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ED Initiated Oral Naltrexone for AUD

Primary Purpose

Alcohol Use Disorder

Status
Recruiting
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Emergency Department Initiated Oral Naltrexone
Sponsored by
Icahn School of Medicine at Mount Sinai
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Alcohol Use Disorder focused on measuring Medication Assisted Treatment, Emergency Department, Naltrexone

Eligibility Criteria

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

Inclusion Criteria:

  • Emergency Department patients 18 years of age or older
  • Treated in the ED during screening hours
  • Moderate to severe AUD as determined by DSM-5 criteria
  • Able to speak and understand English
  • Medically stable for an interview as determined by their primary ED provider
  • Willing and able to consent to study participation
  • Two points of contact available for follow-up

Exclusion Criteria:

  • ED patients younger than 18 years of age
  • Medically or psychiatrically unstable as determined by the ED provider
  • Unable to speak or understand English
  • Unable to provide consent for study participation
  • Past year opioid dependence
  • Urine drug screen positive for opioids
  • Current or anticipated need for opioid medications for pain
  • Anticipated surgical procedure within 14-day of ED visit
  • Serologic evidence of liver disease (LFTs 3X normal) within 7 days of enrollment
  • Cirrhosis either by PMH or self-report
  • Pregnant or breastfeeding
  • Lacking contact information for follow-up
  • Requiring in-patient admission for medical or psychiatric reasons
  • Patient receiving a sexual assault forensics exam (SAFE)
  • Patient suspected of having COVID-19
  • Patient is actively suicidal or homicidal
  • Previously enrolled in either the implementation or feasibility phase of the study
  • Be a prisoner or in police custody at the time of the index ED visit
  • Be currently (anytime within the last 14 days) enrolled in formal addiction treatment, including by court order.

Sites / Locations

  • Mount Sinai Beth IsraelRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Oral Naloxone

Arm Description

Oral Naltrexone initiation

Outcomes

Primary Outcome Measures

Number of participants enrolled and receiving formal addiction treatment at day 14
Number of participant enrolled with engagement in care of comprehensive addiction treatment
Number of participants enrolled and receiving formal addiction treatment at day 30
Number of participant enrolled with engagement in care of comprehensive addiction treatment

Secondary Outcome Measures

Guidelines Regimen Information Program (GRIP) guide at day 14
Adherence to daily oral naltrexone measured using GRIP guide - GRIP guide is a self-report to assess adherence, with 6 categorical items: excellent, very good, good, fair, poor, and very poor.
Guidelines Regimen Information Program (GRIP) guide at day 30
Adherence to daily oral naltrexone measured using GRIP guide - GRIP guide is a self-report to assess adherence, with 6 categorical items: excellent, very good, good, fair, poor, and very poor.
Number of pills in bottle at day 14
Adherence to daily oral naltrexone measured using pill counts.
Number of pills in bottle at day 30
Adherence to daily oral naltrexone measured using pill counts.
Number of drinks
Daily alcohol intake self reported via a text-messaging application
Number of Heavy Drinking Days
Number of heavy drinking days defined as 4 or more drinks for a woman or 5 or more drinks for a man on the same occasion in a 24 hour period.
Health Services Utilization Survey
A brief, structured measure (not scored) regarding health care utilization (inpatient and outpatient) will be used, which collects information on the type and amount of services received. This includes ED visits, hospitalizations, primary medical care visits.
Number of participants who Transition to LA Injectable
Number of participants who transition from oral to long acting injectable naloxone.
Health Related Quality of Life (HRQoL)
HRQoL - full scale score ranges from 0 to 100, higher score indicates better health outcomes
The Patient Rated Inventory of Side Effects (PRISE) survey
Medication side effects of oral naltrexone measured using PRISE survey - is a patient self-report measure used to identify and evaluate the tolerability of side effect symptom. This scale is a 7 item assessment of the side effects in the following symptom areas; gastrointestinal, heart, skin, nervous system, eyes/ears, genital/urinary, sleep, sexual functioning, and other. Each domain has multiple symptoms and for each domain the patient rates whether these symptoms are tolerable or distressing. Higher score represents more side-effects.
Daily alcohol craving scale
Daily alcohol craving scale using Qualtrics - Full scale from 0 to 36, higher score represents more severity.
AUD Program Satisfaction Survey
Satisfaction with the naloxone initiation program measured using Satisfaction survey - full scale from 0 to 36 higher score represents more satisfaction.

Full Information

First Posted
March 23, 2021
Last Updated
March 7, 2023
Sponsor
Icahn School of Medicine at Mount Sinai
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1. Study Identification

Unique Protocol Identification Number
NCT04817410
Brief Title
ED Initiated Oral Naltrexone for AUD
Official Title
Emergency Department Initiated Oral Naltrexone for Patients With Moderate to Severe Alcohol Use Disorder: A Pilot Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 28, 2021 (Actual)
Primary Completion Date
April 2024 (Anticipated)
Study Completion Date
May 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Icahn School of Medicine at Mount Sinai

4. Oversight

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

5. Study Description

Brief Summary
This study will recruit Emergency Department (ED) patients with moderate to severe alcohol use disorder (AUD) who are interested in initiating medication assisted treatment (MAT). The study is split into two phases. The first phase (N=10) will use implementation science strategies to strengthen existing non-targeted ED based AUD screening program and optimize feasibility, acceptability, and linkage pathways. The second phase (N=20) will incorporate lessons learned from phase 1 to initiate ED patients on MAT for AUD in the form of oral naltrexone. The primary outcome for both phase 1 and phase 2 is engagement in comprehensive addiction treatment at 14 and 30 days post enrollment.
Detailed Description
Overview The study will be comprised of two components outlined below: Site Implementation Component In this component implementation science strategies will be used to strengthen existing non-targeted ED based AUD screening program and optimize feasibility, acceptability and linkage pathways. Three specific aims are to, 1) optimize registered nurse (RN) driven non-targeted alcohol use screening supplemented with secondary screening using DSM-5 criteria for AUD and an SBIRT (screening, brief intervention and referral to treatment) intervention administered by trained staff. 2) During a 3-month period, use continuous quality improvement methods to decrease the time for completion of AUD screening to an interval that is acceptable to ED patients and ED providers and 3) Assess willingness to initiate oral naltrexone among ED patients with moderate to severe AUD. Ten (10) patients will be enrolled in phase 1. Oral Naltrexone Feasibility Component In this component the study team aims to assess the feasibility of initiating treatment in ED patients with moderate to severe AUD on oral naltrexone, an evidence based and accepted standard of care treatment for AUD. Specifically, 1) over an 8-month period the study team aims to identify 20 patients with moderate to severe AUD eligible and interested in immediate initiation of oral naltrexone. Consenting patients will be receive a standard SBIRT intervention and be provided with immediate oral naltrexone initiation in the ED with a 14-day starter pack at the time of ED discharge. All participants will receive facilitated linkage to comprehensive out-patient care. 2) The study team aims will evaluate the impact of immediate ED initiated oral naltrexone with the primary outcome being engagement in comprehensive addiction care at 14 and 30 days post enrollment. Secondary outcomes include medication adherence, changes in daily alcohol consumption, number of heavy drinking days, hospital admissions and ED utilization, transition to long-acting injectable naltrexone and alcohol craving. 3) Lastly, the study team will collect data on recruitment and attrition rates, as well as means and standard deviations for key measures that will be needed to plan a definitive randomized controlled trial of ED-initiated oral naltrexone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Use Disorder
Keywords
Medication Assisted Treatment, Emergency Department, Naltrexone

7. Study Design

Primary Purpose
Screening
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Oral Naloxone
Arm Type
Experimental
Arm Description
Oral Naltrexone initiation
Intervention Type
Drug
Intervention Name(s)
Emergency Department Initiated Oral Naltrexone
Intervention Description
Emergency Department Initiated Oral Naltrexone
Primary Outcome Measure Information:
Title
Number of participants enrolled and receiving formal addiction treatment at day 14
Description
Number of participant enrolled with engagement in care of comprehensive addiction treatment
Time Frame
Day 14
Title
Number of participants enrolled and receiving formal addiction treatment at day 30
Description
Number of participant enrolled with engagement in care of comprehensive addiction treatment
Time Frame
Day 30
Secondary Outcome Measure Information:
Title
Guidelines Regimen Information Program (GRIP) guide at day 14
Description
Adherence to daily oral naltrexone measured using GRIP guide - GRIP guide is a self-report to assess adherence, with 6 categorical items: excellent, very good, good, fair, poor, and very poor.
Time Frame
Day 14
Title
Guidelines Regimen Information Program (GRIP) guide at day 30
Description
Adherence to daily oral naltrexone measured using GRIP guide - GRIP guide is a self-report to assess adherence, with 6 categorical items: excellent, very good, good, fair, poor, and very poor.
Time Frame
Day 30
Title
Number of pills in bottle at day 14
Description
Adherence to daily oral naltrexone measured using pill counts.
Time Frame
Day 14
Title
Number of pills in bottle at day 30
Description
Adherence to daily oral naltrexone measured using pill counts.
Time Frame
Day 30
Title
Number of drinks
Description
Daily alcohol intake self reported via a text-messaging application
Time Frame
up to 30 days
Title
Number of Heavy Drinking Days
Description
Number of heavy drinking days defined as 4 or more drinks for a woman or 5 or more drinks for a man on the same occasion in a 24 hour period.
Time Frame
up to 30 days
Title
Health Services Utilization Survey
Description
A brief, structured measure (not scored) regarding health care utilization (inpatient and outpatient) will be used, which collects information on the type and amount of services received. This includes ED visits, hospitalizations, primary medical care visits.
Time Frame
Day 30
Title
Number of participants who Transition to LA Injectable
Description
Number of participants who transition from oral to long acting injectable naloxone.
Time Frame
Day 30
Title
Health Related Quality of Life (HRQoL)
Description
HRQoL - full scale score ranges from 0 to 100, higher score indicates better health outcomes
Time Frame
Day 30
Title
The Patient Rated Inventory of Side Effects (PRISE) survey
Description
Medication side effects of oral naltrexone measured using PRISE survey - is a patient self-report measure used to identify and evaluate the tolerability of side effect symptom. This scale is a 7 item assessment of the side effects in the following symptom areas; gastrointestinal, heart, skin, nervous system, eyes/ears, genital/urinary, sleep, sexual functioning, and other. Each domain has multiple symptoms and for each domain the patient rates whether these symptoms are tolerable or distressing. Higher score represents more side-effects.
Time Frame
Day 30
Title
Daily alcohol craving scale
Description
Daily alcohol craving scale using Qualtrics - Full scale from 0 to 36, higher score represents more severity.
Time Frame
up to 30 days
Title
AUD Program Satisfaction Survey
Description
Satisfaction with the naloxone initiation program measured using Satisfaction survey - full scale from 0 to 36 higher score represents more satisfaction.
Time Frame
Day 30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Emergency Department patients 18 years of age or older Treated in the ED during screening hours Moderate to severe AUD as determined by DSM-5 criteria Able to speak and understand English Medically stable for an interview as determined by their primary ED provider Willing and able to consent to study participation Two points of contact available for follow-up Exclusion Criteria: ED patients younger than 18 years of age Medically or psychiatrically unstable as determined by the ED provider Unable to speak or understand English Unable to provide consent for study participation Past year opioid dependence Urine drug screen positive for opioids Current or anticipated need for opioid medications for pain Anticipated surgical procedure within 14-day of ED visit Serologic evidence of liver disease (LFTs 3X normal) within 7 days of enrollment Cirrhosis either by PMH or self-report Pregnant or breastfeeding Lacking contact information for follow-up Requiring in-patient admission for medical or psychiatric reasons Patient receiving a sexual assault forensics exam (SAFE) Patient suspected of having COVID-19 Patient is actively suicidal or homicidal Previously enrolled in either the implementation or feasibility phase of the study Be a prisoner or in police custody at the time of the index ED visit Be currently (anytime within the last 14 days) enrolled in formal addiction treatment, including by court order.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ethan Cowan, MD
Phone
212-420-2652
Email
ethan.cowan@mountsinai.org
First Name & Middle Initial & Last Name or Official Title & Degree
Lauren Gordon, MPH
Email
lauren.gordon@mountsinai.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ethan Cowan, MD
Organizational Affiliation
Icahn School of Medicine at Mount Sinai
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mount Sinai Beth Israel
City
New York
State/Province
New York
ZIP/Postal Code
10003
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ethan Cowan, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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ED Initiated Oral Naltrexone for AUD

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