Actively Recruiting
Targeted Abdominal CT in Conjunction With Lung Cancer Screening - a Pilot Study (TACTICAL1): a Randomised Controlled Pilot Study of Adding Abdominal Non-contrast CT to Lung Cancer Screening CT Thorax Amongst High Lung Cancer Risk Ever-smokers Aged 55-70.
Led by University of Cambridge · Updated on 2025-12-19
6272
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
U
University of Cambridge
Lead Sponsor
H
Hull University Teaching Hospitals NHS Trust
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the addition of an abdominal CT scan to the existing Lung Cancer Screening (LCS) program for people aged 55 to 70 who have ever smoked. This study aims to see if mentioning the abdominal scan in the initial LCS invitation affects participation, test new ways to add the abdominal scan without causing delays, and assess if participants can be assigned to different scan groups using cluster randomisation. The research focuses on the feasibility and acceptability of combining these scans in lung cancer screening centers in Yorkshire. Participants will be invited to the NHS Lung Cancer Screening via letter or text message. Those at high risk for lung cancer based on risk models will be offered a lung scan, and some will be invited to have an abdominal CT scan at the same time. The study compares groups receiving the standard invitation with those also informed about the possible abdominal scan and evaluates the impact on scheduling and participant experience. This approach includes two study arms for invitation and scan procedures. During the study, participants' attendance at screening assessments will be tracked along with the time taken for additional tasks related to the abdominal scan. Satisfaction with the scanning experience will be measured, and uptake of the abdominal scan offer will be recorded. Follow-up will occur up to six months after invitation, and data will be collected on the process and impact of adding the abdominal scan alongside lung screening. Participants will be monitored for safety and acceptability throughout the study period.
CONDITIONS
Brief Title
Targeted Abdominal CT in Conjunction With Lung Cancer Screening
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Be eligible to be invited to the first round of a West Yorkshire and Harrogate or Humber and North Yorkshire Lung Cancer Screening program
- Be identified as a smoker or ex-smoker
- Be registered with a general practitioner in England
- Be aged between 55 and 70 years 364 days at the date of invitation
- Have been individually randomised to the invitation intervention arm and booked for a Lung Cancer Screening assessment
- Be invited for a lung scan based on risk prediction models and attend the lung scan appointment
- Provide electronic or written informed consent to participate
You will not qualify if you...
- Lack capacity to give consent
- Weight or physical size exceeds scanner limits (over 200kg)
- Unable to lie flat for scanning
- Poor physical fitness making curative treatment unsuitable
- Had a full CT Thorax meeting program standards in the last 12 months and appointment deferred beyond trial time frame
- Had an abdominal CT scan in the last 12 months or have one scheduled in the next 3 months
AI-Screening
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Your Study Journey
Duration - Up to 12 weeks
Participants are screened for eligibility to participate in the trial.
1 invitation and assessment visit
Duration - Up to 6 months after invitation
Participants undergo lung cancer screening and, if eligible and randomized, may receive an additional abdominal CT scan at the same time.
1 combined lung and abdominal CT scan visit for those eligible
Duration - Up to 6 months after invitation
Participants are followed up to assess attendance, satisfaction, and impact of the abdominal scan on screening throughput.
Follow-up assessments conducted remotely or via phone
Trial Site Locations
Total: 1 location
1
Hull Teaching Hospitals Trust
Hull, United Kingdom, HU3 2JZ
Actively Recruiting
Research Team
G
Grant Stewart
J
Jessica Kitt
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SCREENING
Number of Arms
4
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