Effects of Nicotine on Elements of Attentions in Smokers and Nonsmokers

June 30, 2017 updated by: National Institute on Drug Abuse (NIDA)

Background:

- Many cigarette smokers claim that smoking helps them stay alert and improves their concentration, and have reported problems in attention and concentration after quitting smoking. Some research has indicated that nicotine can enhance certain aspects of attention and memory in humans. However, more research is needed to determine how nicotine affects different elements of the brain's ability to pay attention. Knowing which aspects of attention are affected by nicotine may help produce new medications and therapies to help people successfully stop smoking.

Objectives:

  • To investigate the dose-related effects of nicotine on the ability to pay attention in smokers and nonsmokers.
  • To compare the effects of nicotine in smokers and nonsmokers.

Eligibility:

- Individuals between 18 and 50 years of age who are either current smokers (at least 15 cigarettes per day on average for at least 2 years) or healthy, nonsmoking volunteers.

Design:

  • The study will consist of one training session and three testing sessions. Each session will last about 2 hours.
  • The training session will introduce participants to the study tests and evaluate their tolerance of the two levels of nicotine nasal spray used in the study. Smokers will receive the higher dose of nicotine to introduce them to the effects of the spray. Nonsmokers will be given first the lower dose of the spray, followed by higher dose at least 30 minutes later. Nonsmoking participants who cannot tolerate the higher dose will not continue in the study.
  • At the start of each testing session, smokers will have one cigarette to standardize the time of the most recent exposure to nicotine.
  • During the testing sessions, participants will receive a placebo spray, a lower dose of nicotine, or a higher dose of nicotine, and then will be asked to perform tests that evaluate mood, attention, and performance.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Objective: The primary objective of this study is to investigate the dose-related effects of nicotine on various elements of attention in smokers and nonsmokers. Because no published study, to our knowledge, has reported the effects of nicotine on the ANT and ABT, we will include the CPT, a task shown to be sensitive to nicotine, as a positive control. A secondary aim is to compare the subjective and physiological effects of nicotine between smokers and nonsmokers.

Study Population: 50 smokers for a total of 30 completers (15 women, 15 men) and up to 50 nonsmokers for a total of 30 completers (15 women, 15 men).

Design: Placebo-controlled, between-groups comparison of smokers and nonsmokers. Participants will attend three experiemental sessions; a single dose of nicotine nasal spray (0, 0.5, or 1.5 mg) will be administered at each session.

Outcome Measures: Primary outcome measures will be accuracy and/or response time on the three attention tests, ANT, CPT, and ABT. Secondary outcome measures include responses to the PANAS, VAS items, and vital signs (heart rate and blood pressure). Participant demographics and smoking history will be reported using descriptive statistics.

Study Type

Interventional

Enrollment (Anticipated)

100

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Maryland
      • Baltimore, Maryland, United States, 21224
        • National Institute on Drug Abuse, Biomedical Research Center (BRC)

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 50 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

  • INCLUSION CRITERIA: Smokers

    1. be men and women 18-50 years old
    2. report smoking at least 15 cigarettes per day on average for at least 2 years
    3. have a urine cotinine level greater than or equl to 200 ng/ml
    4. have an estimated IQ score greater than or equal to 85
    5. be medically and psychologically healthy as determined by screening criteria

      EXCLUSION CRITERIA: Smokers

    1. be interested in reducing or quitting tobacco use
    2. have been treated for nicotine dependence in the past 3 months 3) report a history of drug or alcohol dependence

    4) report consumption of more than 15 alcoholic drinks per week during the past month

    5) report use of marijuana more than once per week during the past month

    6) report use of any illicit drug, other than marijuana, during the past 6 months

    7) be currently using any medication that would interfere with the protocol

    8) be under the influence of a drug or alcohol at experimental sessions

    9) be pregnant or nursing

    10) be HIV positive.

INCLUSION CRITERIA: Nonsmokers

  1. be men and women 18-50 years old
  2. report smoking less than 10 cigarettes in their life
  3. have a urine cotinine level less than 30 ng/ml
  4. have an estimated IQ score greater than or equal to 85
  5. be medically and psychologically healthy as determined by screening criteria

EXCLUSION CRITERIA: Nonsmokers

  1. report use of any tobacco products in the past 3 years
  2. report a history of drug or alcohol dependence
  3. report consumption of more than 15 alcoholic drinks per week during the past month
  4. report use of marijuana more than once per week during the past month
  5. report use of any illicit drug, other than marijuana, during the past 6 months
  6. be currently using any medication that would interfere with the protocol
  7. be under the influence of a drug or alcohol at experimental sessions
  8. be pregnant or nursing
  9. be HIV positive.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Pharmacodynamics, changes in cognitive function

Secondary Outcome Measures

Outcome Measure
Changes in subjective mood, changes in cardiovascular measures

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

February 14, 2006

Primary Completion (Actual)

November 3, 2009

Study Completion (Actual)

November 3, 2009

Study Registration Dates

First Submitted

December 16, 2009

First Submitted That Met QC Criteria

December 16, 2009

First Posted (Estimate)

December 17, 2009

Study Record Updates

Last Update Posted (Actual)

July 2, 2017

Last Update Submitted That Met QC Criteria

June 30, 2017

Last Verified

September 22, 2010

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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