Clinical Trials Directory

Trials / Completed

CompletedNCT02288416

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

Pilot Study of a Video-Based Intervention to Reduce Psychological Harm Associated With Lung Cancer Screening

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
City of Hope Medical Center · Academic / Other
Sex
All
Age
55 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
OTHEReducational interventionUndergo video-based intervention
OTHERquestionnaire administrationAncillary studies
OTHERquality-of-life assessmentAncillary studies
OTHERBest Practice

Timeline

Start date
2014-12-08
Primary completion
2018-09-06
Completion
2018-09-06
First posted
2014-11-11
Last updated
2018-09-10

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02288416. Inclusion in this directory is not an endorsement.