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1.
J Clin Psychiatry ; 78(8): 1075-1082, 2017.
Article in English | MEDLINE | ID: mdl-28199070

ABSTRACT

OBJECTIVE: To evaluate exercise as a treatment for stimulant use disorders. METHODS: The STimulant Reduction Intervention using Dosed Exercise (STRIDE) study was a randomized clinical trial conducted in 9 residential addiction treatment programs across the United States from July 2010 to February 2013. Of 497 adults referred to the study, 302 met all eligibility criteria, including DSM-IV criteria for stimulant abuse and/or dependence, and were randomized to either a dosed exercise intervention (Exercise) or a health education intervention (Health Education) control, both augmenting treatment as usual and conducted thrice weekly for 12 weeks. The primary outcome of percent stimulant abstinent days during study weeks 4 to 12 was estimated using a novel algorithm adjustment incorporating self-reported Timeline Followback (TLFB) stimulant use and urine drug screen (UDS) data. RESULTS: Mean percent of abstinent days based on TLFB was 90.8% (SD = 16.4%) for Exercise and 91.6% (SD = 14.7%) for Health Education participants. Percent of abstinent days using the eliminate contradiction (ELCON) algorithm was 75.6% (SD = 27.4%) for Exercise and 77.3% (SD = 25.1%) for Health Education. The primary intent-to-treat analysis, using a mixed model controlling for site and the ELCON algorithm, produced no treatment effect (P = .60). In post hoc analyses controlling for treatment adherence and baseline stimulant use, Exercise participants had a 4.8% higher abstinence rate (78.7%) compared to Health Education participants (73.9%) (P = .03, number needed to treat = 7.2). CONCLUSIONS: The primary analysis indicated no significant difference between exercise and health education. Adjustment for intervention adherence showed modestly but significantly higher percent of abstinent days in the exercise group, suggesting that exercise may improve outcomes for stimulant users who have better adherence to an exercise dose. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT01141608.


Subject(s)
Central Nervous System Stimulants/pharmacology , Exercise Therapy , Exercise/physiology , Health Education/methods , Substance-Related Disorders , Adult , Diagnostic and Statistical Manual of Mental Disorders , Exercise Therapy/methods , Exercise Therapy/psychology , Female , Humans , Male , Middle Aged , Patient Compliance/psychology , Substance-Related Disorders/diagnosis , Substance-Related Disorders/etiology , Substance-Related Disorders/psychology , Substance-Related Disorders/therapy , Treatment Outcome
2.
J Addict Med ; 7(1): 8-16, 2013.
Article in English | MEDLINE | ID: mdl-23188041

ABSTRACT

OBJECTIVE: : Determining the brain substrates underlying the motivation to abuse addictive drugs is critical for understanding and treating addictive disorders. Laboratory neuroimaging studies have demonstrated differential activation of limbic and motivational circuitry (eg, amygdala, hippocampus, ventral striatum, insula, and orbitofrontal cortex) triggered by cocaine, heroin, nicotine, and alcohol cues. The literature on neural responses to marijuana cues is sparse. Thus, the goals of this study were to characterize the brain's response to marijuana cues, a major motivator underlying drug use and relapse, and determine whether these responses are linked to self-reported craving in a clinically relevant population of treatment-seeking marijuana-dependent subjects. METHODS: : Marijuana craving was assessed in 12 marijuana-dependent subjects using the Marijuana Craving Questionnaire-Short Form. Subsequently, blood oxygen level dependent functional magnetic resonance imaging data were acquired during exposure to alternating 20-second blocks of marijuana-related versus matched nondrug visual cues. RESULTS: : Brain activation during marijuana cue exposure was significantly greater in the bilateral amygdala and the hippocampus. Significant positive correlations between craving scores and brain activation were found in the ventral striatum and the medial and lateral orbitofrontal cortex (P < 0.0001). CONCLUSIONS: : This study presents direct evidence for a link between reward-relevant brain responses to marijuana cues and craving and extends the current literature on marijuana cue reactivity. Furthermore, the correlative relationship between craving and brain activity in reward-related regions was observed in a clinically relevant sample (treatment-seeking marijuana-dependent subjects). Results are consistent with prior findings in cocaine, heroin, nicotine, and alcohol cue studies, indicating that the brain substrates of cue-triggered drug motivation are shared across abused substances.


Subject(s)
Amygdala , Brain Mapping/methods , Cues , Hippocampus , Magnetic Resonance Imaging/methods , Marijuana Abuse , Photic Stimulation/methods , Adult , Amygdala/pathology , Amygdala/physiopathology , Behavior, Addictive/diagnosis , Behavior, Addictive/physiopathology , Diagnostic and Statistical Manual of Mental Disorders , Female , Hippocampus/pathology , Hippocampus/physiopathology , Humans , Male , Marijuana Abuse/diagnosis , Marijuana Abuse/physiopathology , Marijuana Abuse/psychology , Middle Aged , Patient Acceptance of Health Care , Predictive Value of Tests , Psychiatric Status Rating Scales , Psychological Techniques , Recurrence , Reward , Substance Abuse Detection/methods
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