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De-nicotinised Cigarettes Study (Denic)

Primary Purpose

Smoking Cessation, Tobacco Dependence

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
De-nicotinised cigarettes + standard treatment
Standard Treatment
Sponsored by
Queen Mary University of London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Smoking Cessation focused on measuring Smoking Cessation, Tobacco Dependence, De-nicotinised cigarettes

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 18 years or over
  • Seeking treatment to stop smoking

Exclusion Criteria:

  • Pregnant or breastfeeding
  • Acute psychiatric illness

Sites / Locations

  • Tobacco Dependence Research Unit

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

De-nicotinised cigarettes + standard treatment

Standard treatment

Arm Description

Outcomes

Primary Outcome Measures

Urges to smoke in first week of abstinence
Differences in urges to smoke in the first week of abstinence between participants who receive a behavioural replacement (DNCs) plus standard NHS SSS treatment, with those who receive standard NHS SSS treatment alone, will be measured by the Mood and Physical Symptoms Scale (MPSS; West & Hajek, 2004).

Secondary Outcome Measures

Change in ratings of tobacco withdrawal symptoms, measured by the MPSS
CO-validated continuous abstinence rates
CO-validated continuous abstinence rates will be measured 1-4 weeks following the target quit day in the standard treatment condition and 1-4 weeks following cessation of DNCs in the DNC condition.
Acceptability and user reactions to DNCs
Urges to smoke 24 hours after quitting, measured by the MPSS
Profile of adverse effects up to 12 weeks post quitting
Reactions to smoking cues
The differences in reactions to smoking cues between the 2 groups will be measured with smoking-related images and by the Cue Exposure Subscale of the Wisconsin Inventory for Smoking Dependence (WISDM-68; Piper, et al., 2004).

Full Information

First Posted
November 29, 2010
Last Updated
July 16, 2012
Sponsor
Queen Mary University of London
Collaborators
Pfizer
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1. Study Identification

Unique Protocol Identification Number
NCT01250301
Brief Title
De-nicotinised Cigarettes Study
Acronym
Denic
Official Title
Complementing Current NHS Stop Smoking Service Treatments for Smokers With Behavioural Replacement: The Role of De-nicotinised Cigarettes
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
April 2012 (Actual)
Study Completion Date
July 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Queen Mary University of London
Collaborators
Pfizer

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this study is to determine if using a behavioural replacement for smoking (de-nicotinised cigarettes; DNCs), in addition to standard treatment during the first two weeks after the target quit date, can reduce urges to smoke over the first 4-weeks of abstinence. Two hundred smokers who want to quit will be recruited from the community. They would all receive standard smoking cessation treatment from the NHS Stop Smoking Service (NHS SSS), which uses a combination of stop smoking medication (e.g. nicotine replacement therapy, Champix) and motivational support. On their target quit date, participants would be randomised to receive behavioural replacement ( i.e. use of de-nicotinised cigarettes) plus standard treatment for the first two weeks of their quit attempt, or to continue with standard treatment alone. De-nicotinised cigarettes are similar to standard cigarettes except that they do not deliver nicotine to the smoker. Participants will rate their urges to smoke at each week. Standard NHS SSS measures will also be taken in addition to user acceptability ratings and reactions to smoking cues. The hypothesis is that complementing current NHS SSS treatments with de-nicotinised cigarettes, to address the non-nicotine factors associated with smoking and to help extinguish smoking behaviour, would result in lower urges to smoke than standard treatment alone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Smoking Cessation, Tobacco Dependence
Keywords
Smoking Cessation, Tobacco Dependence, De-nicotinised cigarettes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
De-nicotinised cigarettes + standard treatment
Arm Type
Experimental
Arm Title
Standard treatment
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
De-nicotinised cigarettes + standard treatment
Other Intervention Name(s)
NHS Stop Smoking Service, De-nicotinised cigarettes
Intervention Description
Participants will receive de-nicotinised cigarettes to use as required for 2 weeks after their quit day. These cigarettes are intended to provide a replacement for the behavioural and sensory aspects of smoking without supplying nicotine. Participants will also receive standard NHS Stop Smoking Service treatment. This is a combination of weekly behavioural support and medication (e.g. nicotine replacement therapy/varenicline).
Intervention Type
Other
Intervention Name(s)
Standard Treatment
Intervention Description
Participants will receive standard treatment from the NHS Stop Smoking Service.
Primary Outcome Measure Information:
Title
Urges to smoke in first week of abstinence
Description
Differences in urges to smoke in the first week of abstinence between participants who receive a behavioural replacement (DNCs) plus standard NHS SSS treatment, with those who receive standard NHS SSS treatment alone, will be measured by the Mood and Physical Symptoms Scale (MPSS; West & Hajek, 2004).
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Change in ratings of tobacco withdrawal symptoms, measured by the MPSS
Time Frame
First 4 weeks of abstinence (from baseline- 4 weeks post-quit)
Title
CO-validated continuous abstinence rates
Description
CO-validated continuous abstinence rates will be measured 1-4 weeks following the target quit day in the standard treatment condition and 1-4 weeks following cessation of DNCs in the DNC condition.
Time Frame
4-weeks
Title
Acceptability and user reactions to DNCs
Time Frame
2 weeks
Title
Urges to smoke 24 hours after quitting, measured by the MPSS
Time Frame
24 hours
Title
Profile of adverse effects up to 12 weeks post quitting
Time Frame
12 weeks
Title
Reactions to smoking cues
Description
The differences in reactions to smoking cues between the 2 groups will be measured with smoking-related images and by the Cue Exposure Subscale of the Wisconsin Inventory for Smoking Dependence (WISDM-68; Piper, et al., 2004).
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 18 years or over Seeking treatment to stop smoking Exclusion Criteria: Pregnant or breastfeeding Acute psychiatric illness
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hayden McRobbie
Organizational Affiliation
Queen Mary University of London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tobacco Dependence Research Unit
City
London
ZIP/Postal Code
E1 2JH
Country
United Kingdom

12. IPD Sharing Statement

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De-nicotinised Cigarettes Study

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