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Motivational Interviewing for Substance Use Disorders
N/A
Recruiting
Led By Margo Hurlocker, PhD
Research Sponsored by University of New Mexico
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline and 1 year
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing if a special way of talking to patients when they start addiction treatment can help them stay engaged. The method involves counselors helping patients find their own reasons for wanting to change.
Who is the study for?
This trial is for English-speaking adults seeking outpatient treatment for alcohol or drug use, who are willing to follow study procedures and have given informed consent. It's also open to staff at the treatment programs. Participants must not be physically dependent on substances at the time of intake.
What is being tested?
The study compares two approaches: usual intake procedures versus Motivational Interviewing at Intake (MII) to see which is more effective in engaging clients in addiction treatment. The trial will also assess how easy it is to integrate MII into regular practice.
What are the potential side effects?
Since this trial involves counseling techniques rather than medication, traditional side effects are not expected. However, participants may experience emotional discomfort discussing their substance use during motivational interviewing sessions.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline and 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and 1 year
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Number of participants who attended the first outpatient treatment program session based on electronic medical record review
Number of participants who completed the three-month outpatient treatment program based on electronic medical record review
Number of treatment sessions attended during the three-month outpatient treatment program based on electronic medical record review
Secondary study objectives
Change from baseline in client readiness to enter treatment on the University of Rhode Island Change Assessment Scale (URICA) at 1 hour post-intake
Score on therapeutic alliance on the Working Alliance Inventory (WAI) at 1-hour post-intake
Other study objectives
Change from baseline in organizational capability to change on the Change Process Capability Questionnaire (CPCQ) at Year 1
Change from baseline in organizational readiness to change on the Readiness for Organizational Change (ROC) at 1 year
Change from baseline in organizational readiness to change on the Texas Christian University-Organizational Readiness to Change (TCU-ORC) at 1 year
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Motivational Interviewing at Intake (MII)Experimental Treatment1 Intervention
Clients allocated to the MII condition will receive a 90-minute pure Motivational Interviewing (MI) session.
Group II: Intake as Usual (IAU)Active Control1 Intervention
Clients allocated to the IAU condition will receive the 90-minute standard assessment that is delivered to all clients entering intensive outpatient program (IOP)/outpatient program (OP).
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Substance Use Disorders (SUDs) include Cognitive Behavioral Therapy (CBT), Motivational Interviewing (MI), and Contingency Management (CM). CBT helps patients identify and modify distorted thinking patterns and behaviors that contribute to substance use, promoting healthier coping strategies.
MI enhances client engagement by addressing ambivalence and fostering intrinsic motivation for change, making it particularly effective at the intake stage. CM uses positive reinforcement, such as vouchers or rewards, to encourage abstinence and adherence to treatment.
These mechanisms are crucial as they address the psychological and behavioral aspects of addiction, improving treatment retention and outcomes for SUD patients.
Self-awareness deficits associated with lower treatment motivation in cocaine addiction.A review of psychosocial interventions for amphetamine use.
Self-awareness deficits associated with lower treatment motivation in cocaine addiction.A review of psychosocial interventions for amphetamine use.
Find a Location
Who is running the clinical trial?
National Institute on Drug Abuse (NIDA)NIH
2,587 Previous Clinical Trials
3,328,398 Total Patients Enrolled
University of New MexicoLead Sponsor
386 Previous Clinical Trials
3,525,924 Total Patients Enrolled
Margo Hurlocker, PhDPrincipal InvestigatorUniversity of New Mexico
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am not experiencing severe mental health issues like psychosis, mania, or suicidal thoughts.I am an adult who speaks English and am seeking treatment for substance use.You need to give your consent electronically.I speak English and work at an outpatient addiction treatment center.You are willing to follow all the study procedures.You have signed a document that says you understand and agree to participate in the study.You have stopped using alcohol or drugs.
Research Study Groups:
This trial has the following groups:- Group 1: Intake as Usual (IAU)
- Group 2: Motivational Interviewing at Intake (MII)
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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