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

Study 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.

Ask AI to explain this study

Start here

Key things to know

Main goalSupportive Care

This describes the study’s primary purpose.

What is being studiededucational intervention and questionnaire administration

Plus 2 other study approaches.

Who it may be forAnxiety · No Evidence of Disease

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Sep 10, 2018 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Interventional

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?City of Hope Medical Center

Study sponsor

Study overview

What this study is about

Purpose: Supportive Care
Study type: Interventional
Phase: Not applicable
Sponsor: City of Hope Medical Center
Interventions being studied: Other: educational intervention; Other: questionnaire administration; Other: quality-of-life assessment; Other: Best Practice

Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

Study topics

Survivorship and quality of life→

Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion 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

Reasons someone may not be able to joinExclusion 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

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

Study sites

U.S. locations

City of Hope Medical CenterDuarte, California

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Sep 10, 2018. Always confirm current availability with the study team.

View original record ↗