Assisting in Decisions in Emergency Departments: (ED-AID) Study

Sponsor
University of Colorado, Denver (Other)
Overall Status
Completed
CT.gov ID
NCT03478501
Collaborator
Harvard School of Public Health (HSPH) (Other), Denver Health and Hospital Authority (Other), National Institute of Mental Health (NIMH) (NIH)
49
3
2
9.6
16.3
1.7

Study Details

Study Description

Brief Summary

This study will test a patient decision aid about safe firearm storage during suicidal crisis. The investigators hypothesize that participants with higher quality decisions after the decision aid will be more likely to change their firearm storage to reduce access during the time of crisis.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Decision Aid
N/A

Detailed Description

Limiting access to a firearms during suicidal crisis can save lives. This study will test a patient decision aid about safe firearm storage during crisis. The investigators will enroll 60 adult emergency department patients being evaluated for suicidal risk and have at least one firearm at home. If available, the investigators will also enroll a family member or friend. Participants will randomly receive one of two things: the decision aid or general suicide prevention information. A week later, the investigators will call participants to see how both groups choose to store their firearms. This trial tests the acceptability of the decision aid, effects on decision making, effect on home storage, effect on suicide outcomes, and feasibility of a larger trial. The investigators hypothesize that participants with higher quality decisions after the decision aid will be more likely to change their firearm storage to reduce access during the time of crisis; should the pilot demonstrate feasibility, in a subsequent larger trial this hypothesis would be tested directly.

Study Design

Study Type:
Interventional
Actual Enrollment :
49 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Assisting in Informing Decisions in Emergency Departments: (ED-AID) Study
Actual Study Start Date :
Jun 20, 2018
Actual Primary Completion Date :
Apr 9, 2019
Actual Study Completion Date :
Apr 9, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Decision Aid Group

Participants randomized to this arm will view the decision aid on a tablet in the emergency department.

Behavioral: Decision Aid
This intervention is a tablet based Lethal Means Decision Aid with proposed use to augment lethal means counseling in emergency departments for patients at risk of suicide.

No Intervention: Control Group

Participants randomized to this arm will be asked to review general suicide prevention information on a tablet in the emergency department.

Outcome Measures

Primary Outcome Measures

  1. Acceptability of Lethal Means Decision Aid [Baseline]

    This will be assessed using the Ottawa Acceptability Questionnaire that captures the patient's feedback on the design, presentation, quality, and information presented in the decision aid through both survey and open ended questions. Questions include likert scale responses (range of responses are specific to each question's content). There are also a series of yes/no/don't know questions related to content presented. Each "no" response asks the participant to elaborate in an open ended response. The participant also has the ability to provide general feedback in open ended feedback format. There are no subscales to this measure.

  2. Decision Making Quality in Emergency Department (ED) [Baseline]

    The Decisional Conflict Scale (DCS), low literacy 10 item scale, measures decision quality, uncertainty, personal perceptions and satisfaction. A total score is computed through sum of items 1-10 (Yes=1; unsure=2; no=4) divided by 10, and multiplied by 25. Scores range from 0 (no decision conflict) to 100 (extreme decision conflict). The sum of items 1, 2, 3, divided by 3 and multiplied by 25 is the informed decision subscale (1 extremely informed) to 100 extremely uninformed). The sum of items 4 and 5, divided by 2 and multiplied by 25 is the values clarity (0 feels extremely clear to 100 feels extremely unclear). The sum of items 9 and 10, divided by 2 and multiplied by 25 is the uncertainty subscale (0 feels extremely certain about best choice to 100 feels extremely uncertain about best choice). The sum of items 6, 7, 8, divided by 3 and multiplied by 25 is the support subscale (0 feels extremely supported in decision making to 100 feels extremely unsupported in decision making).

  3. Home Firearm Storage [Baseline and 1 week follow up]

    At both baseline and one week follow up, participants will complete a study specific survey that asks about how they currently store their firearms or current plans to change how they store their firearms to measure change in storage.

  4. Decision Making Quality - Follow up [1 week follow up]

    The Decisional Conflict Scale (DCS), low literacy 10 item scale, measures decision quality, uncertainty, personal perceptions and satisfaction. A total score is computed through sum of items 1-10 (Yes=1; unsure=2; no=4) divided by 10, and multiplied by 25. Scores range from 0 (no decision conflict) to 100 (extreme decision conflict). The sum of items 1, 2, 3, divided by 3 and multiplied by 25 is the informed decision subscale (1 extremely informed) to 100 extremely uninformed). The sum of items 4 and 5, divided by 2 and multiplied by 25 is the values clarity (0 feels extremely clear to 100 feels extremely unclear). The sum of items 9 and 10, divided by 2 and multiplied by 25 is the uncertainty subscale (0 feels extremely certain about best choice to 100 feels extremely uncertain about best choice). The sum of items 6, 7, 8, divided by 3 and multiplied by 25 is the support subscale (0 feels extremely supported in decision making to 100 feels extremely unsupported in decision making).

  5. Suicidal Ideation and Behavior at One Month [1 month post baseline]

    While this pilot trial is not powered to detect a change in mental health outcomes, as part of the feasibility for a larger trial, the investigators will attempt to track suicide attempts and outcomes through medical record chart review.

  6. Suicidal Ideation and Behavior at Three Months [3 months post baseline]

    While this pilot trial is not powered to detect a change in mental health outcomes, as part of the feasibility for a larger trial, the investigators will attempt to track suicide attempts and outcomes through medical record chart review.

  7. Vital Statistics (Suicide death) [3 months post baseline]

    While this pilot trial is not powered to detect a change in suicide outcomes, as part of the feasibility for a larger trial, the investigators will attempt to track suicide death outcomes through state vital statistics reporting.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 89 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Being evaluated in the emergency department for suicidal ideation/suicide attempt

  • Deemed medically stable by ED physician

  • Age greater than or equal to 18 years old

  • Able and willing to have telephone follow up at 1 week

  • Report at least one firearm in the home

Exclusion Criteria:
  • Unable to participate medically or cognitively (e.g. sustained altered level of consciousness, hostility, psychosis, sexual assault victim, severe vomiting or pain)

  • Currently in legal custody

  • Live in group home or other supervised custody

  • Already enrolled

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Colorado Hospital Aurora Colorado United States 80045
2 Memorial Hospital Colorado Springs Colorado United States 80909
3 Denver Health Denver Colorado United States 80204

Sponsors and Collaborators

  • University of Colorado, Denver
  • Harvard School of Public Health (HSPH)
  • Denver Health and Hospital Authority
  • National Institute of Mental Health (NIMH)

Investigators

  • Principal Investigator: Marian Betz, MD, MPH, University of Colorado, Denver

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
University of Colorado, Denver
ClinicalTrials.gov Identifier:
NCT03478501
Other Study ID Numbers:
  • 17-2299
  • R34MH113539-01
First Posted:
Mar 27, 2018
Last Update Posted:
Jun 24, 2021
Last Verified:
Jun 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Colorado, Denver
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 24, 2021