Suicide Prevention Training for PC Providers-in-training
Completed · Not applicable
Conditions studied: Suicide Prevention
In brief
This randomized control study responds to the need for effective suicide prevention education/training that is grounded in adult learning theory and advances in education, in the context of a changing health care landscape where primary care providers are likely to encounter suicidal individuals. The study will test the effectiveness of suicide prevention education for providers-in-training by comparing two conditions: 1) A Control learning group: includes suicide prevention didactics (Commitment to Living: Primary Care) delivered online via brief videos, and 2) An Experimental learning group: includes didactics plus two standardized patient (SP) interactions. One Experimental learning group SP interaction will be in person and the other will be conducted remotely using a secure webcam service (OoVoo). All SP interactions will be recorded. Both groups will be compared in terms of their suicide prevention skills using an SP 'test case' at 6-month follow up. The primary research question is to learn about the impact of practice (though SP simulation) over and above didactics alone.
Key facts
- Study ID
- NCT02996344
- Run by
- University of Rochester
- People needed
- 132
- Starts
- 2016-03-15
- Expected to finish
- 2018-06-07
- Last updated by the study team
- 2020-02-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- trainee in family medicine residency, pediatrics residency, or nurse practitioner program at URMC.
- speaks/writes English.
You may not qualify if…
- on academic probation
Where it is running
- University of Rochester Medical Center — Rochester, New York, United States
Full record on ClinicalTrials.gov
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