- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03527030
Cross-Sectional Survey on the Use of Tobacco Products - London (UK)
Cross Sectional Survey on the Use of Tobacco Products in the General Population and in Users of IQOS in London (2018-2020)
The main purpose of the research study is to estimate the prevalence of tobacco product use and describe the tobacco use patterns in adults in London, United Kingdom.
The study was prematurely terminated after the first annual survey and was not be repeated due to the impossibility to recruit sufficient participants to meet the target sample size in the IQOS user sample.
Study Overview
Status
Conditions
Detailed Description
The aim of the survey is to describe the current and past patterns of use of tobacco products in the general adult population of the Greater London area and in adult IQOS users registered in the IQOS user database of Philip Morris Limited (UK IQOS User Database), and explore their association with key independent variables. More specifically, the objectives are:
- Estimate the prevalence of current tobacco use status in the study population.
- Describe the past tobacco use status (cigarette, IQOS and other innovative products, including e-cigarettes) in the study population (i.e. never-use, initiation, product use transition, cessation, re-initiation, and relapse).
- Explore the association between self-reported health status and use of tobacco products in the study population.
- Explore the association between patterns of IQOS use including motivation to use, mis-use, satisfaction, and self-reported changes since switching to the product (in a number of domains where IQOS may have potential benefits), and consumer's satisfaction in the population of IQOS users in the Greater London area registered in UK IQOS User Database.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Vaud
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Lausanne, Vaud, Switzerland, 1007
- Philip Morris Products S.A.
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria (all participants, including IQOS users):
- Legally permitted to buy tobacco products in UK (≥18 years of age).
- Currently residing in the Greater London area.
- Able to read, write and understand English.
- Consent to participate in the survey
Inclusion Criteria (IQOS users only):
- Has used more than 100 HEETS tobacco sticks in his or her lifetime.
- Is currently using IQOS.
- Has access to the internet.
- Is not currently employed by Philip Morris International or any of its affiliates
Exclusion Criteria:
- Not meeting the inclusion criteria
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
General Population
Adults living in a registered household in the Greater London area.
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Face-to-face survey to estimate the prevalence of current tobacco use status in the general population of the Greater London area.
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IQOS users
Adult current IQOS users (at the time of survey) living in the Greater London area who are registered in the UK IQOS User Database and agree to be contacted for research purposes at the time of registration.
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Online survey to describe patterns of use in users of IQOS residing in the Greater London area.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Prevalence of current tobacco use
Time Frame: Study duration (1 year).
|
Prevalence of current tobacco use status in the study population.
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Study duration (1 year).
|
Past tobacco use status
Time Frame: Study duration (1 year).
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Past tobacco use status (cigarette, IQOS and other innovative products) in the study population.
|
Study duration (1 year).
|
Self-reported health status
Time Frame: Study duration (1 year).
|
Association between self-reported health status and use of tobacco products in the study population.
|
Study duration (1 year).
|
Perceived risk
Time Frame: Study duration (1 year).
|
Association between patterns of use with perceived risk.
|
Study duration (1 year).
|
IQOS use experience
Time Frame: Study duration (1 year).
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Describe the IQOS user experience, including motivation to use, mis-use, satisfaction, and self-reported changes since switching to the product (in a number of domains where IQOS may have potential benefits).
|
Study duration (1 year).
|
Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Pierpaolo Magnani, Philip Morris Products S.A.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- P1-PMX-04-UK
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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