Cancer, LungYESSNCT03750110
Yorkshire Enhanced Stop Smoking Study
A study testing Intervention in people with Cancer, Lung and Respiratory Disease, run by University of Nottingham at 1 site in United Kingdom.
Trial summary
Lung cancer rates are higher in Yorkshire than the rest of the UK, and this is due to higher rates of smoking. Deaths from lung cancer can be reduced using regular lung scans (screening) and by helping people stop smoking. Read more about this study
- Who is it for?
- Ages 55 to 80 years, men only
- Conditions the study is for
- Cancer, Lung, Respiratory Disease, Heart Diseases
- What is being tested?
- Intervention
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,001 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 1 Jul 2017to 21 Mar 2022
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 55 to 80 years
- Men only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Residing in the newly merged Leeds South \& East, Leeds West or Leeds North CCG
- Registered as a current or ex-smoker in a General Practice participating in YLST
- Have attended for a 'Lung Health Check' and agreed to see the SCP as part of YLST
- Smoked within the last month or have exhaled CO reading of 6ppm or above.
- Have capacity to provide informed consent.
Who cannot join
None listed.
Trial locations and contacts
1 site in 1 country.
United Kingdom1 site
Leeds Teaching Hospitals NHS Trust
Leeds, West Yorkshire, LS9 7TF
About this study
Official title: The Effect of Adding a Personalised Smoking Cessation Intervention to a Lung Cancer Screening Programme
Lung cancer rates are higher in Yorkshire than the rest of the UK, and this is due to higher rates of smoking. Deaths from lung cancer can be reduced using regular lung scans (screening) and by helping people stop smoking. As well as detecting cancers, scans can also show evidence of damage to lungs (emphysema) and heart arteries (calcification). This study will test whether people can be encouraged to quit smoking by giving them pictures from their own scans showing possible lung and heart damage, along with information about how stopping smoking reduces their risk of cancer and heart attacks.
Read the detailed description
Lung cancer has the highest mortality of all cancers in the UK and is the single biggest cause of premature death in Leeds. It disproportionately affects those from lower socioeconomically deprived communities where rates of smoking are highest. In 2014 in the Leeds South and East and the Leeds West Clinical Commissioning Group (CCG) areas, lung cancer standardized incidence rates were 131.4 and 103.3 respectively, compared to an average of 78.3 across England. Lung cancer standardized under-75 mortality rates were 52.4 and 39.3 respectively, compared to 33.26 across England. Poor outcomes from lung cancer treatment are typically the result of advanced, incurable disease at the time of symptomatic presentation. In 2011, the US National Lung Screening Trial (NLST) demonstrated a 20% reduction in lung cancer specific mortality, and a 6.7% reduction in all-cause mortality by annual low-dose CT (LDCT) screening, and lung cancer screening is now being adopted across North America having been recommended by the US Preventative Services Task Force (USPSTF) in 2013. A number of European nations are deliberating introducing screening programmes for lung cancer, and await the results of the NELSON study, the only European study powered to demonstrate a mortality reduction, which remains in follow-up. Despite widespread adoption in North America, several important questions remain regarding the best way to implement lung cancer screening. These include the optimum selection criteria to identify high-risk individuals to maximise clinical efficacy and cost-effectiveness, how to increase participation among 'hard to reach' populations, and how most effectively to embed smoking cessation support into these programmes. The Yorkshire Lung Screening Trial, funded by Yorkshire Cancer Research ( ISRCTN reference number 42704678) , seeks to address the first two issues identified above, and is due to commence screening in 2018. However, there are no currently funded UK studies specifically investigating optimal smoking cessation provision within a lung cancer screening programme.
More than 85% of cases of lung cancer are caused by tobacco smoking, and stopping smoking, at any age, significantly reduces lung cancer risk. It is therefore essential that any lung cancer screening programme provides smoking cessation support for participants, and doing so significantly increases the overall success of lung cancer screening programmes. One concern that has been raised around lung cancer screening for current smokers is the potential 'moral hazard' arising from a negative (i.e. reassuring) screening result, which may reduce motivation to quit. Conversely, attendance at a lung cancer screening programme offers a 'teachable moment' for smoking cessation, occurring at a time when participating smokers may be particularly receptive to offers of help to quit and indeed a negative screen result has been reported as being perceived as a 'clean slate' as a motivator to stop smoking. This observation fits with unpublished findings from a screening initiative in Manchester that despite a high prevalence of emphysema (68%) and coronary artery calcification (74%), most attendees were fit and relatively asymptomatic (85-90% performance status 0-1 and MRC dyspnoea scale 1-2), and hence potentially more susceptible to a message that lung damage had already occurred but clinical impact could be reduced by stopping smoking. One report from the NELSON study suggested a lower quit rate in screened persons compared to the unscreened control group, although a statistically significant effect did not persist following intention to treat analysis. No significant difference was seen between screened and control populations in the Danish Lung Cancer Screening Study, and the quit rate was significantly higher in screened versus control populations in the UK Lung Screening (UKLS) Pilot. Evidence suggests that smoking cessation and LDCT screening have additive effects on survival. An analysis of participants in the NLST reported a 38% reduction in lung cancer mortality with the combination of smoking abstinence at 15 years with LDCT screening; in addition, detection of an abnormality on the CT scan was associated with increased likelihood of smoking cessation. Further analysis of the NLST showed that arranging the smoking cessation support at the time of the screening increased quit rates by 46% (although this intervention was delivered to only 10% of study participants). In addition, research has indicated that adding smoking cessation interventions to LDCT screening improves the cost effectiveness of such programmes.
However, while smoking cessation is clearly an effective preventive intervention there is little evidence on the design and optimization of the smoking cessation interventions and support used in the screening setting. Evidence from a systematic review published in 2014 showed a benefit of materials tailored to the characteristics of individual smokers, although the included studies were conducted predominantly in the general population, rather than screening participants. Less research has been conducted investigating approaches to cessation in smokers attending for lung cancer screening, although a recent study by Marshall and colleagues reported that it was feasible to deliver a single tailored session of motivational interviewing counselling on the day of screening. For historical reasons NHS Stop Smoking Services (SSS) have evolved across the UK as opt-in facilities, whereby smokers who decide or agree to try to quit smoking then seek and are delivered help to do so. During the past five years however, evidence has grown that provision of smoking cessation support as an opt-out default generates far more quit attempts. We have demonstrated this to be the case in hospital inpatients, in which the opt-out model approximately doubled service uptake. Similar findings have been reported in relation to pregnant women setting quit dates in one NHS Foundation Trust, with uptake more than doubling after 'opt out' referrals were implemented. A study from the US found that 83% of eligible smokers did not opt out of a bedside consultation. Pro-active and systematic approaches to smoking cessation provision were recommended by NICE for pregnant women in 2010 and across all acute, maternity and mental health settings in 2013.
A recent UK study has also demonstrated the efficacy of including personalised risk information when inviting participants to smoking cessation services. A randomised controlled trial compared an individually tailored risk letter with an invitation to attend an introductory smoking cessation session to a standard generic letter advertising smoking cessation services. The personalised information was presented as a "Personal Health Risk Report", and included information on the participant's general health derived from Quality and Outcomes Framework (QOF) registered conditions on the GP record. In addition disease-specific health risks were included in the risk report, with the aim of making the individual aware of the personal health consequences of continuing to smoke, and their own individual risk of serious illness. The aim of providing this information was to change the individual's balance of perceived 'benefits' against their understanding of the harm caused by smoking. The group receiving personalised risk information had significantly higher attendance at stop smoking service (17.4% vs. 9.0%, adjusted OR 2.2, 95% CI 1.8- 2.7), higher completion of a 6-week NHS course (14.5% vs. 7.0%, adjusted OR 2.3, 95% CI 1.8-2.9) and higher 6- month validated abstinence (9.0% vs. 5.5%, adjusted OR 1.67, 95% CI 1.29-2.14).
To maximize smoking cessation among lung cancer screening participants it is therefore clearly important that all smokers who attend are provided with cessation support as a routine opt-out component of the screening visit, and that this support provides cessation pharmacotherapy and behavioural support in accordance with evidence-based NHS SSS practice. Furthermore the screening process, including risk assessment for lung cancer and imaging of the lung parenchyma and coronary arteries, allows an unprecedented opportunity for personalising the risks and harms of continued smoking, or conversely, the health gains to be made by successful smoking cessation. However there is currently no evidence on how best to design services to maximize the opportunity provided by screening participation, and how best to use the personalised information forthcoming from the screening process.
- Conditions
- Cancer, Lung, Respiratory Disease, Heart Diseases
- Being tested
- Intervention, Usual Care
- Medical subject headings
- Lung Neoplasms, Respiration Disorders, Heart Diseases
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
InterventionOther
In addition to usual care, personalised feedback from the participants screening appointment will be provided;
- For participants with emphysema, an image of their own emphysematous lung compared to a library image of normal lung, or a section of their own non-emphysematous lung. Where emphysema is not present, library pictures showing normal and emphysematous lung will be used.
- For participants with coronary artery calcification, a cross sectional segment from their chest scan (either horizontal or vertical) showing the calcium compared to a library image of coronary arteries without calcification and/or a healthy section of the participant's own heart scan. Where coronary artery calcification is not present, library pictures showing normal and calcified coronary arteries will be provided.
Usual CareOther
Smoking cessation support in line with NICE PH48 guidelines
| Study group | Role | What they receive |
|---|---|---|
| Usual Care | Active comparator | Smoking Cessation NICE PH48 Guidelines Receives: Other: Usual Care |
| Intervention | Active comparator | Smoking Cessation NICE PH48 Guidelines plus personalised feedback from Lung Scan Receives: Other: Intervention |
What is being measured
The primary outcome is the main question the study is designed to answer.
7-day point prevalent CO validated smoking cessation.
Exhaled Carbon Monoxide reading of 6ppm or less to validate smoking cessation
Measured: Three months after lung screening
Secondary outcomes (20)
Self-reported continuous smoking cessation at three months
Participant self-report being quit continuously for three months after Lung Screening. Binary question " Have you smoked in the 3 months since Lung Screening, yes or no?"
Measured: Three months after lung screening
Self-reported continuous cessation at 12 months
Participant self-reports being quit continuously for 12 months following Lung Screening. Binary question " Have you smoked in the 12 months since Lung Screening, yes or no?"
Measured: 12 months after Lung Screening
CO validated cessation at 12 months
Exhaled Carbon Monoxide reading of 6ppm or less to validate smoking cessation
Measured: 12 Months after lung screening
Self-reported continuous cessation at 4 weeks
Participant self-reports being quit continuously for 4 weeks following Lung Screening. Binary question " Have you smoked in the 4 weeks since Lung Screening, yes or no?"
Measured: four weeks after lung screening
CO validated cessation at 4 weeks
Exhaled Carbon Monoxide reading of 6ppm or less to validate smoking cessation
Measured: four weeks after lung screening
Changes in perceived risk of lung cancer
Cancer worry score (UKLS adapted version)
Measured: 4 weeks after lung screening
Changes in perceived risk of lung cancer
Cancer worry score (UKLS adapted version)
Measured: 3 months after lung screening
Changes in perceived risk of lung cancer
Cancer worry score (UKLS adapted version)
Measured: 12 months after lung screening
Changes in motivation to quit smoking tobacco
Motivation to stop smoking - questionnaire
Measured: 12 months after lung screening
Changes in motivation to quit smoking tobacco
Motivation to stop smoking - questionnaire
Measured: 3 months after lung screening
Changes in motivation to quit smoking tobacco
Motivation to stop smoking - questionnaire
Measured: 4 weeks after lung screening
Changes in confidence and efficacy beliefs of stopping smoking
Response efficacy (of stopping smoking) - questionnaire
Measured: 12 months after lung screening
Changes in confidence and efficacy beliefs of stopping smoking
Response efficacy (of stopping smoking) - questionnaire
Measured: 3 months after lung screening
Changes in confidence and efficacy beliefs of stopping smoking
Response efficacy (of stopping smoking) - questionnaire
Measured: 4 weeks after lung health screening
Confidence and efficacy beliefs of stopping smoking
Self efficacy (of stopping smoking) - Questionnaire
Measured: 4 weeks after lung screening
Confidence and efficacy beliefs of stopping smoking
Self efficacy (of stopping smoking) - Questionnaire
Measured: 3 months after lung screening
Confidence and efficacy beliefs of stopping smoking
Self efficacy (of stopping smoking) - Questionnaire
Measured: 12 months after lung screening
Self -reported changes in health
Health questionnaire (EQ-5D-5L)
Measured: 3 months after lung screening
Self -reported changes in health
Health questionnaire (EQ-5D-5L)
Measured: 12 months after lung screening
7-day point prevalent self reported smoking cessation at 3 months
Exhaled Carbon Monoxide reading of 6ppm or less to validate smoking cessation
Measured: Three months after lung screening
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Nov 2018
- Study start1 Jul 2017
- Primary completion21 Mar 2022
- Study completion21 Mar 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Cancer, LungStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- The study will use a pragmatic, parallel-group, open, randomized controlled trial design
- Masking
- None (open label)
- Enrolment
- 1,001 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Nottingham
- Sponsor type
- University, hospital or other
- Collaborators
- The Leeds Teaching Hospitals NHS Trust, University of Leeds, Cardiff University, University of Manchester, University College, London, University of York, Yorkshire Cancer Research
- Responsible party
- Sponsor
- Investigators
- Rachael L Murray, BSc MS MSc PhD, Principal investigator, University of NottinghamMatthew Callister, MA, BM BCh, MEd, FRCP, PhD, Principal investigator, The Leeds Teaching Hospitals NHS Trust
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT03750110
- Sponsor's protocol ID
- 18046
- Acronym
- YESS
- Status last verified
- Sep 2020
- First submitted
- 17 Sep 2018
- Last updated
- 19 May 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Murray RL, Baldwin D, Brain K, Britton J, Chalitsios CV, Crosbie PA, Lewis S, McCutchan G, Steve P, Quaife S, Thorley R, Wu Q, Ashurst A, Beeken RJ, Copeland H, Gabe R, Hancock N, Marshall CS, Neal RD, Porter LR, Rogerson S, Quinn-Scoggins HD, Simmonds I, Sloss A, Callister MEJ. Randomised trial of delivering co-located, personalised stop-smoking support within lung cancer screening: the YESS study. Thorax. 2026 Mar 13:thorax-2025-224217. doi: 10.1136/thorax-2025-224217. Online ahead of print.
PubMed 41825863McInnerney D, Simmonds I, Hancock N, Rogerson S, Lindop J, Gabe R, Vulkan D, Marshall C, Crosbie PAJ, Callister MEJ, Quaife SL. Yorkshire Lung Screening Trial (YLST) pathway navigation study: a protocol for a nested randomised controlled trial to evaluate the effect of a pathway navigation intervention on lung cancer screening uptake. BMJ Open. 2024 Jul 9;14(7):e084577. doi: 10.1136/bmjopen-2024-084577.
PubMed 38986555Murray RL, Brain K, Britton J, Quinn-Scoggins HD, Lewis S, McCutchan GM, Quaife SL, Wu Q, Ashurst A, Baldwin D, Crosbie PAJ, Neal RD, Parrott S, Rogerson S, Thorley R, Callister ME. Yorkshire Enhanced Stop Smoking (YESS) study: a protocol for a randomised controlled trial to evaluate the effect of adding a personalised smoking cessation intervention to a lung cancer screening programme. BMJ Open. 2020 Sep 10;10(9):e037086. doi: 10.1136/bmjopen-2020-037086.
PubMed 32912948Crosbie PA, Gabe R, Simmonds I, Kennedy M, Rogerson S, Ahmed N, Baldwin DR, Booton R, Cochrane A, Darby M, Franks K, Hinde S, Janes SM, Macleod U, Messenger M, Moller H, Murray RL, Neal RD, Quaife SL, Sculpher M, Tharmanathan P, Torgerson D, Callister ME. Yorkshire Lung Screening Trial (YLST): protocol for a randomised controlled trial to evaluate invitation to community-based low-dose CT screening for lung cancer versus usual care in a targeted population at risk. BMJ Open. 2020 Sep 10;10(9):e037075. doi: 10.1136/bmjopen-2020-037075.
PubMed 32912947
Study at a glance
From the registry record, last updated by the sponsor on 19 May 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Adding a Personalised Smoking Cessation Intervention to a Lung Cancer Screening Programme
- ClinicalTrials.gov ID
- NCT03750110
- Acronym / sponsor ID
- YESS / 18046
- Conditions
- Cancer, Lung, Respiratory Disease, Heart Diseases
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 1,001 participants (actual)
- Lead sponsor
- University of NottinghamUniversity, hospital or other
- Collaborators
- The Leeds Teaching Hospitals NHS Trust, University of Leeds, Cardiff University, University of Manchester, University College, London, University of York, Yorkshire Cancer Research
- Study start
- 1 Jul 2017 (actual)
- Primary completion
- 21 Mar 2022 (actual)
- Study completion
- 21 Mar 2022 (actual)
- First posted
- 21 Nov 2018 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Lung cancer rates are higher in Yorkshire than the rest of the UK, and this is due to higher rates of smoking. Deaths from lung cancer can be reduced using regular lung scans (screening) and by helping people stop smoking. As well as detecting cancers, scans can also show evidence of damage to lungs (emphysema) and heart arteries (calcification). This study will test whether people can be encouraged to quit smoking by giving them pictures from their own scans showing possible lung and heart damage, along with information about how stopping smoking reduces their risk of cancer and heart attacks.
Detailed description
Lung cancer has the highest mortality of all cancers in the UK and is the single biggest cause of premature death in Leeds. It disproportionately affects those from lower socioeconomically deprived communities where rates of smoking are highest. In 2014 in the Leeds South and East and the Leeds West Clinical Commissioning Group (CCG) areas, lung cancer standardized incidence rates were 131.4 and 103.3 respectively, compared to an average of 78.3 across England. Lung cancer standardized under-75 mortality rates were 52.4 and 39.3 respectively, compared to 33.26 across England. Poor outcomes from lung cancer treatment are typically the result of advanced, incurable disease at the time of symptomatic presentation. In 2011, the US National Lung Screening Trial (NLST) demonstrated a 20% reduction in lung cancer specific mortality, and a 6.7% reduction in all-cause mortality by annual low-dose CT (LDCT) screening, and lung cancer screening is now being adopted across North America having been recommended by the US Preventative Services Task Force (USPSTF) in 2013. A number of European nations are deliberating introducing screening programmes for lung cancer, and await the results of the NELSON study, the only European study powered to demonstrate a mortality reduction, which remains in follow-up. Despite widespread adoption in North America, several important questions remain regarding the best way to implement lung cancer screening. These include the optimum selection criteria to identify high-risk individuals to maximise clinical efficacy and cost-effectiveness, how to increase participation among 'hard to reach' populations, and how most effectively to embed smoking cessation support into these programmes. The Yorkshire Lung Screening Trial, funded by Yorkshire Cancer Research ( ISRCTN reference number 42704678) , seeks to address the first two issues identified above, and is due to commence screening in 2018. However, there are no currently funded UK studies specifically investigating optimal smoking cessation provision within a lung cancer screening programme.
More than 85% of cases of lung cancer are caused by tobacco smoking, and stopping smoking, at any age, significantly reduces lung cancer risk. It is therefore essential that any lung cancer screening programme provides smoking cessation support for participants, and doing so significantly increases the overall success of lung cancer screening programmes. One concern that has been raised around lung cancer screening for current smokers is the potential 'moral hazard' arising from a negative (i.e. reassuring) screening result, which may reduce motivation to quit. Conversely, attendance at a lung cancer screening programme offers a 'teachable moment' for smoking cessation, occurring at a time when participating smokers may be particularly receptive to offers of help to quit and indeed a negative screen result has been reported as being perceived as a 'clean slate' as a motivator to stop smoking. This observation fits with unpublished findings from a screening initiative in Manchester that despite a high prevalence of emphysema (68%) and coronary artery calcification (74%), most attendees were fit and relatively asymptomatic (85-90% performance status 0-1 and MRC dyspnoea scale 1-2), and hence potentially more susceptible to a message that lung damage had already occurred but clinical impact could be reduced by stopping smoking. One report from the NELSON study suggested a lower quit rate in screened persons compared to the unscreened control group, although a statistically significant effect did not persist following intention to treat analysis. No significant difference was seen between screened and control populations in the Danish Lung Cancer Screening Study, and the quit rate was significantly higher in screened versus control populations in the UK Lung Screening (UKLS) Pilot. Evidence suggests that smoking cessation and LDCT screening have additive effects on survival. An analysis of participants in the NLST reported a 38% reduction in lung cancer mortality with the combination of smoking abstinence at 15 years with LDCT screening; in addition, detection of an abnormality on the CT scan was associated with increased likelihood of smoking cessation. Further analysis of the NLST showed that arranging the smoking cessation support at the time of the screening increased quit rates by 46% (although this intervention was delivered to only 10% of study participants). In addition, research has indicated that adding smoking cessation interventions to LDCT screening improves the cost effectiveness of such programmes.
However, while smoking cessation is clearly an effective preventive intervention there is little evidence on the design and optimization of the smoking cessation interventions and support used in the screening setting. Evidence from a systematic review published in 2014 showed a benefit of materials tailored to the characteristics of individual smokers, although the included studies were conducted predominantly in the general population, rather than screening participants. Less research has been conducted investigating approaches to cessation in smokers attending for lung cancer screening, although a recent study by Marshall and colleagues reported that it was feasible to deliver a single tailored session of motivational interviewing counselling on the day of screening. For historical reasons NHS Stop Smoking Services (SSS) have evolved across the UK as opt-in facilities, whereby smokers who decide or agree to try to quit smoking then seek and are delivered help to do so. During the past five years however, evidence has grown that provision of smoking cessation support as an opt-out default generates far more quit attempts. We have demonstrated this to be the case in hospital inpatients, in which the opt-out model approximately doubled service uptake. Similar findings have been reported in relation to pregnant women setting quit dates in one NHS Foundation Trust, with uptake more than doubling after 'opt out' referrals were implemented. A study from the US found that 83% of eligible smokers did not opt out of a bedside consultation. Pro-active and systematic approaches to smoking cessation provision were recommended by NICE for pregnant women in 2010 and across all acute, maternity and mental health settings in 2013.
A recent UK study has also demonstrated the efficacy of including personalised risk information when inviting participants to smoking cessation services. A randomised controlled trial compared an individually tailored risk letter with an invitation to attend an introductory smoking cessation session to a standard generic letter advertising smoking cessation services. The personalised information was presented as a "Personal Health Risk Report", and included information on the participant's general health derived from Quality and Outcomes Framework (QOF) registered conditions on the GP record. In addition disease-specific health risks were included in the risk report, with the aim of making the individual aware of the personal health consequences of continuing to smoke, and their own individual risk of serious illness. The aim of providing this information was to change the individual's balance of perceived 'benefits' against their understanding of the harm caused by smoking. The group receiving personalised risk information had significantly higher attendance at stop smoking service (17.4% vs. 9.0%, adjusted OR 2.2, 95% CI 1.8- 2.7), higher completion of a 6-week NHS course (14.5% vs. 7.0%, adjusted OR 2.3, 95% CI 1.8-2.9) and higher 6- month validated abstinence (9.0% vs. 5.5%, adjusted OR 1.67, 95% CI 1.29-2.14).
To maximize smoking cessation among lung cancer screening participants it is therefore clearly important that all smokers who attend are provided with cessation support as a routine opt-out component of the screening visit, and that this support provides cessation pharmacotherapy and behavioural support in accordance with evidence-based NHS SSS practice. Furthermore the screening process, including risk assessment for lung cancer and imaging of the lung parenchyma and coronary arteries, allows an unprecedented opportunity for personalising the risks and harms of continued smoking, or conversely, the health gains to be made by successful smoking cessation. However there is currently no evidence on how best to design services to maximize the opportunity provided by screening participation, and how best to use the personalised information forthcoming from the screening process.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
- Model description
- The study will use a pragmatic, parallel-group, open, randomized controlled trial design
| Arm | Type | Receives |
|---|---|---|
| Usual Care | Active comparator | Other: Usual CareSmoking Cessation NICE PH48 Guidelines |
| Intervention | Active comparator | Other: InterventionSmoking Cessation NICE PH48 Guidelines plus personalised feedback from Lung Scan |
Who may qualify
- Ages
- 55 to 80 years
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Residing in the newly merged Leeds South \& East, Leeds West or Leeds North CCG
- Registered as a current or ex-smoker in a General Practice participating in YLST
- Have attended for a 'Lung Health Check' and agreed to see the SCP as part of YLST
- Smoked within the last month or have exhaled CO reading of 6ppm or above.
- Have capacity to provide informed consent.
Key exclusion criteria (0 listed)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| InterventionIn addition to usual care, personalised feedback from the participants screening appointment will be provided; * For participants with emphysema, an image of their own emphysematous lung compared to a library image of normal lung, or a section of their own non-emphysematous lung. Where emphysema is not present, library pictures showing normal and emphysematous lung will be used. * For participants with coronary artery calcification, a cross sectional segment from their chest scan (either horizontal or vertical) showing the calcium compared to a library image of coronary arteries without calcification and/or a healthy section of the participant's own heart scan. Where coronary artery calcification is not present, library pictures showing normal and calcified coronary arteries will be provided. | Other | Intervention |
| Usual CareSmoking cessation support in line with NICE PH48 guidelines | Other | Usual Care |
Primary outcome
7-day point prevalent CO validated smoking cessation.
Time frame: Three months after lung screening
Exhaled Carbon Monoxide reading of 6ppm or less to validate smoking cessation
20 secondary outcomes
Self-reported continuous smoking cessation at three months
Time frame: Three months after lung screening
Self-reported continuous cessation at 12 months
Time frame: 12 months after Lung Screening
CO validated cessation at 12 months
Time frame: 12 Months after lung screening
Self-reported continuous cessation at 4 weeks
Time frame: four weeks after lung screening
CO validated cessation at 4 weeks
Time frame: four weeks after lung screening
Changes in perceived risk of lung cancer
Time frame: 4 weeks after lung screening
Changes in perceived risk of lung cancer
Time frame: 3 months after lung screening
Changes in perceived risk of lung cancer
Time frame: 12 months after lung screening
Changes in motivation to quit smoking tobacco
Time frame: 12 months after lung screening
Changes in motivation to quit smoking tobacco
Time frame: 3 months after lung screening
Changes in motivation to quit smoking tobacco
Time frame: 4 weeks after lung screening
Changes in confidence and efficacy beliefs of stopping smoking
Time frame: 12 months after lung screening
Changes in confidence and efficacy beliefs of stopping smoking
Time frame: 3 months after lung screening
Changes in confidence and efficacy beliefs of stopping smoking
Time frame: 4 weeks after lung health screening
Confidence and efficacy beliefs of stopping smoking
Time frame: 4 weeks after lung screening
Confidence and efficacy beliefs of stopping smoking
Time frame: 3 months after lung screening
Confidence and efficacy beliefs of stopping smoking
Time frame: 12 months after lung screening
Self -reported changes in health
Time frame: 3 months after lung screening
Self -reported changes in health
Time frame: 12 months after lung screening
7-day point prevalent self reported smoking cessation at 3 months
Time frame: Three months after lung screening
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 19 May 2022.
- Derived from this study: PubMed 41825863Murray RL, Baldwin D, Brain K, Britton J, Chalitsios CV, Crosbie PA, Lewis S, McCutchan G, Steve P, Quaife S, Thorley R, Wu Q, Ashurst A, Beeken RJ, Copeland H, Gabe R, Hancock N, Marshall CS, Neal RD, Porter LR, Rogerson S, Quinn-Scoggins HD, Simmonds I, Sloss A, Callister MEJ. Randomised trial of delivering co-located, personalised stop-smoking support within lung cancer screening: the YESS study. Thorax. 2026 Mar 13:thorax-2025-224217. doi: 10.1136/thorax-2025-224217. Online ahead of print.
- Derived from this study: PubMed 38986555McInnerney D, Simmonds I, Hancock N, Rogerson S, Lindop J, Gabe R, Vulkan D, Marshall C, Crosbie PAJ, Callister MEJ, Quaife SL. Yorkshire Lung Screening Trial (YLST) pathway navigation study: a protocol for a nested randomised controlled trial to evaluate the effect of a pathway navigation intervention on lung cancer screening uptake. BMJ Open. 2024 Jul 9;14(7):e084577. doi: 10.1136/bmjopen-2024-084577.
- Derived from this study: PubMed 32912948Murray RL, Brain K, Britton J, Quinn-Scoggins HD, Lewis S, McCutchan GM, Quaife SL, Wu Q, Ashurst A, Baldwin D, Crosbie PAJ, Neal RD, Parrott S, Rogerson S, Thorley R, Callister ME. Yorkshire Enhanced Stop Smoking (YESS) study: a protocol for a randomised controlled trial to evaluate the effect of adding a personalised smoking cessation intervention to a lung cancer screening programme. BMJ Open. 2020 Sep 10;10(9):e037086. doi: 10.1136/bmjopen-2020-037086.
- Derived from this study: PubMed 32912947Crosbie PA, Gabe R, Simmonds I, Kennedy M, Rogerson S, Ahmed N, Baldwin DR, Booton R, Cochrane A, Darby M, Franks K, Hinde S, Janes SM, Macleod U, Messenger M, Moller H, Murray RL, Neal RD, Quaife SL, Sculpher M, Tharmanathan P, Torgerson D, Callister ME. Yorkshire Lung Screening Trial (YLST): protocol for a randomised controlled trial to evaluate invitation to community-based low-dose CT screening for lung cancer versus usual care in a targeted population at risk. BMJ Open. 2020 Sep 10;10(9):e037075. doi: 10.1136/bmjopen-2020-037075.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Rachael L Murray, BSc MS MSc PhD principal investigator
University of Nottingham
Matthew Callister, MA, BM BCh, MEd, FRCP, PhD principal investigator
The Leeds Teaching Hospitals NHS Trust
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Intervention in people with Cancer, Lung and Respiratory Disease, run by University of Nottingham at 1 site in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 19 May 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
7-day point prevalent CO validated smoking cessation. (time frame: Three months after lung screening). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT03750110, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 19 May 2022.