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fMRI Study of a Dual Process Treatment Protocol With Substance Dependent Adults

fMRI Study of a Dual Process Treatment Protocol With Substance Dependent Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01320748
Enrollment
29
Registered
2011-03-22
Start date
2011-02-28
Completion date
2013-01-31
Last updated
2018-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Substance Abuse, Substance Dependence, Alcohol Abuse, Drug Use, Relapse

Keywords

Abstinence from alcohol, Substance Abuse and Mental Health Services, Social Support, Psychosocial Support Systems, Psychological support, Cognitive Support, Emotional Support, Mental Support, Psychosocial Support, Intervention Studies, Prevention & control, Preventive therapy, Treatment, Therapy, Magnetic Resonance Imaging, fMRI, Imaging, Magnetic Resonance Imaging, Functional, MRI Scans, MRI, Functional, Clinical Protocols, Protocols, Treatment, Drug Abuse Treatment Center, Substance Abuse Treatment Center

Brief summary

The purpose of this study is to determine whether drug-dependent adults who participate in a dual processing relapse prevention treatment protocol that allows for sensory-based exposure experiences over 10-weeks in outpatient treatment will show significant brain change related to diminished cue reactivity, and greater improvement in self-efficacy, anxiety, somatization, and treatment retention, as compared to the standard care patients in a relapse prevention program.

Detailed description

The substance abuse literature consistently shows that negative emotional states and subjective stress are highly predictive of relapse and significantly influence behavioral motivation. From a neurobiological perspective, stress associated with withdrawal and substance abuse experiences stimulates chemical and hormonal changes in the brain creating a protracted hyperaroused state. Further, cognitive control resources (i.e., cognitive coping skills/relapse prevention training) have been shown to exert minimal impact on behavioral decision-making in the presence of intense affective material. Thus, implicit cognitive processes play a significant role in drug use behavior, decreasing self regulation capacities and increasing risk of. Specifically, high levels of stress can compromise prefrontal cortex functioning, with the nucleus accumbens, orbitofrontal cortex and amygdala functional changes related to increased cue reactivity. Taken together, the current literature strongly suggests that verbally-based therapies may have limited utility as a singular form of treatment in early substance abuse recovery, as the brain may not be functionally ready for executive level processing. Instead, the multidisciplinary substance abuse literature suggests that psychosocial treatment methods need to include a range of learning approaches that allow for visual-sensory processing, in addition to traditional verbal-based processing. Integrated multi-modal interventions are needed to offer opportunities for activation of these different brain regions to facilitate cognitive-affective balance in behavioral decision-making.

Interventions

BEHAVIORALDual Processing

A 10-week, 20-session program, which meets two times per week for 2 hours each time. It is a psychosocial intervention that combines a visual processing (structured drawing activities to engage in sensory-based cue exposure) and a verbal processing component (structured cognitive-behavioral therapy). The treatment focuses on sensory-based emotional expression and cognitive reappraisal and containment strategies that facilitate emotional regulation around a patient's drug and alcohol use experiences.

The program's standard care outpatient program is a Relapse Prevention 10-week, 20-session, psychosocial intervention program, which meets two times per week for 2 hours each time. This RP program is based on Gorski's Relapse Prevention model and is a primarily didactic approach.

Sponsors

George Mason University
CollaboratorOTHER
Georgetown University
CollaboratorOTHER
Inova Health Care Services
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Study Inclusion Criteria: * Age \< 18 years old * Signed informed consent for this study * History of chemical dependency * Meets Inova CATS Relapse Prevention admission criteria * Must have at least 60 days of sobriety prior to admission with documentation of negative drug and alcohol screening * Documentation of HIV negative test result (completed in the past year) * Willing and able to attend an out-patient drug treatment group for two hours twice a week for 10 weeks * Willing to complete study-required evaluations (including assessments, questionnaires, drug/alcohol testing, week 8 qualitative interview) * A score \< 25 on the MoCA (Montreal Cognitive Assessment) Study

Exclusion criteria

* History of taking anti-craving medication in the past 90 days * Other medical illness or florid psychiatric symptoms that would render the participant inappropriate for study participation * History of receiving treatment for addictions other than substance use (i.e. food, gambling, sex) * Clinical determination of dementia or organic brain syndrome * History of major head injury * Incapable of consenting for themselves due to cognitive impairment * Enrollment in another study that might interfere with analysis of this study Additional Inclusion Criteria for fMRI sub-study: * Willing and able to participate in the fMRI arm of the study * If of childbearing capacity, must have negative screening urine pregnancy test and be willing to use birth control as specified in the consent document Additional

Design outcomes

Primary

MeasureTime frameDescription
fMRI blood-oxygenation-level-dependent (BOLD) signal change as a measure of emotional reactivity related to the visual presentation of drug-imagery.10 weeksIn a subset of approximately 26 subjects, fMRI technology will be employed to examine brain structure and function change (pre-treatment and post-treatment) in the amygdaloid region, orbitofrontal cortex, in the anterior cingluate cortex (structure implicated in drug cue attention); in medial prefrontal cortex and right dorsolateral prefrontal cortex (associated with effective behavioral decision-making in substance abusers).

Secondary

MeasureTime frameDescription
Quality of Life Inventory (QOLI) as a measure of the subject's quality of life.10 weeksQuestionnaire completed by subjects at baseline and at the end of the study. We will measure changes in Overall QOLI score and Weighted Satisfaction Profile score at the two time-points (pre-intervention and post-intervention).
Brief Symptoms Inventory (BSI), as a measure of subjective craving, anxiety, and somatization10 weeksQuestionnaire completed by subjects at baseline and at the end of the study. We will measure changes in Nonpatient T Score and Percentile in the 12 domains at the two time-points (pre-intervention and post-intervention).
Heart rate during MRI scanning as a measure of emotional reactivity related to the visual presentation of drug-imagery.10 weeksChanges in heart rate related to the visual presentation of drug-imagery during MRI scanning, to assess cue reactivity differences across the treatment and control groups at two time-points (pre-intervention and post-intervention).
Urine specimen toxicology analysis as a measure of treatment retention.Weekly for 10 weeksUrine specimen collection and analysis to track patient drug use on a weekly basis during the 10 weeks in treatment.
Blood Alcohol Level analysis as a measure of treatment retention.Weekly for 10 weeksBreathalizer test for alcohol to track patient alcohol use on a weekly basis during the 10 weeks in treatment.
Hamilton - Depression Inventory (HAM-D) as a measure of depression.10 weeksQuestionnaire completed by subjects at baseline and at the end of the study. We will measure changes in the total Hamilton depression scale score at the two time-points (pre-intervention and post-intervention).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026