Virtual Training Role-Plays to Improve Patient Suicide Outcomes in Primary Care Settings
- Conditions
- Suicidal Ideation
- Interventions
- Other: Web-based training Product
- Registration Number
- NCT03207217
- Lead Sponsor
- SIMmersion, LLC
- 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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 91
(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.
(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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Phase II Efficacy Web-based training Product - Phase I Knowledge Assessment Web-based training Product - Phase II Acceptability Web-based training Product -
- Primary Outcome Measures
Name Time Method 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;
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
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
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
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
- Secondary Outcome Measures
Name Time Method