female, Male
Male
|
0 Participants
n=174 Participants
|
0 Participants
n=166 Participants
|
0 Participants
n=167 Participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
0 Participants
n=174 Participants
|
0 Participants
n=166 Participants
|
0 Participants
n=167 Participants
|
|
Race (NIH/OMB)
Asian
|
0 Participants
n=174 Participants
|
0 Participants
n=166 Participants
|
0 Participants
n=167 Participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=174 Participants
|
0 Participants
n=166 Participants
|
0 Participants
n=167 Participants
|
|
Race (NIH/OMB)
Black or African American
|
0 Participants
n=174 Participants
|
0 Participants
n=166 Participants
|
0 Participants
n=167 Participants
|
|
Race (NIH/OMB)
White
|
5 Participants
n=174 Participants
|
1 Participants
n=166 Participants
|
6 Participants
n=167 Participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=174 Participants
|
0 Participants
n=166 Participants
|
0 Participants
n=167 Participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=174 Participants
|
1 Participants
n=166 Participants
|
1 Participants
n=167 Participants
|
|
Ethnicity (NIH/OMB)
Hispanic or Latino
|
0 Participants
n=174 Participants
|
1 Participants
n=166 Participants
|
1 Participants
n=167 Participants
|
|
Ethnicity (NIH/OMB)
Not Hispanic or Latino
|
5 Participants
n=174 Participants
|
1 Participants
n=166 Participants
|
6 Participants
n=167 Participants
|
|
Ethnicity (NIH/OMB)
Unknown or Not Reported
|
0 Participants
n=174 Participants
|
0 Participants
n=166 Participants
|
0 Participants
n=167 Participants
|
PRIMARY outcome
Timeframe: 1 monthPopulation: The study was terminated before participants could receive the intervention, therefore no data was collected for this outcome.
Acceptability of the treatment engagement and retention intervention for suicidal clients, as rated by clients receiving the intervention and peer specialists delivering the intervention on an assessment adapted from the Treatment Acceptability and Preference Questionnaire
Outcome measures
Outcome data not reported
PRIMARY outcome
Timeframe: 1 monthPopulation: The study was terminated before participants could receive the intervention, therefore no data was collected for this outcome.
Feasibility of the treatment engagement and retention intervention for suicidal clients, as rated by clients receiving the intervention and peer specialists delivering the intervention on an assessment adapted from the Treatment Acceptability and Preference Questionnaire
Outcome measures
Outcome data not reported
PRIMARY outcome
Timeframe: 1 monthPopulation: The study was terminated before participants could receive the intervention, therefore no data was collected for this outcome.
Satisfaction with the treatment engagement and retention intervention for suicidal clients, as rated by clients receiving the intervention and peer specialists delivering the intervention on an assessment adapted from Treatment Acceptability and Preference Questionnaire
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 1 monthPopulation: The study was terminated before participants could receive the intervention, therefore no data was collected for this outcome.
Perceived effectiveness of the treatment engagement and retention intervention for suicidal clients, as rated by clients receiving the intervention and peer specialists delivering the intervention
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 1 monthPopulation: The study was terminated before participants could receive the intervention, therefore no data was collected for this outcome.
Rate of return after the first OBH visit for clients assigned to the suicide care pathway, as assessed by Medicaid claims
Outcome measures
Outcome data not reported
Adverse Events
Treatment Engagement and Retention Intervention for Suicidal Clients
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place