Assessment of Tobacco Smoking and Alcohol Drinking and Treatment Outcomes Among Patients With Lung or Head and Neck Cancer

NCT ID: NCT05523583

Last Updated: 2025-10-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

165 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-10-27

Study Completion Date

2025-09-18

Brief Summary

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The overarching goal of the proposed study is to provide information which can lead to effective implementation of cessation support in the care of smokers diagnosed with lung or head \& neck cancer.

To achieve these aims, the study propose to conduct a longitudinal cohort study of patients diagnosed with lung or head \& neck cancer at the Hospices Civils de Lyon (SMALLHAN). Briefly, adult patients newly diagnosed with lung or head \& neck cancer will be recruited at the time of diagnosis (announcement of diagnosis and consultation).

Detailed Description

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Conditions

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Lung or Head and Neck Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Patients newly diagnosed with lung cancer or head & neck cancer

Patients newly diagnosed with lung cancer or head \& neck cancer (International Classification of Diseases 10: C76, C34) who undergo front-line treatment and who had at least one episode of smoking within the past 30 days before diagnosis

questionnaire

Intervention Type OTHER

A trained interviewer (Clinical Research Associate : CRA) will administer a questionnaire soon after the diagnosis on the phone (within 15 calendar days after diagnosis). The participants are followed up during the first year following the diagnosis through 3 follow-up assessments (at 3, 6, and 12 months after the baseline assessment) and hospital record reviews. At each follow-up, a brief questionnaire will be administered by an interviewer (CRA) via telephone.

Interventions

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questionnaire

A trained interviewer (Clinical Research Associate : CRA) will administer a questionnaire soon after the diagnosis on the phone (within 15 calendar days after diagnosis). The participants are followed up during the first year following the diagnosis through 3 follow-up assessments (at 3, 6, and 12 months after the baseline assessment) and hospital record reviews. At each follow-up, a brief questionnaire will be administered by an interviewer (CRA) via telephone.

Intervention Type OTHER

Other Intervention Names

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Tabacco and alcohol questionnaires

Eligibility Criteria

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Inclusion Criteria

* Patients newly diagnosed with lung cancer or head \& neck cancer (International Classification of Diseases 10: C76, C34)
* Patients who undergo front-line treatment
* Age 18 years or older
* Benefiting from a Social Security scheme
* Written information about the study provided to the patient before any procedure specific to the study
* Patients who had at least one episode of smoking within the past 30 days before diagnosis

Exclusion Criteria

* History of another lung or head \& neck cancer \< 5 years (Note: The presence of a second tumour location, discovered at the same time as the lung or head and neck cancer, does not constitute a non-inclusion criterion)
* History of another cancer (except for curatively treated cervical cancer in situ and non-melanoma skin cancer) \< 3 years
* Mesothelioma, thymic malignancies, and cancer of the upper oesophagus
* Inability to complete the study for psychosocial reasons (inability to schedule interview (homeless), no access to phone, psychological disorder leading to inability to answer phone interview, do not speak French and no easy access to translator from surroundings)
* Patient under guardianship
* Patient refusal
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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International Agency for Research on Cancer

OTHER

Sponsor Role collaborator

Hospices Civils de Lyon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Hôpital Louis Pradel, Pneumologie

Bron, , France

Site Status

Hôpital de la Croix-Rousse, Oto-Rhino-Laryngologie et Chirurgie Cervico-Faciale

Lyon, , France

Site Status

Hôpital de la Croix-Rousse, Pneumologie

Lyon, , France

Site Status

Hôpital Lyon Sud, Pneumologie

Pierre-Bénite, , France

Site Status

Countries

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France

Other Identifiers

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69HCL22_0090

Identifier Type: -

Identifier Source: org_study_id

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