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Linking Individuals Needing Care for Substance Use Disorders to Peer Coaches

Not Applicable
Recruiting
Conditions
Substance Use Disorders
Interventions
Behavioral: Peer recovery coaching with linkage to recovery resources
Behavioral: Usual Care
Registration Number
NCT05847621
Lead Sponsor
Emory University
Brief Summary

This is a 3-arm randomized controlled trial. Participants will be randomized via a maximally tolerated imbalance randomization procedure using NCI's Clinical Trial Randomization Tool with 1:1:1 allocation to each group: in-person peer recovery coaching (PRC) with linkage to recovery resources, telemedicine-based peer recovery coaching with linkage to recovery resources, or usual care.

In the PRC arms, PRCs will meet patients at bedside (in person) or via a tablet-based video call (telemedicine). They will assess the participant's state of change, engage in motivational interviewing techniques, and link the participant to community-based recovery resources according to the needs of the participant. They will also schedule and perform follow up calls after the participant is discharged from the ED to provide ongoing support and facilitate re-linkage to recovery resources, if needed.

Participants in the usual care arm will be provided with a list of community recovery resources, but there will be no PRC interaction or direct linkage to resources through the study.

Follow up visits will take place at 7, 30, and 90 days after enrollment. Most will take place via telephone, but participants will be given the option of an in-person visit if they so desire.

Detailed Description

Deaths from drug overdose have risen to record levels since the onset of the COVID-19 pandemic, disproportionately impacting Black individuals and people experiencing homelessness. Fewer than one-third of the 8.3 million individuals living with an illicit drug use disorder in 2019 reported receiving treatment. Telemedicine services have increased access to care for many patients living with substance use disorders (SUD), but the long-term role of this treatment approach in SUD care is uncertain. Multifaceted strategies are needed to build recovery capital and link vulnerable individuals to recovery resources.

Emergency department (ED) visits are an opportunity to screen for SUDs, initiate treatment, and link to recovery resources. Observational studies have noted that consultation with a peer recovery coach (PRC) was well-received in EDs, with high rates of engagement and satisfaction. PRCs facilitate conversations allowing patients to express their ideal pathway to recovery, provide linkage to services across the social ecology, and follow up to support recovery, including re-linkage to resources as needed. Nonetheless, their role in ED screening and linkage to resources, including the potential role of telemedicine, has not been rigorously evaluated.

The investigators will conduct a randomized controlled trial enrolling 600 subjects across three arms: in-person peer coaching with linkage to recovery support services and callbacks, telemedicine-based peer coaching with linkage and callbacks, or usual care. Results will inform other EDs considering a peer recovery coach program for patients presenting with SUD-related conditions. By utilizing telemedicine, this model will be rapidly scalable and readily implemented at other facilities.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
600
Inclusion Criteria
  1. ED patient or hospitalized through the ED within last 24 hours
  2. Age 18 years or older
  3. Able to speak and understand English
  4. Clinically sober, able to provide informed consent
  5. Score of 3 or greater - "moderate level", "substantial level", or "severe level" of problems related to drug abuse - on Drug Abuse Screening Test (DAST-10).(103, 104)
  6. Willing to follow study procedures and complete research follow-up calls
  7. Have at least one reliable contact number
Exclusion Criteria
  1. Medically or psychiatrically unstable as determined by treating physician
  2. Prisoner or in police custody
  3. Prior participation in the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
In-person peer recovery coaching with linkage to recovery resourcesPeer recovery coaching with linkage to recovery resourcesPRCs will meet patients at bedside (in person). They will also schedule and perform follow up calls after the participant is discharged from the ED to provide ongoing support and facilitate re-linkage to recovery resources, if needed. Follow-up data collection on day 7, 30, 90 post discharge.
Telemedicine-based peer recovery coaching with linkage to recovery resourcesPeer recovery coaching with linkage to recovery resourcesPRCs will meet patients via a tablet-based video call (telemedicine). They will also schedule and perform follow up calls after the participant is discharged from the ED to provide ongoing support and facilitate re-linkage to recovery resources, if needed. Follow-up data collection on day 7, 30, 90 post discharge.
Usual CareUsual CareParticipants in the usual care arm will be provided with a list of community recovery resources. No callbacks or re-linkage to recovery resources. Follow-up data collection on day 7, 30, 90 post discharge.
Primary Outcome Measures
NameTimeMethod
Change in number of participants with successful linkage to at least one recovery resourceBaseline, 30 and 90 days after enrollment

Change in number of participants with successful linkage to at least one recovery resource (formal addiction treatment, Recovery Community Organization (RCO), or harm reduction organization) at 30 days and 90 days after enrollment.

Secondary Outcome Measures
NameTimeMethod
Number of Emergency Department (ED) visits90 days post intervention

Number of ED visits will be collected

Number of hospitalizations90 days post intervention

Number of hospitalizations will be collected

Change in number of successful engagements with PRC after ED visitBaseline, 7, 30, and 90 days after enrollment

Change in number of successful engagements with PRC (peer recovery coach) after ED visit

Self-reported substance use in last 30 daysBaseline, 30 and 90 days post intervention

Self-reported substance use in last 30 days as measured by Timeline Follow-back (TLFB). It will be reported in number of episodes per day.

Change in number of episodes of re-linkage to recovery resourcesBaseline, 7, 30, and 90 days post intervention

Change in number of episodes of re-linkage to recovery resources

Number of nonfatal overdose events90 days post intervention

Number of nonfatal overdose events will be collected

Change in number of participants based on Housing statusBaseline, 7, 30, and 90 days post intervention

Housing status will be reported specifying one of the categories: apartment, Single family house, homeless, shelter, dormitory, multifamily house. Number of participants will be reported in each category at 0, 7, 30, 90 days post intervention.

Change in Brief Assessment of Recovery Capital (BARC-10)Baseline, 7, 30, and 90 days after enrollment

This outcome will be evaluated obtaining a score on a scale. The range of possible responses is 10-60. Higher score correlates with better outcome.

Number of fatal overdose events90 days post intervention

Number of fatal overdose events will be collected

Change in Social connections and isolation scoreBaseline, 7, 30, 90 days post intervention

Social isolation scores range from 0 to 4, with 0 representing the highest level of social isolation and 4 representing the lowest level.

Change in employment status90 days post intervention

Choices include: disabled, employed 32 hours or more per week, employed less than 32 hours per week, full-time student, homemaker, on medical leave, only temporarily laid off/sick leave/maternity leave, other, part-time student, retired, unemployed, and unknown. This outcome would measure a change in employment status from any of the choices to another one.

Trial Locations

Locations (1)

Grady Memorial Hospital

🇺🇸

Atlanta, Georgia, United States

Grady Memorial Hospital
🇺🇸Atlanta, Georgia, United States
Joseph Carpenter, MD
Principal Investigator
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