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NCT Number: NCT06020443

Adherence to Lung Cancer Screening by Low-dose Thoracic CT in Haut-Rhin Department, France.

The main objective of the study is to measure adherence to a lung cancer screening program using low-dose thoracic CT.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

50 year–74 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cabinet de médecine générale

Colmar, Haut-Rhin, 68000, France

About this study

Secondary objectives

  • To evaluate patient compliance over the entire duration of the screening program
  • To assess patient smoking cessation
  • To describe radiation doses received during CT scans
  • To identify organizational constraints for general practitioners
  • To compare stages at diagnosis before and after implementation of screening program

Conduct of research Eligible patients will be identified by general practitioners. Patients included will require a low-dose thoracic CT scan to be performed by a radiologist of their choice. Smoking cessation will be systematically proposed, and will be carried out by the general practitioner or a tobaccologist.

The radiation dose from thoracic CT scans should not exceed 100 mGy.cm Product Dose Length (i.e. < 1.5 mSv). Imaging reports will be forwarded to the general practitioner.

If the first CT scan is negative (T0): a second scan will be scheduled 1 year later (T1). If this second scan is also negative, in the absence of lung cancer risk factors other than smoking, scans will then be performed every two years. In the presence of a risk factor for lung cancer (other than tobacco), screening will remain annual.

In the event of a result classified as uncertain: a follow-up scan is scheduled at 3 months ; if the follow-up scan is negative, the next screening will be scheduled 1 year after this follow-up scan. If the screening performed 1 year later is also negative, subsequent screenings will be performed annually.

In the event of a positive result: the general practitioner will refer the patient to a pneumologist of his/her choice for further examinations; data from these additional examinations will be collected.

The screening protocol may evolve in line with recommendations issued by the French National Authority for Health (HAS).

For participants undergoing CT scan at the imaging department of Emile Muller hospital in Mulhouse (GHRMSA), a blood sample will be collected (optional) for subsequent biomarker assays.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients aged 50 to 74 years
  • Smoking OR having smoked (withdrawal of <15 years): ≥15 cigarettes/day for ≥25 years OR ≥10 cigarettes/day for ≥30 years
  • Affiliated or beneficiary of a social security scheme
  • Written informed consent

Exclusion criteria

  • Inability to walk up two flights of stairs without stopping
  • BMI > 35 kg/m²
  • Recent chest CT scan < 1 year
  • Personal history of lung cancer < 5 years or under treatment
  • Personal history of cancer being monitored by chest CT scan
  • Contraindication to lung cancer treatment or diagnostic investigations
  • Current or recent respiratory symptoms immediately suggestive of lung cancer
  • Pregnant or breast-feeding woman
  • Person under court protection, guardianship or curatorship
  • Person deprived of liberty by judicial or administrative decision.

Treatment and study plan

Low Dose chest CT Scan for Lung Cancer Screening

Procedure

Low dose CT scans will be performed for three years

Primary outcomes

  1. Rate of included patients having undergone the first screening scan

    Time frame: T0

Secondary outcomes

  1. Rate of patients who refused to participate in the screening program

    Time frame: 1 year

  2. Rate of included patients having completed CT scans at each stage of follow-up

    Time frame: 3 years

  3. Number of patients newly committed to smoking cessation during the screening period

    Time frame: 3 years

  4. Tobacco consumption

    Time frame: 3 years

  5. Radiation doses received at each CT scan

    Time frame: 3 years

  6. Organizational constraints of the screening program

    Time frame: before starting the study

    Organizational constraints of the screening program will be assessed on a subgroup of general practitioners by semi-structured interviews

  7. Stage at diagnosis (TNM classification) of patients with lung cancer

    Time frame: 3 years

    The stages at diagnosis of patients with lung cancer included in the study will be compared with those of undetected patients (data from the Haut-Rhin Cancer Registry).

Sponsors and collaborators

Lead sponsor

Groupe Hospitalier de la Region de Mulhouse et Sud Alsace

Other

Registry information

Acronym: DECANPHAR

Important dates

Study start
2023
Primary completion
2024
Study completion
2026
First posted
Aug 31, 2023
Registry last updated
May 8, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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