eLearning for Suicide Prevention

November 25, 2023 updated by: Doyanne Darnell, University of Washington

Formative Evaluation of an eLearning Approach to Suicide Prevention Training

Project WISE (Workplace Integrated Support & Education) includes developmental and pilot research to create an e-learning training in suicide safety planning enhanced with novel skill-building technologies that can be integrated into the routine workflow of nurses serving patients hospitalized for medical, surgical, or traumatic injury reasons. This study pilots an initial version of this eLearning training and collects data on the acceptability of the training and its components as well as engagement of nurses in the training. The evaluation will inform iterations of the training.

Study Overview

Status

Completed

Conditions

Study Type

Interventional

Enrollment (Actual)

19

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Washington
      • Seattle, Washington, United States, 98104
        • Harborview Medical Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Nurses working in acute or intensive care units at Harborview Medical Center

Exclusion Criteria:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Doyanne A Darnell, PhD, University of Washington

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2021

Primary Completion (Actual)

March 1, 2023

Study Completion (Actual)

March 1, 2023

Study Registration Dates

First Submitted

October 8, 2021

First Submitted That Met QC Criteria

December 15, 2021

First Posted (Actual)

January 5, 2022

Study Record Updates

Last Update Posted (Estimated)

December 18, 2023

Last Update Submitted That Met QC Criteria

November 25, 2023

Last Verified

November 1, 2023

More Information

Terms related to this study

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)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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