Suicidal Ideation Clinical Trial
Official title:
Written Safety Planning vs the Safety Net App: A Prospective Randomized Pilot Trial
Verified date | February 2023 |
Source | University of Arkansas |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Safety planning is a brief, ED-feasible intervention which has been demonstrated to save lives and has been universally recommended by every recent expert consensus panel on suicide prevention strategies. In one popular version of the safety plan developed by Stanley et al, the patient is encouraged to write out the following items: identifying personal signs of a crisis; helpful internal coping strategies; social contacts or settings which may distract from a crisis; using family members or friends for help when in crisis; mental health professionals who can be contacted when in crisis; and restricting access to lethal means. This study aims to find out how valuable an electronic safety plan is compared to a traditional paper safety plan. People who are visiting the emergency department for thoughts of self-harm will be asked to participate.
Status | Completed |
Enrollment | 30 |
Est. completion date | December 28, 2020 |
Est. primary completion date | December 28, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 89 Years |
Eligibility | Inclusion Criteria: - Patients presenting for suicidal ideation (SI) or after a suicide attempt to the UAMS ED - Willingness to engage in safety planning with trained non-clinical staff - Have not already filled out a safety plan at the current visit Exclusion Criteria: - <18 or >89 years of age - Incarcerated or in police custody - Non-English-speaking or Non-English-writing (as translators will not be available for this study) - Critically-ill (or appear to be critically-ill) - Intoxicated with alcohol or other substance(s) - ED staff objection to patient enrollment in study - Unwilling or unable to complete the safety plan electronically - Unwilling or unable to use a tablet device to complete the safety plan - Unwilling or unable to show/email the safety plan to clinical and research staff |
Country | Name | City | State |
---|---|---|---|
United States | University of Arkansas for Medical Sciences | Little Rock | Arkansas |
Lead Sponsor | Collaborator |
---|---|
University of Arkansas |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Acceptability of Intervention | The number of patients approached who agree to allow trained non-clinical staff to assist with safety planning. | Up to 12 hours | |
Primary | Length of Stay | The length of stay in the ED for patients approached who agree to allow trained non-clinical staff to assist with safety planning. | Up to 12 hours | |
Primary | Satisfaction With Safety Planning | Evaluate patient satisfaction with safety planning. This will be assessed by having the patient rate their experience with the safety planning process on a 7-point Likert scale (1 - strongly disagree; 2 - disagree; 3 - moderately disagree; 4 - neutral; 5 - moderately agree; 6 - agree; 7 - strongly agree). A Likert scale measures how much someone disagrees or agrees with a particular statement. | Up to 12 hours |
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