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N/A N=188 Randomized Double-blind Health Services Research

Reduced Nicotine Cigarettes in Smokers With Mood and Anxiety Disorders

Tobacco Dependence

Enrolled (actual)
188
Serious AEs
9.0%
Results posted
Feb 2019
Primary outcome: Primary: Plasma Cotinine Concentration — 82.8; 259.0 ng/mL — p=<0.0001

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Reduced Nicotine Content Cigarettes (Drug); Usual Nicotine Content Cigarettes (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Milton S. Hershey Medical Center
Primary completion
Jan 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Plasma Cotinine Concentration
82.8; 259.0 <0.0001 sig
SECONDARY
Quick Inventory of Depressive Symptomatology
5.5; 5.3 0.16
SECONDARY
Perceived Stress Scale
15.0; 15.1 0.67
SECONDARY
Minnesota Nicotine Withdrawal Scale
8.1; 9.0 0.65

Summary

The overall aim of this project is to evaluate the effect of progressive nicotine reduction in cigarettes on smoking behavior, toxin exposure and psychiatric symptoms in smokers with comorbid mood and/or anxiety disorders. Smokers with mood and/or anxiety disorder will smoke research cigarettes that will contain either a) nicotine content similar to their preferred usual brand of cigarettes, or b) nicotine content per cigarette that is progressively reduced from approximately 11.6 mg to 0.2 mg per cigarette over 18 weeks. It is our hypothesis that nicotine intake will decline as a function of cigarette nicotine content in the Reduced Nicotine Content group without significant increases in tobacco smoke exposure, severity of nicotine withdrawal symptoms, mood and anxiety symptomatology or protocol non-adherence over time in the Reduced Nicotine Content group as compared with the control group.

Eligibility Criteria

Inclusion Criteria

  • Smoke >4 cigarettes/day for at least a year
  • No quit attempt in prior month
  • Not planning to quit smoking within next 6 months
  • Plan to live in local area for next 8 months
  • Meet diagnostic criteria for a current or lifetime Anxiety Disorder or Mood Disorder as determined by the Mini-international Neuropsychiatric Interview
  • Read and write in English
  • Women not pregnant or nursing and taking steps to avoid pregnancy
  • Able to understand and consent to study procedures

Exclusion Criteria

  • Unstable or significant medical condition such as Chronic Obstructive Pulmonary Disease or kidney failure
  • Use of non-cigarette nicotine delivery product in the past week or smoking cessation medicine in prior month
  • Currently reducing or planning to reduce cigarette consumption in next month
  • Uncontrolled serious psychotic illness or substance abuse or inpatient treatment for these in the past 6 months
  • Current suicide risk on clinical assessment
  • Aged 65
  • History of difficulty providing blood samples (fainting, poor venous access)
  • Unwilling to remain on one flavor of cigarette (regular or menthol) for the duration of the trial
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01928758). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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