- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05178121
eLearning for Suicide Prevention
Formative Evaluation of an eLearning Approach to Suicide Prevention Training
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Washington
-
Seattle, Washington, United States, 98104
- Harborview Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Nurses working in acute or intensive care units at Harborview Medical Center
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Project WISE eLearning Training in Suicide Safety Planning
|
The training includes a web-based didactic in suicide safety planning, interactive practice in counseling microskills with a chat bot, role-playing safety planning with a standardized patient, and reviewing automated feedback on safety planning counseling skills generated from a computer coding system.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Training Acceptability Self-Report - Post-Training
Time Frame: Immediately after completing the training
|
A 4-item self-report measure created for this study will assess satisfaction with all of the training components using a Likert-type scale of 0 = Not at all satisfied to 4 = Completely satisfied.
|
Immediately after completing the training
|
|
Training Acceptability Self-Report - 6-Month Follow-up
Time Frame: 6-months after completing the training
|
A 4-item self-report measure created for this study will assess satisfaction with all of the training components using a Likert-type scale of 0 = Not at all satisfied to 4 = Completely satisfied.
|
6-months after completing the training
|
|
Training Engagement Self-Report - Post-Training
Time Frame: Immediately after participants indicate they have completed the training activities
|
Investigators will collect self-reported completion of the training activities using a 4-item measure.
Participants will report on a sliding scale from 0-100, what percent of each training activity they believe they completed.
|
Immediately after participants indicate they have completed the training activities
|
|
Participant Retention
Time Frame: 6 Months after completing the training
|
Percent of participants retained throughout study follow-up
|
6 Months after completing the training
|
|
Training Acceptability - System Usability Scale for Client Bot Emily
Time Frame: Once, immediately after engaging with each of the training technologies
|
The System Usability Scale, a self-report measure using a Likert-type rating scale, will assess acceptability of the two technologic training components: Client Bot Emily and Lyssn Advisor. Client Bot Emily is a virtual patient/chat bot with the persona of a suicidal patient. Nurses chat with Emily and practice skills of asking open-ended questions and making reflections about statements Emily makes. Lyssn Advisor is an online platform that automatically codes transcripts of audio or video recorded role-plays for counseling skills; nurses then log in to the platform to see their scores, which provides feedback on their counseling performance. Scores on the SUS range from 0-100, which higher scores indicating greater usability or acceptability. |
Once, immediately after engaging with each of the training technologies
|
|
Training Engagement With Client Bot User Data - Post-Training
Time Frame: Immediately after participants indicate they have completing the training activities
|
Data is collected from the technologic platform on whether and how often participants accessed the training technologies.
Engagement is indicated by participants accessing the platform using their unique login and interacting with the webpage associated with the Client Bot.
The unit of measurement will be the number of participants who accessed the Client Bot during the training period.
|
Immediately after participants indicate they have completing the training activities
|
|
Training Engagement With Lyssn Advisor User Data - Post-Training
Time Frame: Immediately after participants indicate they have completing the training activities
|
Data is collected from the technologic platform on whether and how often participants accessed the training technologies.
Engagement is indicated by participants accessing the platform using their unique login and interacting with the webpage associated with the Lyssn Advisor.
The unit of measurement will be the frequency of times participants visits the Lyssn Advisor webpage.
|
Immediately after participants indicate they have completing the training activities
|
|
Training Engagement With Client Bot User Data - 6-Month Follow-up
Time Frame: 6-months after participants indicate they have completed the training activities
|
Data is collected from the technologic platform on whether and how often participants accessed the training technologies.
Engagement is indicated by participants accessing the platform using their unique login and interacting with the webpage associated with the Client Bot.
The unit of measurement will be the number of participants who logged on and interacted with the Client Bot after the training period and before completing the 6-month survey.
|
6-months after participants indicate they have completed the training activities
|
|
Training Engagement With Lyssn Advisor User Data - 6-Month Follow-up
Time Frame: 6-months after participants indicate they have completed the training activities
|
Data is collected from the technologic platform on whether and how often participants accessed the training technologies.
Engagement is indicated by participants accessing the platform using their unique login and interacting with the webpage associated with the Lyssn Advisor.
The unit of measurement will be the frequency of times participants visits the Lyssn Advisor webpage during the 6-month follow-up period.
|
6-months after participants indicate they have completed the training activities
|
|
Client Bot Training Engagement Self-Report - 6 Month Follow-up
Time Frame: 6-months after participants indicate they have completed the training activities
|
Participants will self-report whether or not they accessed any of the training technologies during the follow-up period.
|
6-months after participants indicate they have completed the training activities
|
|
Training Acceptability - System Usability Scale for Lyssn Advisor
Time Frame: Once, immediately after engaging with each of the training technologies
|
The System Usability Scale, a self-report measure using a Likert-type rating scale, will assess acceptability of the two technologic training components: Client Bot Emily and Lyssn Advisor. Client Bot Emily is a virtual patient/chat bot with the persona of a suicidal patient. Nurses chat with Emily and practice skills of asking open-ended questions and making reflections about statements Emily makes. Lyssn Advisor is an online platform that automatically codes transcripts of audio or video recorded role-plays for counseling skills; nurses then log in to the platform to see their scores, which provides feedback on their counseling performance. Scores on the SUS range from 0-100, which higher scores indicating greater usability or acceptability. |
Once, immediately after engaging with each of the training technologies
|
|
Lyssn Advisor Training Engagement Self-Report - 6 Month Follow-up
Time Frame: 6-months after participants indicate they have completed the training activities
|
Participants will self-report whether or not they accessed any of the training technologies during the follow-up period.
|
6-months after participants indicate they have completed the training activities
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Doyanne A Darnell, PhD, University of Washington
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00013577
- K23MH118361-01A1 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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