SenRep: Sensorimotor Replacement With Electronic and De-nicotinised Cigarettes

Sponsor
Queen Mary University of London (Other)
Overall Status
Completed
CT.gov ID
NCT01414998
Collaborator
(none)
120
1
4
10
12

Study Details

Study Description

Brief Summary

There are currently two sensorimotor replacement products which may be of benefit in smoking cessation: de-nicotinised cigarettes (denics) and electronic cigarettes (ECs), and the purpose of this project is to investigate whether these replacements can help to alleviate tobacco withdrawal symptoms in smokers, during a period of abstinence. This project will be separated into two studies, following the same design and procedures.

Study 1 will seek to confirm the importance of sensorimotor cues by comparing the efficacy of a nicotine-free EC in alleviating withdrawal symptoms, to a behavioural distraction tool (e.g. stress ball) which provides no smoking-related cues.

Study 2 will investigate whether sensorimotor replacements which are more proximal to smoking (i.e. Denics), will be more effective in alleviating withdrawal symptoms than a replacement which only delivers some of the conditioned sensorimotor cues (i.e. ECs).

The investigators hypothesise that the EC will be more effective at reducing withdrawal symptoms compared to the stress ball in Study 1. In Study 2, it is hypothesised that the Denic will be more effective than the EC.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Stress Ball vs Nicotine-free E-Cigarette
  • Behavioral: Nicotine-free E-Cigarette vs De-nicotinised Cigarette
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Effect of Non-nicotine Sensorimotor Replacement on Withdrawal and Craving: Studies With Electronic and De-nicotinised Cigarettes
Study Start Date :
May 1, 2012
Actual Primary Completion Date :
Mar 1, 2013
Actual Study Completion Date :
Mar 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Stress Ball

This is the active comparator for study 1

Behavioral: Stress Ball vs Nicotine-free E-Cigarette
In a cross over design, participants will be randomly allocated to: use a stress ball for 5 minutes during a 1 hour controlled experiment. They will also use the stress ball for one day outside of the study centre. use a nicotine-free EC for 5 minutes during a 1 hour controlled experiment. They will also use the EC ad-libitum for one day outside of the study centre. One week later participants will complete the other arm.

Experimental: De-nicotinised Cigarette

This will be the experimental arm for study 2

Behavioral: Nicotine-free E-Cigarette vs De-nicotinised Cigarette
In a cross over design, participants will be randomly allocated to: use a nicotine-free EC for 5 minutes during a 1 hour controlled experiment. They will also use the EC ad-libitum for one day outside of the study centre. smoke 1 de-nicotinised cigarette during a 1 hour controlled experiment. They will also be given a pack to smoke ad-libitum for one day outside of the study centre. One week later participants will complete the other arm.

Experimental: Nicotine-free Electronic Cigarette (1)

This will be the experimental arm for study 1

Behavioral: Stress Ball vs Nicotine-free E-Cigarette
In a cross over design, participants will be randomly allocated to: use a stress ball for 5 minutes during a 1 hour controlled experiment. They will also use the stress ball for one day outside of the study centre. use a nicotine-free EC for 5 minutes during a 1 hour controlled experiment. They will also use the EC ad-libitum for one day outside of the study centre. One week later participants will complete the other arm.

Active Comparator: Nicotine-free Electronic Cigarette (2)

This will be the active comparator for study 2

Behavioral: Nicotine-free E-Cigarette vs De-nicotinised Cigarette
In a cross over design, participants will be randomly allocated to: use a nicotine-free EC for 5 minutes during a 1 hour controlled experiment. They will also use the EC ad-libitum for one day outside of the study centre. smoke 1 de-nicotinised cigarette during a 1 hour controlled experiment. They will also be given a pack to smoke ad-libitum for one day outside of the study centre. One week later participants will complete the other arm.

Outcome Measures

Primary Outcome Measures

  1. Urge to smoke at 10 minutes post product use [10 minutes]

    Urges to smoke will be measured at 10 minutes after use of products

Secondary Outcome Measures

  1. Tobacco withdrawal symptom ratings over 1 hour [1 hour]

    Change withdrawal ratings one hour after product use

  2. Tobacco withdrawal symptom ratings over one day [1 day]

    Change in tobacco withdrawal symptom ratings over a day

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • 18 years or over

  • Smokes at least 10 cigarettes per day

  • Smokes first cigarette within 1 hour of waking

Exclusion Criteria:
  • pregnant or breastfeeding

  • acute psychiatric illness

  • currently enrolled in other research projects

  • current use of ECs or Denics

Contacts and Locations

Locations

Site City State Country Postal Code
1 Tobacco Dependence Research Unit London United Kingdom E1 2JH

Sponsors and Collaborators

  • Queen Mary University of London

Investigators

  • Principal Investigator: Dunja Przulj, Queen Mary University of London

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dunja Przulj, Prinicipal Investigator, Queen Mary University of London
ClinicalTrials.gov Identifier:
NCT01414998
Other Study ID Numbers:
  • qmul1606
First Posted:
Aug 11, 2011
Last Update Posted:
Mar 20, 2013
Last Verified:
Mar 1, 2013
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 20, 2013