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Treatment of Smoking Lapses and Relapses

Treatment of Smoking Lapses and Relapses

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01807871
Enrollment
701
Registered
2013-03-08
Start date
2013-03-31
Completion date
2016-02-29
Last updated
2017-10-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking Cessation

Keywords

nicotine dependence, smoking cessation, lapse, relapse, tobacco, nicotine patch, nicotine replacement therapy, NRT

Brief summary

Many smokers who try to stop smoking with nicotine medications (NM) such as gum, lozenge and patch, go back to smoking (i.e., a slip or lapse). Currently, labeling on many NM products tells smokers who lapse while using NM to stop NM. However, some studies suggest it is safe to continue NM upon a lapse and that doing so dramatically increases success at quitting. The investigators will test this by doing a randomized trial in which all treatment and measures are done from home with paper, phone or computer surveys. The investigators will recruit smokers who want to quit, provide them with 10 weeks of nicotine patch treatment and 5 weeks of counseling. One group will be asked to stop use of the patch if they lapse and the other group will be asked to continue use of the patch if they lapse. The investigators will compare the groups on their success at quitting and side-effects.

Detailed description

Objectives: To test our hypothesis that among the subset of the 770 enrolled participants who quit smoking and then lapsed while using the nicotine patch, those randomized to continue the patch post-lapse will be more likely to be 7-day point prevalent abstinent at 4-month follow-up than those randomized to discontinue the patch post-lapse. To test whether the amount of patch use post-lapse, craving, withdrawal, cigs/day, motivation to quit, confidence in quitting, nicotine reinforcement from cigarettes, and self-efficacy mediate any effect of post-lapse patch use on abstinence. To test whether the incidence of adverse events (AEs) during post-lapse patch use is minimal. Purpose: Over the counter (OTC) NRT is, by far, the most common treatment for smoking cessation in the United States (Cokkinides, Ward, Jemel, & Thun, 2005). Over 80% of those using OTC NRT will lapse (Stead, Perera, Bullen, Mant, & Lancaster, 2008). One possible reason for this high rate of relapse is that NRT package labeling states do not use if you continue to smoke, and the majority of smokers believe this means it is best to stop using NRT upon a lapse; e.g., the only survey on real-world use of NRT during a lapse episode found that 77% of smokers discontinued NRT after a lapse (Pierce & Gilpin, 2002). The investigators and others (Bader, McDonald, & Selby, 2009) believe continuing NRT during a lapse episode will a) relieve craving and withdrawal (West & Shiffman, 2001), b) block the reinforcing effects of smoking (Perkins, Fonte, Meeker, White, & Wilson, 2001; Rose & Behm, 2004), c) help smokers smoke less (Hughes & Carpenter, 2005), and d) increase self-efficacy, all of which should help smokers re-establish abstinence. Study design: The investigators are proposing a parallel groups randomized controlled trial (RCT) in which all treatment and monitoring occur via phone, and medication via mail. The investigators will recruit about 770 smokers to receive phone counseling before and after the quit date and nicotine patches for 10 weeks after the quit date. At study entry, smokers will be randomized to a Continue NRT or a Discontinue NRT condition. The Continue NRT participants will be advised that, if they lapse, they should continue NRT. Smokers randomized to the Discontinue NRT condition will be advised that, if they lapse, they should discontinue NRT use. The messages will also include rationales. Messages will be delivered several times via written material, Interactive Voice Response (IVR) messages and during phone counseling. Participants will record cigs/day nightly via a phone-based IVR system for 10 weeks. If the IVR detects a lapse during the first 10 weeks of the study, it will encourage the participant to re-establish abstinence as soon as possible and repeat the condition-appropriate message about post-lapse NRT use. After the 10-week treatment period, the investigators will use monthly questionnaires (online or paper) to assess recent smoking, cigs/day, NRT use, and other stop-smoking medications. Subject selection: Men and women, minorities and children over 18 will be included. Pregnant and breastfeeding women, women who plan to become pregnant and those at risk for AEs from NRT will be excluded. Our goal is to recruit a sample of the same gender, ethnicity/race prevalence as that of US smokers interested in quitting; i.e. 52% men, 78% White/Non-Hispanic, 11% Black, 8% Hispanic and 3% other ethnicities/races (Hughes & Callas, 2010). The investigators do not have data on which to estimate the percent who will be children between ages 18-21 but most studies suggest very few young smokers are interested in formal treatment (Sussman, 2002). Number of subjects: The investigators have chosen an initial inclusion of 770 smokers to obtain a sample size of 490 smokers who lapse on NRT.

Interventions

DRUGnicotine patch, experimental use

nicotine patch-transdermal, continue during lapses Nicotine patches are used according to normal package label, except if the participant lapses and smokes, they will continue to use the patch.

DRUGnicotine patch, labeled use

nicotine patch-transdermal, discontinue during lapses Participants will use the nicotine patch while abstinent, but will remove the patch if there is a lapse and smoking resumes. This is the use indicated on current FDA approved labeling.

Sponsors

National Cancer Institute (NCI)
CollaboratorNIH
University of Vermont
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* at least 18 years old * daily smoker of 10 or more cigarettes per day for at least 1 year * state they plan to probably or definitely quit smoking in the next month * have a home or cell phone * willing to use nicotine patch * good command of written and spoken English * weigh at least 100 pounds * US citizen or permanent resident alien

Exclusion criteria

* use of non-cigarette tobacco in the last month * use of a smoking cessation medication or smoking cessation counseling in the last month * medical contraindication to use of patch * other person in household already in our study * previously a participant in the study * currently pregnant or breast feeding * plan to become pregnant in the next 6 months * regularly works the overnight shift * use of electronic cigarettes in the last month

Design outcomes

Primary

MeasureTime frameDescription
Point-prevalent Abstinence at 4 Months4 months after the quit dateTo test our hypothesis that among the subset of the 701 enrolled participants who quit smoking and then lapsed while using the nicotine patch, those randomized to continue the patch post-lapse will be more likely to be 7-day point-prevalent abstinent at 4 month follow-up than those randomized to discontinue the patch post-lapse. 7-day point prevalent abstinence was assessed by response to the question In the last 7 days, on how many days did you smoke on the 4 month follow-up survey. Respondents who replied 0 were classified as Yes for 7-day point-prevalent abstinence; all other responses (including missing) were classified as No.

Secondary

MeasureTime frameDescription
Mediators of Effect of Post-lapse Nicotine Replacement Therapy Use on Abstinence4 months after the quit dateTo test whether the amount of use of nicotine patch post-lapse, craving, withdrawal, cigs/day, motivation to quit, confidence in quitting, nicotine reinforcement from cigarettes, and self-efficacy mediate any effect of post-lapse patch use on abstinence.
Adverse Drug EffectsUp to 12 weeksTo test whether the incidence of adverse drug effects during the post-lapse use of nicotine patch is minimal.

Countries

United States

Participant flow

Recruitment details

Recruitment between April 2013 and July 2015

Participants by arm

ArmCount
Nicotine Patch, Experimental Use
Participants will continue to use nicotine patch after they lapse and resume smoking as long as smoking is less than 75% of pre study levels. nicotine patch, experimental use: nicotine patch-transdermal, continue during lapses Nicotine patches are used according to normal package label, except if the participant lapses and smokes, they will continue to use the patch.
356
Nicotine Patch, Labeled Use
Participants will discontinue using the nicotine patch when they resume smoking. This is the current FDA approved use of the nicotine patches. nicotine patch, labeled use: nicotine patch-transdermal, discontinue during lapses Participants will use the nicotine patch while abstinent, but will remove the patch if there is a lapse and smoking resumes. This is the use indicated on current FDA approved labeling.
345
Total701

Baseline characteristics

CharacteristicNicotine Patch, Experimental UseNicotine Patch, Labeled UseTotal
Age, Continuous44 years
STANDARD_DEVIATION 11
45 years
STANDARD_DEVIATION 12
45 years
STANDARD_DEVIATION 12
Race/Ethnicity, Customized
Black Non-Hispanic
128 Participants123 Participants251 Participants
Race/Ethnicity, Customized
Hispanic
45 Participants32 Participants77 Participants
Race/Ethnicity, Customized
Other
12 Participants11 Participants23 Participants
Race/Ethnicity, Customized
White Non-Hispanic
170 Participants179 Participants349 Participants
Region of Enrollment
United States
356 participants345 participants701 participants
Sex: Female, Male
Female
190 Participants207 Participants397 Participants
Sex: Female, Male
Male
166 Participants138 Participants304 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
1 / 3561 / 345
other
Total, other adverse events
196 / 356187 / 345
serious
Total, serious adverse events
4 / 3564 / 345

Outcome results

Primary

Point-prevalent Abstinence at 4 Months

To test our hypothesis that among the subset of the 701 enrolled participants who quit smoking and then lapsed while using the nicotine patch, those randomized to continue the patch post-lapse will be more likely to be 7-day point-prevalent abstinent at 4 month follow-up than those randomized to discontinue the patch post-lapse. 7-day point prevalent abstinence was assessed by response to the question In the last 7 days, on how many days did you smoke on the 4 month follow-up survey. Respondents who replied 0 were classified as Yes for 7-day point-prevalent abstinence; all other responses (including missing) were classified as No.

Time frame: 4 months after the quit date

Population: Participants who lapsed while using the nicotine patch

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Nicotine Patch, Experimental UsePoint-prevalent Abstinence at 4 Months90 Participants
Nicotine Patch, Labeled UsePoint-prevalent Abstinence at 4 Months59 Participants
p-value: 0.48Chi-squared
Secondary

Adverse Drug Effects

To test whether the incidence of adverse drug effects during the post-lapse use of nicotine patch is minimal.

Time frame: Up to 12 weeks

Population: All randomized participants

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Nicotine Patch, Experimental UseAdverse Drug Effects37 Participants
Nicotine Patch, Labeled UseAdverse Drug Effects27 Participants
Comparison: Comparison of number of participants who reported removing the nicotine patch due to a side effectp-value: 0.24Chi-squared
Secondary

Mediators of Effect of Post-lapse Nicotine Replacement Therapy Use on Abstinence

To test whether the amount of use of nicotine patch post-lapse, craving, withdrawal, cigs/day, motivation to quit, confidence in quitting, nicotine reinforcement from cigarettes, and self-efficacy mediate any effect of post-lapse patch use on abstinence.

Time frame: 4 months after the quit date

Population: Because the results for the primary outcome were negative, this outcome was not analyzed (i.e., there was no effect to mediate).

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026