Lung Cancer Clinical Trial

Pre-Post Study for Supporting Appropriate Implementation of Lung Cancer Screening

Summary

The primary objective of this study is to assess the effect of the decision aid on measures of decision-making such as knowledge, screening attitudes, decisional conflict, and screening intent.

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Full Description

Using a single group, pre-post design, we aim to assess the effect of the decision aid on screening knowledge, screening attitudes, decisional conflict, and screening intent within 3 months of decision aid viewing.

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Eligibility Criteria

Inclusion Criteria:

Subjects must meet all of the following inclusion criteria to participate in this study:

Age 55 - 80;
Current smoker, or former smoker who has less than a 16-year quit history;
Have at least a 30-pack year smoking history (average packs per day * years smoking); and
Patient of the Internal Medicine Clinic at University of North Carolina Health Care.

Exclusion Criteria:

All subjects meeting any of the following exclusion criteria at baseline will be excluded from study participation:

Ever diagnosed with lung cancer;
Undergone chemotherapy or radiation therapy in the past 18 months prior to enrollment;
Coughed up blood from lungs (also called hemoptysis) within the past year prior to enrollment;
Experienced unexplained weight loss of 15-pounds or more during six months prior to enrollment; and
Had a chest CT scan within the past 18 months prior to enrollment.

Study is for people with:

Lung Cancer

Estimated Enrollment:

62

Study ID:

NCT03077230

Recruitment Status:

Completed

Sponsor:

UNC Lineberger Comprehensive Cancer Center

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There is 1 Location for this study

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UNC Ambulatory Care Center Internal Medicine Clinic
Chapel Hill North Carolina, 27599, United States

How clear is this clinincal trial information?

Study is for people with:

Lung Cancer

Estimated Enrollment:

62

Study ID:

NCT03077230

Recruitment Status:

Completed

Sponsor:


UNC Lineberger Comprehensive Cancer Center

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