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A Hybrid Effectiveness Implementation Study of Latino/a Alcohol and Drug Users (CAMI-HI)

Primary Purpose

Alcohol Use Disorder, Drug Use, Psychological Distress

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CAMI
Sponsored by
Boston University Charles River Campus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alcohol Use Disorder focused on measuring Alcohol, Drug, Latinx, Treatment, Psychological distress

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 4/5 or more drinks/occasion (female/male, respectively) 1+ days/month AND/OR AUDIT score of 8+ for men and 6+ for women
  • Age 18 or older
  • Identify as Latinx
  • First or second-generation immigrants

Exclusion Criteria:

  • Current psychotic symptoms
  • Cognitive impairment
  • Currently in psychosocial treatment for alcohol use disorder
  • Patients who have been enrolled in the Complex Care Management (CCM) Program for 3 months or longer.

Sites / Locations

  • Boston Medical CenterRecruiting
  • Mercy Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

CAMI/CAMI booster

Control

Arm Description

Culturally Adapted Motivational Interview. Participants will receive a single session, 75 minute addiction counseling discussion that focuses on the causes of addictive behavior. They will receive a CAMI booster session at 2 months and standard care in a primary care setting.

Assessment plus standard care. Participants will complete an assessment, including measures on drinking and drug use. They will also receive standard care in a primary care setting.

Outcomes

Primary Outcome Measures

Percent heavy drinking days
% heavy drinking days (4 or 5 drinks/day female/male, respectively)
Alcohol-related consequences
Frequency of alcohol related consequences (e.g., driving under the influence).
Percent drug use days
% drug use days

Secondary Outcome Measures

Percent heavy drinking days
% heavy drinking days (4 or 5 drinks/day female/male, respectively)
Percent heavy drinking days
% heavy drinking days (4 or 5 drinks/day female/male, respectively)
Alcohol-related consequences
Frequency of alcohol related consequences (e.g., driving under the influence).
Alcohol-related consequences
Frequency of alcohol related consequences (e.g., driving under the influence).
Center for Epidemiological Studies - Depression
Level of depressive symptomatology in the past week.
Center for Epidemiological Studies - Depression
Level of depressive symptomatology in the past week.
Center for Epidemiological Studies - Depression
Level of depressive symptomatology in the past week.
Beck Anxiety Inventory
Level of anxiety symptomatology in the past week.
Beck Anxiety Inventory
Level of anxiety symptomatology in the past week.
Beck Anxiety Inventory
Level of anxiety symptomatology in the past week.
Percent drug use days
% drug use days
Percent drug use days
% drug use days

Full Information

First Posted
February 11, 2021
Last Updated
September 22, 2023
Sponsor
Boston University Charles River Campus
Collaborators
Brown University, National Institutes of Health (NIH), National Institute on Alcohol Abuse and Alcoholism (NIAAA)
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1. Study Identification

Unique Protocol Identification Number
NCT04771650
Brief Title
A Hybrid Effectiveness Implementation Study of Latino/a Alcohol and Drug Users
Acronym
CAMI-HI
Official Title
Addressing Alcohol-Use Related Health Disparities: A Hybrid Effectiveness Implementation Study of a Culturally Adapted MI for Latino/a Alcohol and Drug Users
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 25, 2022 (Actual)
Primary Completion Date
April 25, 2027 (Anticipated)
Study Completion Date
August 1, 2028 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boston University Charles River Campus
Collaborators
Brown University, National Institutes of Health (NIH), National Institute on Alcohol Abuse and Alcoholism (NIAAA)

4. Oversight

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

5. Study Description

Brief Summary
Alcohol use is a significant problem among Latinxs and immigration-related stress increases risk for substance use. A theoretically-based cultural adaptation of motivational interviewing (CAMI) that specifically integrated discussion of immigration-related stressors (e.g., stigma, social isolation) resulted in significant reductions in alcohol-related harms for those Latinx heavy drinkers with high discrimination compared to standard MI, and reduced anxiety and depressive symptoms one year later compared to MI. Rigorous tests that examine theoretically-informed adaptation of efficacious addiction interventions are not common, yet are needed to advance implementation science. This Hybrid Type 1 Effectiveness-Implementation study will investigate the feasibility of implementing CAMI in a real-world clinical setting. The key questions are: Would CAMI have positive effects among individuals who use both drugs and alcohol? How do providers view this intervention? The investigators will collaborate with a primary care center that serves a mainly Latinx client population to train their Community Wellness Advocates (CWAs) to deliver CAMI to patients who are heavy drinkers. The investigators will conduct a concurrent investigation on the process of implementing CAMI in primary care - a two-arm randomized clinical effectiveness trial will enroll Latinx heavy drinkers (18 years or older) in primary care who use alcohol (and may use other drugs) - and follow them for 12 months after the intervention. Specific Aims are: (1) To examine the impact of CAMI plus a booster session (vs. assessment only) on outcomes: % heavy drinking days, frequency of alcohol-related consequences, depressive/anxiety symptoms, and number of illicit drug use days, using a Hybrid Type 1 Effectiveness-Implementation design and (2) To gather indicators of implementation outcome from multiple stakeholders using a mixed-methods approach. The investigators will follow Curran's framework to evaluate the process of implementation and Proctor's framework to measure implementation outcomes. This study, a first to examine the acceptability of culturally-adapted addiction treatments in primary care settings, will answer essential questions on implementing evidence-based care for Latinxs that can improve health disparities related to substance use. Long term goals are to translate the lessons from this Hybrid study to the broader community to focus on population health for all primary care patients.
Detailed Description
Alcohol use is a significant problem among Latinxs because of the disproportionate burden of physical harms and negative consequences associated with substance use relative to other racial/ethnic groups. Factors associated with the stress related to being an immigrant increase risk for substance use. A theoretically-based cultural adaptation of motivational interviewing (CAMI) that specifically integrated discussion of stressors related to immigration (e.g., discrimination, stigma, social isolation) resulted in significant reductions in harms related to alcohol for those Latinx heavy drinkers with high discrimination compared to standard MI, and reduced anxiety and depressive symptoms one year later compared to MI. Rigorous tests that examine theoretically-informed adaptation of efficacious interventions for addictions are not common, yet are needed to advance implementation science because they address questions that are the basis for successful implementation. The proposed Hybrid Type 1 Effectiveness-Implementation study is an important next step in this line of research, which is to investigate the feasibility of implementing the CAMI intervention in a real-world clinical setting. The key questions are: Would CAMI have positive effects among individuals who use both drugs and alcohol? How do providers view this intervention? The investigators will collaborate with a primary care center that serves a mainly Latinx client population to train their Community Wellness Advocates (CWAs) to deliver the CAMI to patients who are heavy drinkers. The investigators will conduct a concurrent investigation on the process of implementing the CAMI in primary care - a two-arm randomized clinical effectiveness trial will enroll Latinx heavy drinkers (18 years or older) in primary care who use alcohol (and may use other drugs) - and follow them for 12 months after the intervention. Specific Aims are: (1) To examine the impact of CAMI plus an in- person booster session (vs. assessment only) on outcomes: % heavy drinking days, frequency of alcohol- related consequences, depressive/anxiety symptoms, and number of illicit drug use days, using a Hybrid Type 1 Effectiveness-Implementation design and (2) To gather indicators of implementation outcome from multiple stakeholders using a mixed-methods approach. The investigators will follow Curran's framework to evaluate the process of implementation and Proctor's framework to measure implementation outcomes: acceptability, adoption, intervention appropriateness, feasibility, overall cost (i.e., CAMI vs. assessment only), and treatment fidelity. This study, a first to examine the acceptability of culturally-adapted addiction treatments in primary care settings, will answer essential questions on implementing evidence-based care for Latinxs that can improve health disparities related to substance use. Long term goals are to translate the lessons from the proposed Hybrid study to the broader community to focus on population health for all primary care patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Use Disorder, Drug Use, Psychological Distress
Keywords
Alcohol, Drug, Latinx, Treatment, Psychological distress

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Clinical effectiveness trial that tests two conditions (CAMI plus booster + standard care compared to assessment + standard care). Health outcomes are reduced drinking, related harms and improvement of mental health. Follow-up at 3,6, and 12 months.
Masking
ParticipantOutcomes Assessor
Masking Description
Participants will be randomized to one of two conditions. They will be unaware of their randomization condition. The Research assistant conducting follow-ups will be unaware of the participant's treatment condition.
Allocation
Randomized
Enrollment
220 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CAMI/CAMI booster
Arm Type
Experimental
Arm Description
Culturally Adapted Motivational Interview. Participants will receive a single session, 75 minute addiction counseling discussion that focuses on the causes of addictive behavior. They will receive a CAMI booster session at 2 months and standard care in a primary care setting.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Assessment plus standard care. Participants will complete an assessment, including measures on drinking and drug use. They will also receive standard care in a primary care setting.
Intervention Type
Other
Intervention Name(s)
CAMI
Intervention Description
The CAMI is a culturally adapted motivational interview. It is a single 75 minute session that focuses on promoting motivation to change drinking and drug use behavior.
Primary Outcome Measure Information:
Title
Percent heavy drinking days
Description
% heavy drinking days (4 or 5 drinks/day female/male, respectively)
Time Frame
3 month follow-up
Title
Alcohol-related consequences
Description
Frequency of alcohol related consequences (e.g., driving under the influence).
Time Frame
3 month follow-up
Title
Percent drug use days
Description
% drug use days
Time Frame
3 month follow-up
Secondary Outcome Measure Information:
Title
Percent heavy drinking days
Description
% heavy drinking days (4 or 5 drinks/day female/male, respectively)
Time Frame
6 month follow-up
Title
Percent heavy drinking days
Description
% heavy drinking days (4 or 5 drinks/day female/male, respectively)
Time Frame
12 month follow-up
Title
Alcohol-related consequences
Description
Frequency of alcohol related consequences (e.g., driving under the influence).
Time Frame
6 month follow-up
Title
Alcohol-related consequences
Description
Frequency of alcohol related consequences (e.g., driving under the influence).
Time Frame
12 month follow-up
Title
Center for Epidemiological Studies - Depression
Description
Level of depressive symptomatology in the past week.
Time Frame
3 month follow-up
Title
Center for Epidemiological Studies - Depression
Description
Level of depressive symptomatology in the past week.
Time Frame
6 month follow-up
Title
Center for Epidemiological Studies - Depression
Description
Level of depressive symptomatology in the past week.
Time Frame
12 month follow-up
Title
Beck Anxiety Inventory
Description
Level of anxiety symptomatology in the past week.
Time Frame
3 month follow-up
Title
Beck Anxiety Inventory
Description
Level of anxiety symptomatology in the past week.
Time Frame
6 month follow-up
Title
Beck Anxiety Inventory
Description
Level of anxiety symptomatology in the past week.
Time Frame
12 month follow-up
Title
Percent drug use days
Description
% drug use days
Time Frame
6 month follow-up
Title
Percent drug use days
Description
% drug use days
Time Frame
12 month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Meets criteria for binge drinking in the past month (> 4/5 (females/males) drinks/occasion, 1+ days/month) Age 18 or older Identify as Latinx First or second-generation immigrant Exclusion Criteria: Current psychotic symptoms Cognitive impairment Currently in psychosocial treatment for alcohol use disorder Patients who have been enrolled in the Complex Care Management (CCM) before January 1, 2021.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Christina S Lee, PhD
Phone
617 353 1415
Email
leecs@bu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christina S Lee, PhD
Organizational Affiliation
Boston University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Boston Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christine Pace, MD
Email
CHRISTINE.PACE@BMC.ORG
Facility Name
Mercy Medical Center
City
Springfield
State/Province
Massachusetts
ZIP/Postal Code
01104
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ari Kriegsman, MD
Email
Ari.Kriegsman@trinityhealthofne.org

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27565832
Citation
Lee CS, Colby SM, Magill M, Almeida J, Tavares T, Rohsenow DJ. A randomized controlled trial of culturally adapted motivational interviewing for Hispanic heavy drinkers: Theory of adaptation and study protocol. Contemp Clin Trials. 2016 Sep;50:193-200. doi: 10.1016/j.cct.2016.08.013. Epub 2016 Aug 24.
Results Reference
background
PubMed Identifier
31403817
Citation
Lee CS, Colby SM, Rohsenow DJ, Martin R, Rosales R, McCallum TT, Falcon L, Almeida J, Cortes DE. A randomized controlled trial of motivational interviewing tailored for heavy drinking latinxs. J Consult Clin Psychol. 2019 Sep;87(9):815-830. doi: 10.1037/ccp0000428.
Results Reference
background

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A Hybrid Effectiveness Implementation Study of Latino/a Alcohol and Drug Users

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