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ED-Home Pilot Study

Primary Purpose

Housing Problems, Drug Use, Alcohol; Use, Problem

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Referral to homelessness prevention services
Substance use services
Follow-up
Sponsored by
NYU Langone Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Housing Problems

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Be a patient in the Bellevue Hospital Center ED.
  • Be ≥18 years old.
  • Screen positive for homelessness risk using a homelessness risk screening tool (HRST).
  • Screen positive for unhealthy alcohol or drug use.
  • Able to provide consent.

Exclusion Criteria:

  • Medically (e.g., critically ill) or psychiatrically unstable.
  • Unable to provide informed consent for other reason (e.g., cognitive deficit, profound intoxication).
  • Incarcerated or in police custody.
  • Unable to understand and speak English.
  • Lives outside NYC and/or cannot give a NYC ZIP code.
  • Already homeless (residing in a shelter or on the streets).
  • Does not have a telephone where can be reached for follow-up.
  • Has already received specialized peer navigator/addiction social worker services during current ED visit.
  • Has already participated in the study.

Sites / Locations

  • New York University School of Medicine

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Homelessness Prevention Services

Arm Description

Outcomes

Primary Outcome Measures

Percentage of Potential Participants Approached Who Were Eligible for the Study
Percentage of Eligible Participants Who Agreed to Participate in the Study
Number of Participants Who Received Referrals for Homelessness Prevention and/or Substance Use Services

Secondary Outcome Measures

Full Information

First Posted
March 4, 2019
Last Updated
July 26, 2022
Sponsor
NYU Langone Health
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT03864341
Brief Title
ED-Home Pilot Study
Official Title
ED-Home: A Pilot Feasibility Study of a Homelessness Prevention Intervention for Substance Using Emergency Department Patients
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
May 8, 2019 (Actual)
Primary Completion Date
March 23, 2020 (Actual)
Study Completion Date
March 23, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NYU Langone Health
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a single-arm pilot study to test the feasibility of homelessness prevention and substance use interventions to be delivered to at-risk patients in the Bellevue Hospital emergency department (ED). ED patients (n=40) found eligible for the study will complete a baseline assessment and receive referrals to appropriate services, with a final six-month follow-up assessment.
Detailed Description
ED patients found eligible for the study will complete a baseline survey and receive one-time, in person services at the time of the baseline/enrollment ED visit including referrals to homelessness prevention and substance use services, with a final six-month follow-up survey. Interim contacts at 7-10 days, 3 months, and 5 months will be used to assure intervention components were received and to confirm participant contact information.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Housing Problems, Drug Use, Alcohol; Use, Problem

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Homelessness Prevention Services
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
Referral to homelessness prevention services
Intervention Description
Referral to Homebase homelessness prevention services offered by community-based organizations in NYC
Intervention Type
Behavioral
Intervention Name(s)
Substance use services
Intervention Description
Referral to substance use services (SBIRT and peer counselor/social work contact) available at Bellevue Hospital
Intervention Type
Behavioral
Intervention Name(s)
Follow-up
Intervention Description
Follow-up to assist participants in receiving homelessness prevention services
Primary Outcome Measure Information:
Title
Percentage of Potential Participants Approached Who Were Eligible for the Study
Time Frame
Month 6
Title
Percentage of Eligible Participants Who Agreed to Participate in the Study
Time Frame
Month 6
Title
Number of Participants Who Received Referrals for Homelessness Prevention and/or Substance Use Services
Time Frame
Month 6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Be a patient in the Bellevue Hospital Center ED. Be ≥18 years old. Screen positive for homelessness risk using a homelessness risk screening tool (HRST). Screen positive for unhealthy alcohol or drug use. Able to provide consent. Exclusion Criteria: Medically (e.g., critically ill) or psychiatrically unstable. Unable to provide informed consent for other reason (e.g., cognitive deficit, profound intoxication). Incarcerated or in police custody. Unable to understand and speak English. Lives outside NYC and/or cannot give a NYC ZIP code. Already homeless (residing in a shelter or on the streets). Does not have a telephone where can be reached for follow-up. Has already received specialized peer navigator/addiction social worker services during current ED visit. Has already participated in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kelly Doran, MD, MHS
Organizational Affiliation
New York Langone Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York University School of Medicine
City
New York
State/Province
New York
ZIP/Postal Code
10016
Country
United States

12. IPD Sharing Statement

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ED-Home Pilot Study

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