Suicidal Ideation
Conditions
Keywords
Safety Planning, Access to Lethal Means, Zero Suicide
Brief summary
SIMmersion, in collaboration with the Institute for Family Health (IFH) and the Educational Development Center (EDC) propose to develop a web-based training product, Suicide Prevention Role-plays for Interactive Training (SPiRIT), a series of 4 modules to train providers to more effectively manage patients who screen positive for risk of suicide in this Phase I/Phase II fast-track application. If funded, the team will develop the Risk Assessment module in Phase I and utilize a within group pre-post design to evaluate its feasibility. Twenty practicing clinicians will be recruited to utilize the module and complete a pre-post knowledge test. In Phase II, the team will develop Safety Planning, Access to Lethal Means, and Willingness to Accept a Referral modules. The efficacy of the product to positively influence patient outcomes will be tested with a Historically Controlled Trial (HCT) enlisting 65 practicing clinicians across five IFH sites. All providers will be trained and patient outcomes will be tracked for 6 months post training. This data set will be compared to 6 months of historical data for the same provider group. Primary outcomes of this study will measure the participants' ability in obtain improved patient outcomes related to: 1) rate of same-day C-SSRS Screening; 2) rate of suicide being added to the problem list; 3) rate of same-day safety planning; 4) rate of same day C-SSRS Lifeline/Recent Completion; 5) rate of same-day Risk Assessment; 6) rate of acceptance and attendance to within-Institute referrals for post intervention patients who are offered the referral at the first visit; 7) and lower rates of documented suicide attempts. Ultimately, the development and successful testing of this product would provide the US health care system a novel technology to scale up a clinician's confidence and skill to better manage patients who identify as at-risk for suicide. Additionally, if effective, this product will have a direct impact on patient outcomes, a vital component to any training product that attempts to train health care professionals. The utility and scalability of the proposed product will move health care systems toward the goal of zero deaths from suicide consistent with the Zero suicide approach.
Interventions
OTHERWeb-based training Product
A series of 4 modules to train providers to more effectively manage patients who screen positive for risk of suicide. The modules are: Risk Assessment, Safety Planning, Access to Lethal Means, and Willingness to accept referral.
Sponsors
The Institute for Family Health
Education Development Center, Inc.
SIMmersion, LLC
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
(1) Hold an active license issued by the State of New York for their profession and be in good standing; (2) actively see patients at an IFH site; and (3) have completed IFH's mandated suicide prevention training.
Exclusion criteria
(1) have not completed their IFH Suicide Prevention Training as outlined in the IFH's Suicide Prevention Training Policy; or (2) have uncorrected vision or hearing problems that prevent the person from using the software. Specific to Phase II an additional criteria is (3)participated in the Phase 1 feasibility testing.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| C-SSRS Screening | Assessment will occur after a 6 month period of tracking patient records for each provider | Higher rates of same-day C-SSRS Screening |
| Suicide addition to Problem List | Assessment will occur after a 6 month period of tracking patient records for each provider | Higher rates of suicide being added to the problem list |
| Same-day Safety Planning, if a positive screen | Assessment will occur after a 6 month period of tracking patient records for each provider | Higher rates of same-day Safety Planning, if a positive screen |
| C-SSRS Lifeline/Recent Completion | Assessment will occur after a 6 month period of tracking patient records for each provider | Higher rates of same-day C-SSRS Lifeline/Recent Completion, if a positive screen; |
| Risk Assessment | Assessment will occur after a 6 month period of tracking patient records for each provider | Higher rates of same-day Risk Assessment, if a positive screen |
| Within-Institute referrals | Assessment will occur after a 6 month period of tracking patient records for each provider | Higher rates of acceptance and attendance to within-Institute referrals for post intervention patients who are offered the referral at the first visit |
| Documented suicide attempts | Assessment will occur after a 6 month period of tracking patient records for each provider | Have lower rates of documented suicide attempts |
Outcome results
None listed