- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04248023
Screening and Management of Unhealthy Alcohol Use in Primary Care
July 21, 2023 updated by: Virginia Commonwealth University
Practice Facilitation to Promote Evidence-based Screening and Management of Unhealthy Alcohol Use in Primary Care
Unhealthy alcohol use is the third leading preventable cause of death in the United States.
Yet, primary care physicians do not, on average, screen for and address unhealthy alcohol use in their patient populations.
By implementing practice changes to promote screening and treatment, patients stand to reduce unhealthy alcohol use and benefit from improved health outcomes.
This project will provide a sample of Virginia primary care practices with a practice facilitator, practice specific resources, education on screening and counseling, and education on medication assisted therapy.
The project will measure whether this change will improve screening rates and promote reduction of unhealthy alcohol use.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Unhealthy alcohol use is the third leading cause of preventable death in the US.
Evidence shows that screening for unhealthy alcohol use and providing persons engaged in risky drinking with brief behavioral counseling interventions improves health outcomes, collectively termed screening and brief intervention (SBI).
For moderate or severe alcohol use disorder (AUD), medication assistance therapy (MAT) is effective.
Despite clear evidence of effectiveness, only 13% of primary care patients are screened with a standard instrument and only 6.7% of adults with AUD receive treatment.
We believe that underutilization of SBI and MAT are driven by both a misunderstanding of the role and effectiveness of primary care in addressing unhealthy alcohol and limited practice resource and infrastructure.
To promote the dissemination and implementation of evidence-based strategies to address unhealthy alcohol use throughout Virginia, we have extended our EvidenceNow collaboration to include addiction medicine experts at Virginia Commonwealth University, the Virginia Ambulatory Care Outcomes Research Network (ACORN), our state's family medicine residency training programs, and our state's Community Service Boards.
We propose a practice-level cluster randomized trial with wait list control.
125 primary care practices in five regions throughout the state, each centered around a residency site for educational support, will receive a practice facilitation intervention to implement screening, counseling, and treatment for unhealthy alcohol at intervention start or 6-month delay.
Guided by the identified EvidenceNow key drivers for change, practice support will include practice facilitation, education and training, shared learning and best practices, screening and counseling toolkits, data support, and assessment with feedback.
Each practice will identify a clinician, nurse, and administrator champion to locally lead efforts and participate in learning collaboratives.
Practices will design and implement screening, counseling, and treatment processes and operational changes, adapting their implementation strategy based on experiences and findings from other sites.
We will conduct a mixed methods analysis.
Primary outcomes will include the increase in screening for unhealthy alcohol use, increase in provision of brief counseling interventions and MAT, and reduction in alcohol intake for patients after practices receive practice facilitation.
We will use the consolidated framework for implementation research to code and rate practice facilitation (e.g.
dose, mode, reach) and practice implementation strategies (e.g.
SBI and MAT strategies and tools implemented) on outcomes.
Data sources will include practice facilitator field notes and interviews, chart reviews, patient survey, clinician survey, All Payer Claims Data, and qualitative interviews.
We will administer the patient survey at baseline, 3 months, and 6 months after the intervention.
Among patients age 18 to 75 with an office visit the prior month, we will randomly select 60 to survey.
In addition to our internal evaluation, we will participate in the external collaborative evaluation and dissemination activities with AHRQ throughout the project.
Study Type
Interventional
Enrollment (Actual)
13680
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Virginia
-
Richmond, Virginia, United States, 23298
- Virginia Commonwealth University
-
Richmond, Virginia, United States, 23298
- Virginia Ambulatory Care Outcomes Research Network
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Practice Inclusion Criteria:
- Primary care practices
- Ambulatory care practices
Patient Inclusion Criteria:
1. Patients 18 years and older and with an office visit at an included study site
Practice Exclusion Criteria:
- Practices that do not provide outpatient care
- Practices that do not provide primary care
Patient Exclusion Criteria:
- Patients under 18 years old
- Patients without an office visit
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention Practices
Intervention practices will work with a practice facilitator to make practice specific changes to address unhealthy alcohol use.
|
A practice facilitator will be assigned the each participating practice to assist with the development of a workflow, screening process, counseling resources, and referral resources for unhealthy alcohol use.
Practices in control group will receive delayed intervention at 3 months after their matched cohort of practices.
|
|
No Intervention: Control Practices
Control practices will continue to screening and address unhealthy alcohol use based on their existing practice patterns.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Screening for Unhealthy Alcohol Use
Time Frame: 6 months
|
This outcome will evaluate the percent of patients who were screened in clinic or report screening for alcohol use (numerator = intervention patients sampled who received counseling/ denominator = intervention patients who did not receive counseling at 3 time points.)
|
6 months
|
|
Treatment for Unhealthy Alcohol Use
Time Frame: 6 months
|
This outcome will measure the percent of patients, screening positive for risky alcohol use, that receive any type of treatment including, but not limited to, counseling, brief intervention, motivational interviewing, referral, or medication assisted treatment.
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Reduction of Unhealthy Alcohol Use
Time Frame: 6 months
|
This measure will identify the percent of patients with unhealthy alcohol use that have reduced alcohol intake after practice facilitation (numerator = number of sample patients with unhealthy alcohol use at baseline that received treatment / denominator = number of patients with unhealthy alcohol use at baseline.)
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Alexander H Krist, MD, MPH, Virginia Commonwealth University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 15, 2020
Primary Completion (Actual)
July 30, 2022
Study Completion (Actual)
May 31, 2023
Study Registration Dates
First Submitted
January 27, 2020
First Submitted That Met QC Criteria
January 29, 2020
First Posted (Actual)
January 30, 2020
Study Record Updates
Last Update Posted (Actual)
July 25, 2023
Last Update Submitted That Met QC Criteria
July 21, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HM20016728
- 1R18HS027077-01 (U.S. AHRQ Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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