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The goal of this clinical trial is to determine whether Emotional Brain Training (EBT), a behavioral modification method, can help manage stress and health problems related to addiction. EBT teaches skills to deactivate harmful circuits (automatic reactions) and activate healing circuits to quickly shift mood from negative to positive. Participants in the EBT group will receive focused, intensive instruction on using these skills to rewire unwanted brain circuits, with the aim of achieving lasting improvements in emotional health and quality of life. The study will assess whether EBT is an effective tool when added to standard of care (SOC), which includes medications for addiction treatment (MAT).
Researchers will compare changes in stress, anxiety, and cravings after 8 weeks of EBT plus SOC versus SOC alone.
Participants:
Full description
Background Information and Rationale Addiction is a neuropsychological disorder defined by a persistent and intense urge to use a drug or engage in a behavior that produces a natural reward, despite significant harm and negative consequences. Repetitive substance use alters brain function, perpetuating craving and weakening self-control, while not completely negating it. Addiction is now recognized as a complex brain disorder influenced by both neurobiological and psychosocial factors. Effective treatment typically combines pharmacological approaches with behavioral interventions, such as cognitive behavioral therapy (CBT), psychotherapy, behavior modification strategies, twelve-step programs, and structured residential care.
Emotional Brain Training (EBT) is a method of self-directed neuroplasticity targeting the neural root causes of addiction, rather than substituting one addiction for another. EBT addresses three primary brain-based contributors to addiction:
The core therapeutic technique of EBT is a structured emotional resiliency process that rewires maladaptive circuits through:
EBT uniquely targets brain circuits that control physiology. The same set of skills is applied by clinicians, in peer-to-peer support, and through self-care with mobile app support, enhancing access and scalability. Delivery occurs through small group telephonic sessions using a confidential platform that fosters learning, community, and coaching.
Group sessions are facilitated by licensed health professionals or certified coaches trained in personal and clinical EBT use. Emotional resiliency processes can be completed rapidly, ranging from two to three minutes for self-regulation to approximately twenty minutes for clinician-facilitated trauma rewiring. Practice is further reinforced through brief peer-to-peer sessions and mobile app exercises.
EBT effectiveness has been evaluated in 14 small studies, demonstrating improvements in psychological measures (such as depression, perceived stress, and self-efficacy), behavioral outcomes (including reduced addictive behaviors and increased exercise), and physiological markers (such as blood pressure and BMI).
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Inclusion criteria
Age 18 years old or older Patient can speak and read English Patient who receives regular MAT care at SAC Health Patients who have regular and reliable cellular and/or reliable internet connection Patients who are willing to spend average of 25 minutes per day and attend weekly group meetings Patients willing to actively participate in group sessions Opioid use disorder, at least in early remission Alcohol use disorder, at least in early remission Methamphetamine use disorder, at least in early remission Cocaine use disorder, at least in early remission Anxiolytic use disorder, at least in early remission Cannabis use disorder Tobacco use disorder
Exclusion criteria
Age <18 years old Patient does not speak or read English Patients who do not seek regular MAT care at SAC Health Patients with inconsistent or no access to cellular or internet connection Any disorder that is uncontrolled Any substance use disorder not in at least early remission Any patient with complications related to use disorder Patients enrolled in the Coachella Valley Rescue Mission patients a part of SAC Health Anyone who, in the opinion of the investigators, would be unable to participate in an 8-week trial
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54 participants in 2 patient groups
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Central trial contact
Brenda Boyle, DNP; Lori D Karan, MD
Data sourced from clinicaltrials.gov
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