Breast Cancer Clinical Trial

Video-Based Intervention in Reducing Anxiety in Patients Undergoing Lung Cancer Screening

Summary

This pilot trial studies a video-based intervention in reducing anxiety in patients undergoing lung cancer screening. Giving a video-based intervention to patients prior to lung cancer screening may reduce anxiety and improve the well-being and quality of life.

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Full Description

PRIMARY OBJECTIVES:

I. Test the feasibility and acceptability of the video-based intervention.

SECONDARY OBJECTIVES:

I. To describe incidence, degree, and duration of screen-related anxiety among individuals scheduled to undergo low-dose computed tomography (CT) scan (LDCT) for lung cancer screening (LCS).

II. To describe baseline patient characteristics and pre-screening anxiety levels.

III. To describe the preliminary outcomes on screen-related anxiety for patients both not in the intervention group and those in the intervention group.

OUTLINE: Patients are assigned to 1 of 2 groups.

GROUP I: Patients receive standard of care following LCS consisting of routine visits and telephone contact with the LCS program nurse practitioner and coordinator.

GROUP II: Patients undergo a video-based intervention prior to undergoing LCS. Patients watch a 5-minute video that focuses on preparing patients for LCS by providing information on the following: program team and contact information; reason to be screened; screening eligibility; how screening is performed; what to expect on the day of screening; what to expect after screening; what to expect if result is positive; what to expect if result is negative; and risks of screening. Patients also receive an educational handbook. Patients with positive scans (a Lung-Imaging Reporting and Data Systems [RADS] 3 or 4) receive additional brochure and nursing support within 1 week after notification of scan results.

After completion of LCS, patients are followed up at 1 week and then at 3 and 7 months.

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Eligibility Criteria

Inclusion Criteria:

This study will be conducted in people scheduled to undergo baseline LDCT as part of the City of Hope (COH) LCS program
There are no restrictions related to performance status and life expectancy
All subjects must have the ability to understand and the willingness to participate in the informed consent process, although a waiver of written informed consent is obtained for this study

Exclusion Criteria:

Patients who do not speak or read, because all intervention materials, including the video and written materials are in English
Subjects, who in the opinion of the investigator, may not be able to comply with study procedures

Study is for people with:

Breast Cancer

Estimated Enrollment:

20

Study ID:

NCT02288416

Recruitment Status:

Completed

Sponsor:

City of Hope Medical Center

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There is 1 Location for this study

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City of Hope Medical Center
Duarte California, 91010, United States

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Study is for people with:

Breast Cancer

Estimated Enrollment:

20

Study ID:

NCT02288416

Recruitment Status:

Completed

Sponsor:


City of Hope Medical Center

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