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Assessing Top Down and Bottom Up Attention Mechanisms in Smokers Using Nicotine Nasal Spray

This study has been completed.
Sponsor:
Information provided by:
National Institutes of Health Clinical Center (CC)
ClinicalTrials.gov Identifier:
NCT01136642
First received: June 2, 2010
Last updated: May 3, 2013
Last verified: November 2012
History of Changes
  Purpose

Background:

  • Smoking is the leading cause of preventable death in the United States, and researchers are interested in gaining a better understanding of the perceived beneficial effects of nicotine to help improve treatment strategies for nicotine dependence. Understanding the conditions under which nicotine improves attention and cognitive processing may provide more useful information for this research.
  • The ability to pay attention and filter relevant from irrelevant stimuli is central to all aspects of information-processing. Top-down and bottom-up attentional processes illustrate how the brain combines stimuli and goal-directed behaviors. Bottom-up processing is an unconscious response to sensory input; for instance, when the eyes automatically focus on a prominent image in a picture. Top-down processing is a conscious response to drive attention toward specific stimuli; for instance, when a person is asked to focus on a less immediately noticeable image in a picture. Researchers are interested in determining whether nicotine improves cognitive performance by acting on top-down or bottom-up attentional mechanisms.

Objectives:

- To investigate the effect of nicotine on the top-down and bottom-up mechanisms of attention in cigarette smokers.

Eligibility:

- Current smokers (at least 10 cigarettes per day for at least 1 year) between 18 and 55 years of age.

Design:

  • This study will involve one training session and four experimental sessions.
  • During the training session, participants will receive a sample dose of the nicotine nasal spray used in the study to determine if they can tolerate the effects.
  • For each experimental session, participants will receive one dose of nicotine nasal spray (1 mg, 2 mg, or 3 mg) or placebo spray, followed by blood pressure and heart rate monitoring, performance of an attentional test, and questionnaires to rate participants' perception of nicotine effectiveness. Participants may receive different doses at different sessions, and will not be told which dose they will receive at any given point.

Condition Intervention Phase
Drug Addiction
Nicotine Dependence
 Drug: Nicotrol
 Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Pharmacokinetics/Dynamics Study
Intervention Model: Single Group Assignment
Masking: Double-Blind
Official Title: Assessing Top Down and Bottom Up Attention Mechanisms in Smokers Using Nicotine Nasal Spray

Resource links provided by NLM:

MedlinePlus related topics: Smoking
U.S. FDA Resources

Further study details as provided by National Institutes of Health Clinical Center (CC):

Primary Outcome Measures:
  • Performance (accuracy response time) on a test of selective attention.

Secondary Outcome Measures:
  • Vital signs, ratings of mood and drug effect.

Estimated Enrollment: 50
Study Start Date: January 2010
Study Completion Date: November 2012
Intervention Details:
    Drug: Nicotrol
    N/A
Detailed Description:

Objective:

The objective is to investigate the dose-response effect of nicotine on the top-down and bottom-up mechanisms of attention in cigarette smokers.

Study population:

Male and nonpregnant-female smokers 18 to 55 years of age.

Design:

This study is a double-blind, placebo controlled trial of nicotine or placebo nasal sprays. Participants have five visits: a training session and four experimental sessions. Each participant receives a test dose of the nasal spray immediately following the training session to ascertain tolerability and become familiarized with the effect of the spray. One dose (0, 1.0, 2.0 or 3.0 mg) of nicotine nasal spray is administered at the beginning of each experimental session followed by the test battery.

Outcome Measures:

Outcome measures are vital signs, ratings of mood and drug effect, and performance (accuracy, response time) on a test of selective attention.

  Eligibility

Ages Eligible for Study:   18 Years to 55 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

  • INCLUSION CRITERIA:

    1. 18-55 year old male and female cigarette smokers

    2. smoke a minimum of 10 cigarettes per day for at least 1 year

      --Drug Use Survey

    3. estimated IQ score greater than or equal to 85

      --Weschsler Abbreviated Scale of Intelligence (WASI; raw vocabulary cutoff 49)

    4. urine cotinine concentration greater than or equal 100 ng/ml

      • NicAlert(Registered Trademark) reading greater than or equal to 3

EXCLUSION CRITERIA:

  1. definite plan to quit smoking in next 30 days
  2. consumption of more than 15 alcoholic drinks per week during the past month

  3. use of any illicit drugs more than twice per week during the past month

    --Drug Use Survey (items 2-4)

  4. pregnant or nursing

    --Urine pregnancy test

  5. HIV positive

    --Oral HIV test

  6. untreated cardiovascular or pulmonary disease
  7. use of nicotine replacement products, bupropion or varenicline, in the past 3 months if specifically used to stop smoking

  8. Past history of schizophrenia or bipolar disorder.

    Current Major Depression Disorder, Diagnosis or treatment for Major Depressive Disorder in past 12 months. (H& P)

    Evidence of current ADHD by current diagnosis or medication or score on Adult Symptom Rating Scale; (> 16 on pt A or B must be evaluated by a counselor)

    • SCL-90 > 65 (must be evaluated by a counselor)
    • Beck Depression Inventory-II score greater than or equal to 14 (must be evaluated by a counselor)

  9. vital signs (must be outside these parameters on more than two occasions separated by at least one day):

    • systolic blood pressure: minimum 95, maximum 160 mm Hg
    • diastolic blood pressure: minimum 40, maximum 95 mm Hg
    • pulse: minimum 50, maximum 105 bpm
    • respirations: minimum 8, maximum 24 breaths per minute
  10. nasal passages: no pathology that would preclude administration of nasal spray
  11. under the influence of a drug or alcohol at experimental sessions
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01136642

Locations
United States, Maryland
National Institute on Drug Abuse, Biomedical Research Center (BRC)
Baltimore, Maryland, United States, 21224
Sponsors and Collaborators
National Institute on Drug Abuse (NIDA)
Investigators
Principal Investigator: Marilyn Huestis, Ph.D. National Institute on Drug Abuse (NIDA)
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT01136642     History of Changes
Other Study ID Numbers: 999910459, 10-DA-N459
Study First Received: June 2, 2010
Last Updated: May 3, 2013
Health Authority: United States: Federal Government

Keywords provided by National Institutes of Health Clinical Center (CC):
Nicotine
Nicotine Nasal Spray
Attention
Smoking

Additional relevant MeSH terms:
Tobacco Use Disorder
Substance-Related Disorders
Behavior, Addictive
Mental Disorders
Compulsive Behavior
Impulsive Behavior
Nicotine
Nicotine polacrilex
Ganglionic Stimulants
Autonomic Agents
Peripheral Nervous System Agents
 Physiological Effects of Drugs
Pharmacologic Actions
Nicotinic Agonists
Cholinergic Agonists
Cholinergic Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Central Nervous System Stimulants
Central Nervous System Agents
Therapeutic Uses

ClinicalTrials.gov processed this record on May 23, 2013