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

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.
Overall Study
STARTED
28
Overall Study
COMPLETED
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

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.
Age, Continuous
55.9 years
STANDARD_DEVIATION 14.9 • n=5 Participants
Sex/Gender, Customized
Gender · Cisgender male
24 Participants
n=5 Participants
Sex/Gender, Customized
Gender · Cisgender female
4 Participants
n=5 Participants
Race/Ethnicity, Customized
Race / Ethnicity · African American / Black
1 Participants
n=5 Participants
Race/Ethnicity, Customized
Race / Ethnicity · White
24 Participants
n=5 Participants
Race/Ethnicity, Customized
Race / Ethnicity · Other
2 Participants
n=5 Participants
Race/Ethnicity, Customized
Race / Ethnicity · missing
1 Participants
n=5 Participants
Region of Enrollment
United States
28 Participants
n=5 Participants

PRIMARY outcome

Timeframe: baseline

Perspectives on VA-based interventions that aim to reduce access to firearms and medications.

Outcome measures

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.
Qualitative Theme Among 28 Patients on Perspectives on Lethal Means Interventions
Acceptability
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
Qualitative Theme Among 28 Patients on Perspectives on Lethal Means Interventions
Influence of prior opioid exposure
12 participants

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

Joseph Simonetti

Veterans Health Administration

Phone: 7207236491

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place