Effect of Behavioral Training on Physiological Responses to Smoking Cues, Affect and Cortisol

Completed · Phase 4

Conditions studied: Smokers

In brief

This study is ancillary. Participants will be recruited as part of a separate clinical trial on effects of two intensive behavioral training programs that evaluates feasibility and efficacy of a behavioral treatment that includes mindfulness techniques (MT) in comparison to traditional behavioral therapy (CBT) for smoking cessation. The investigators propose to compare the effect of MT to that of traditional CBT on a physiological marker of stress, salivary cortisol concentration, and physiological responses to smoking cues in tobacco smokers. The investigators will use electrophysiological reactivity to smoking cues in the form of audio recordings of personalized scripts describing the scenarios associated with the strongest urges to smoke that will provide a physiological validation to a behavioral intervention. The investigators will also explore correlations between these biological markers and self report of stress, craving and negative affect to supplement self report and behavioral outcome measures with biological and physiological markers to represent improvement attributed to the intervention.

Key facts

Study ID

NCT01362101

Run by

A. Eden Evins

People needed

56

Starts

2010-07-01

Expected to finish

2012-01-01

Last updated by the study team

2013-07-11

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Inclusion Criteria for the entire trial:
• Women and men aged 18-65, inclusive, who are competent, wish to participate and willing to provide informed consent.
• Self report smoking >=15 cigarettes/day.
• Expired air CO > 9ppm at the time of enrollment.
• Must be willing to participate in a meditation training group.
• Inclusion criteria for the physiological assessment:
• Abstinent for at least 12 hrs prior to the assessment.
• CO<15ppm
• Have negative urine toxicology for illicit drugs or alcohol.

You may not qualify if…

• DSM-IV diagnosis of dementia, neurodegenerative disease, or other organic mental disorder, lifetime history of psychotic disorder, bipolar disorder, severe PTSD, Dissociative Identity Disorder, OCD, anorexia nervosa, mental retardation, or autism.
• History of moderate or severe major depressive episode or generalized anxiety disorder within the last 6 months.
• Use of prescribed psychotropic medication other than SSRI/NDRI/SNRI/ buprenorphine in past 6mo, or change in such psychiatric medication dose in past six months.
• History of active substance use disorder other than nicotine or caffeine in the last 6 months.
• Positive urine toxicology for illicit drugs, alcohol, opiates or benzodiazepines.
• Serious unstable medical illness including, cardiovascular, hepatic, renal, respiratory, endocrine, neurological, or hematological disease such that hospitalization for treatment of that illness is likely within the next 4 months. History of life-threatening arrhythmia, CHF, syncope, or myocardial infarction within the last year. Abnormal cardiovascular event, or uncontrolled hypertension within last 2 months.
• History of cerebro-vascular events (i.e., stroke, TIA), multiple head injuries with neurological sequelae, a single severe head injury with lasting neurological sequelae, history of seizure disorder or current CNS tumor.
• Use of investigational medication in the past 30 days.
• Inability to speak, read, or understand English.

Where it is running

• Center For Addiction Medicine-Massachusetts General Hospital — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

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