Trial Outcomes & Findings for Emergency Room Firearm and Medication Safety Intervention (NCT NCT04797221)
NCT ID: NCT04797221
Last Updated: 2024-08-13
Results Overview
Perspectives on VA-based interventions that aim to reduce access to firearms and medications.
Recruitment status
COMPLETED
Target enrollment
28 participants
Primary outcome timeframe
baseline
Results posted on
2024-08-13
Participant Flow
Participant milestones
| Measure |
Study Group
28 Veterans who were recently discharged from a VHA emergency care. Veteran participants were: \>18 years of age, had access to firearms and/or medications at home, and were determined to be at elevated suicide risk based on the presence of suicide risk factors, including screening positive for having elevated suicide risk at the time of admission via the Columbia Suicide Severity Rating Scale Screener. Veterans were excluded if they were critically ill (intensive care unit requirements), are severely cognitively impaired, or had severe psychiatric symptoms that would preclude study participation.
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|---|---|
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Overall Study
STARTED
|
28
|
|
Overall Study
COMPLETED
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28
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Emergency Room Firearm and Medication Safety Intervention
Baseline characteristics by cohort
| Measure |
Study Group
n=28 Participants
28 Veterans who were recently discharged from a VHA emergency care. Veteran participants were: \>18 years of age, had access to firearms and/or medications at home, and were determined to be at elevated suicide risk based on the presence of suicide risk factors, including screening positive for having elevated suicide risk at the time of admission via the Columbia Suicide Severity Rating Scale Screener. Veterans were excluded if they were critically ill (intensive care unit requirements), are severely cognitively impaired, or had severe psychiatric symptoms that would preclude study participation.
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|---|---|
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Age, Continuous
|
55.9 years
STANDARD_DEVIATION 14.9 • n=5 Participants
|
|
Sex/Gender, Customized
Gender · Cisgender male
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24 Participants
n=5 Participants
|
|
Sex/Gender, Customized
Gender · Cisgender female
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4 Participants
n=5 Participants
|
|
Race/Ethnicity, Customized
Race / Ethnicity · African American / Black
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1 Participants
n=5 Participants
|
|
Race/Ethnicity, Customized
Race / Ethnicity · White
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24 Participants
n=5 Participants
|
|
Race/Ethnicity, Customized
Race / Ethnicity · Other
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2 Participants
n=5 Participants
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|
Race/Ethnicity, Customized
Race / Ethnicity · missing
|
1 Participants
n=5 Participants
|
|
Region of Enrollment
United States
|
28 Participants
n=5 Participants
|
PRIMARY outcome
Timeframe: baselinePerspectives on VA-based interventions that aim to reduce access to firearms and medications.
Outcome measures
| Measure |
Study Group
n=28 Participants
28 Veterans who were recently discharged from a VHA emergency care. Veteran participants were: \>18 years of age, had access to firearms and/or medications at home, and were determined to be at elevated suicide risk based on the presence of suicide risk factors, including screening positive for having elevated suicide risk at the time of admission via the Columbia Suicide Severity Rating Scale Screener. Veterans were excluded if they were critically ill (intensive care unit requirements), are severely cognitively impaired, or had severe psychiatric symptoms that would preclude study participation.
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|---|---|
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Qualitative Theme Among 28 Patients on Perspectives on Lethal Means Interventions
Acceptability
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26 participants
|
|
Qualitative Theme Among 28 Patients on Perspectives on Lethal Means Interventions
Uncertainty about intent and efficacy
|
20 participants
|
|
Qualitative Theme Among 28 Patients on Perspectives on Lethal Means Interventions
Cost and convenience are critical
|
24 participants
|
|
Qualitative Theme Among 28 Patients on Perspectives on Lethal Means Interventions
Uncertainty regarding engaging other people in interventions
|
14 participants
|
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Qualitative Theme Among 28 Patients on Perspectives on Lethal Means Interventions
Influence of prior opioid exposure
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12 participants
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Adverse Events
Study Group
Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place