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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02416986
Other study ID # Pro00056221
Secondary ID R01DA038442-01
Status Completed
Phase N/A
First received April 8, 2015
Last updated January 30, 2017
Start date October 2014
Est. completion date December 2015

Study information

Verified date August 2016
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this study is to evaluate the effects of exposure to standard smoking environments on ability to resist smoking as measured with a Delay to Smoking Task. The results of this study will inform whether the Delay to Smoking Task is a sensitive measure for evaluating environment-provoked craving and smoking behavior.


Description:

Adult smokers (n=25) will complete 4 visits and a 6 month follow-up phone call. Participants will complete a Delay to Smoking Task following 6 hours smoking abstinence. The task involves viewing pictures of smoking and non-smoking locations and participants will have the choice to smoke a cigarette at any time during the session. A monetary reinforcer will be provided for each 6-minute period that a participant resists smoking. Once participants stop the task they can choose to smoke as much or a little as they want for the next 30 minutes. Participants will be provided with a smoking tab. Each cigarette they light will cost them from their tab. Measurements of tobacco craving, emotion ratings, and nicotine withdrawal will be assessed.


Recruitment information / eligibility

Status Completed
Enrollment 41
Est. completion date December 2015
Est. primary completion date July 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- generally healthy

- between the ages of 18 and 55

- smoking an average of 5 cigarettes per day for at least one year

- breath CO level > 8 ppm (if = 8 ppm, then NicAlert Strip = 6)

- no interest in quitting smoking for the duration of time required for the experiment

Exclusion Criteria:

- inability to attend all required experimental sessions

- use of psychoactive medications

- use of smokeless tobacco

- current alcohol or drug abuse

- use of illegal drugs as measured by urine drug screen (excluding marijuana)

- current use of nicotine replacement therapy or other smoking cessation treatment

- Blood Alcohol Level (BAL) > 0.00

- use of other tobacco products or e-cigarettes more than 9 days in the past 30 days

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
6 hour smoking abstinence

Delay to Smoking Task (smoking cues)
Participants will be presented with an unlit cigarette of their brand and an opportunity to initiate ad lib smoking at any time during the 60-minute task. During this period, participants will be allowed to read books or magazines, but will hear a tone alerting them to view cues (standard smoking environments) for the final minute of each 6-minute period. A monetary reinforcer will be provided for each 6-minute period that a participant resists smoking. Once participants stop the task they can choose to smoke as much or a little as they want for the next 30 minutes. Participants will be provided with a smoking tab. Each cigarette they light will cost them from their tab.
Delay to Smoking Task (nonsmoking cues)
Participants will be presented with an unlit cigarette of their brand and an opportunity to initiate ad lib smoking at any time during the 60-minute task. During this period, participants will be allowed to read books or magazines, but will hear a tone alerting them to view cues (standard nonsmoking environments) for the final minute of each 6-minute period. A monetary reinforcer will be provided for each 6-minute period that a participant resists smoking. Once participants stop the task they can choose to smoke as much or a little as they want for the next 30 minutes. Participants will be provided with a smoking tab. Each cigarette they light will cost them from their tab.

Locations

Country Name City State
United States Duke University Medical Center Durham North Carolina

Sponsors (3)

Lead Sponsor Collaborator
Duke University National Institute on Drug Abuse (NIDA), National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in self-report craving measured by the cue-exposure rating scale at 0 minutes, +30 minutes, +60 minutes and following first cigarette
Primary Difference in number of subjects who initiate smoking during the smoking cue Delay to Smoking Task compared to the nonsmoking cue Delay to Smoking Task If participant initiates smoking a cigarette during the Delay to Smoking Task following start of Delay to Smoking Task, up to 60 minutes
Primary Number of minutes to first puff Number of minutes to first puff of cigarette will be recorded for participants that initiate smoking following start of Delay to Smoking Task, up to +60 minutes
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