- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01113190
Healthier You: Optimizing Screening, Brief Interventions, and Referral to Treatment (SBIRT) in the Emergency Department
April 6, 2016 updated by: Frederic C. Blow, University of Michigan
Optimizing SBIRT for Drug-Using Patients in an Inner-City Emergency Department
Screening, brief interventions, and referral to treatment (SBIRT) for drug use/abuse offers opportunities for early detection, brief intervention/treatment, and substance use treatment referrals for patients in medical settings.
Although SBIRT components, particularly screening and brief interventions, have been shown to be effective strategies for addressing alcohol misuse in primary care, data are limited on using all of the components of SBIRT for drug-using patients, particularly in the Emergency Department (ED).
Further, because of the often chaotic environment of EDs, many logistical and practical impediments exist for the adoption of the entire SBIRT model in this setting.
Study Overview
Status
Completed
Conditions
Detailed Description
The proposed study will use computerized screening using touch screen computer tablets with audio (~4,900 patients) and will test intervention strategies in a two-factorial design (3x2).
Specifically, 900 patients aged 18-60 in an inner-city ED who screen positive for drug use in the past 3 months will be randomized to the combinations of three ED-based conditions (computer brief intervention-CBI; intervener brief intervention-IBI; enhanced usual care-EUC), and two follow-up conditions (adapted motivational enhancement therapy-AMET; enhanced usual care-EUC) that will take place 3 months post-ED.
All individuals who meet criteria for a drug use disorder will additionally receive the "referral to treatment" or "RT" component of SBIRT.
Stratified random assignment [by gender and diagnosis of a drug use disorder (yes/no)] will take place at baseline for all ED based and follow-up conditions.
All participants will receive written information including substance abuse and other community resources, and HIV prevention materials.
Recognizing that brief interventions are important, but not necessarily sufficient, for change in all patients who use drugs, the primary specific aims of the proposed study will determine the independent effectiveness of immediate "on-the-spot" ED-based brief intervention conditions, 3-month followup brief treatment conditions, and combinations of conditions, for decreasing drug use and improving health-related outcomes (including physical and mental health, and HIV risk behavior) at 6 and 12 months.
Study Type
Interventional
Enrollment (Actual)
878
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
-
-
Michigan
-
Flint, Michigan, United States, 48503
- Hurley Medical Center Emergency Department
-
-
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 to 60 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- patients age 18-60 years presenting to the HMC for medical care (except exclusions as noted below)
- ability to provide informed consent. Additional inclusion criteria for intervention: past 3-month use of illicit drugs or misuse of psychoactive prescription drugs
Exclusion Criteria:
- patients who do not understand English (less than 1% in our prior work) -
- prisoners
- patients classified by medical staff as "Level 1 trauma" (e.g., unconscious, intubated on respirators, in need of immediate lifesaving procedures such as surgery)
- patients deemed unable to provide informed consent as stated above (e.g., intoxication, mental incompetence)
- patients treated in the ED for suicide attempts or sexual assault
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: Health Services Research
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: CBI in ED with AMET at 3 months
computer-delivered brief intervention (CBI) at baseline with adapted motivational enhancement therapy-AMET at 3 months
|
The multimedia, interactive Computer BI (CBI) condition will be delivered using tablet computers.
The content and format will be easily negotiated by participants.
The proposed CBI condition will use actors with 'green screen' to deliver scripted therapist content that will be highly tailored to individual responses.
'Green screens' are standard recording formats that allow for inserting engaging background and other overlays onto recorded material.
This program will be viewed on a touch screen tablet computer with audio delivered via headphones.
The CBI will be designed in a therapist video-delivered interactive style, that provides tailoring options for reviewing patient goals, providing feedback regarding substance use patterns and consequences, completing a "decisional balance" exercise, and formulating a change plan.
It requires active participation and is not a passive video that is merely viewed.
This session will have a similar general outline to the sessions conducted in the ED, including a review of participants' goals and values, and a review of their substance use and consequences, use of decisional balance exercises as indicated, and review and modification of their change plan.
For the AMET intervention, the intervener (at least master's level) will conduct a single session (~30-45 minutes) in the community (HMC ED or our community research office).
The therapist will be able to tailor their approach to each individual's needs and motivational state.
|
|
Active Comparator: CBI in ED with EUC at 3 months
computer-delivered brief intervention (CBI) at baseline with enhanced usual care-EUC at 3 months
|
The multimedia, interactive Computer BI (CBI) condition will be delivered using tablet computers.
The content and format will be easily negotiated by participants.
The proposed CBI condition will use actors with 'green screen' to deliver scripted therapist content that will be highly tailored to individual responses.
'Green screens' are standard recording formats that allow for inserting engaging background and other overlays onto recorded material.
This program will be viewed on a touch screen tablet computer with audio delivered via headphones.
The CBI will be designed in a therapist video-delivered interactive style, that provides tailoring options for reviewing patient goals, providing feedback regarding substance use patterns and consequences, completing a "decisional balance" exercise, and formulating a change plan.
It requires active participation and is not a passive video that is merely viewed.
The EUC group will receive brief advice to change their drug use, as well as a booklet including information on community support groups, location of substance use treatment centers, mental health services, suicide prevention hotlines, risk of injecting drugs including HIV and hepatitis and HIV prevention and testing information.
|
|
Active Comparator: IBI in ED with AMET at 3 months
intervener-delivered brief intervention (IBI) at baseline with adapted motivational enhancement therapy-AMET at 3 months
|
This session will have a similar general outline to the sessions conducted in the ED, including a review of participants' goals and values, and a review of their substance use and consequences, use of decisional balance exercises as indicated, and review and modification of their change plan.
For the AMET intervention, the intervener (at least master's level) will conduct a single session (~30-45 minutes) in the community (HMC ED or our community research office).
The therapist will be able to tailor their approach to each individual's needs and motivational state.
IBI is a 30-minute intervention session with a master's-level clinician.
The interventions will include FRAMES (Miller & Rollnick, 2002): personalized Feedback (regarding substance use, risk factors), emphasis on Responsibility for change, Advice, Menu of options, Empathic clinical behaviors, and support of Self-Efficacy regarding making changes.
The interventions are designed to address the primary target behavior of drug use, and will include a tailored review of participants' goals/values, feedback regarding their present substance use patterns and consequences, developing a discrepancy between their substance use and ability to meet goals and values through a decisional balance exercise, and formulation of a "change plan" tailored for each participant.
IBI will be highly individualized to participants' goals, values and substance use, and will will follow similar session outlines and length of delivery as the CBI sessions.
|
|
Active Comparator: IBI in ED with EUC at 3 months
intervener-delivered brief intervention (IBI) at baseline with enhanced usual care-EUC at 3 months
|
The EUC group will receive brief advice to change their drug use, as well as a booklet including information on community support groups, location of substance use treatment centers, mental health services, suicide prevention hotlines, risk of injecting drugs including HIV and hepatitis and HIV prevention and testing information.
IBI is a 30-minute intervention session with a master's-level clinician.
The interventions will include FRAMES (Miller & Rollnick, 2002): personalized Feedback (regarding substance use, risk factors), emphasis on Responsibility for change, Advice, Menu of options, Empathic clinical behaviors, and support of Self-Efficacy regarding making changes.
The interventions are designed to address the primary target behavior of drug use, and will include a tailored review of participants' goals/values, feedback regarding their present substance use patterns and consequences, developing a discrepancy between their substance use and ability to meet goals and values through a decisional balance exercise, and formulation of a "change plan" tailored for each participant.
IBI will be highly individualized to participants' goals, values and substance use, and will will follow similar session outlines and length of delivery as the CBI sessions.
|
|
Active Comparator: EUC in ED with AMET at 3 months
enhanced usual care (EUC) at baseline with adapted motivational enhancement therapy-AMET at 3 months
|
This session will have a similar general outline to the sessions conducted in the ED, including a review of participants' goals and values, and a review of their substance use and consequences, use of decisional balance exercises as indicated, and review and modification of their change plan.
For the AMET intervention, the intervener (at least master's level) will conduct a single session (~30-45 minutes) in the community (HMC ED or our community research office).
The therapist will be able to tailor their approach to each individual's needs and motivational state.
The EUC group will receive brief advice to change their drug use, as well as a booklet including information on community support groups, location of substance use treatment centers, mental health services, suicide prevention hotlines, risk of injecting drugs including HIV and hepatitis and HIV prevention and testing information.
|
|
Active Comparator: EUC in ED with EUC at 3 months
enhanced usual care (EUC) at baseline with EUC at 3 months
|
The EUC group will receive brief advice to change their drug use, as well as a booklet including information on community support groups, location of substance use treatment centers, mental health services, suicide prevention hotlines, risk of injecting drugs including HIV and hepatitis and HIV prevention and testing information.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
drug use
Time Frame: change over time (3, 6 and 12 months post-baseline)
|
Drug use is measured using the NIDA-Modified ASSIST (Alcohol, Smoking and Substance Involvement Screening Test).
|
change over time (3, 6 and 12 months post-baseline)
|
|
drug use - number of days used
Time Frame: change over time (3, 6 and 12 months post-baseline)
|
change over time (3, 6 and 12 months post-baseline)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
HIV risk behaviors
Time Frame: change over time (3, 6 and 12 months post-baseline)
|
HIV risk behaviors are measured using the Health Related Behavior Survey (HRBS).
|
change over time (3, 6 and 12 months post-baseline)
|
|
health related outcomes (physical health)
Time Frame: change over time (3, 6 and 12 months post-baseline)
|
Physical health is measured using the Short Form Health Survey (SF-12).
|
change over time (3, 6 and 12 months post-baseline)
|
|
health related outcomes (mental health)
Time Frame: change over time (3, 6 and 12 months post-baseline)
|
Mental health is measured using the Brief Symptom Inventory (BSI-18).
|
change over time (3, 6 and 12 months post-baseline)
|
|
health related outcomes (mental health)
Time Frame: change over time (3, 6 and 12 months post-baseline)
|
Mental health is measured using the Patient Health Questionnaire (PHQ-9).
|
change over time (3, 6 and 12 months post-baseline)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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
February 1, 2011
Primary Completion (Actual)
March 1, 2014
Study Completion (Actual)
March 1, 2014
Study Registration Dates
First Submitted
April 20, 2010
First Submitted That Met QC Criteria
April 27, 2010
First Posted (Estimate)
April 29, 2010
Study Record Updates
Last Update Posted (Estimate)
April 7, 2016
Last Update Submitted That Met QC Criteria
April 6, 2016
Last Verified
April 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- DA026029
- R01DA026029 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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