Development and Feasibility Testing of a Lung Cancer Screening Decision Aid

NCT ID: NCT02790866

Last Updated: 2019-04-03

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

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-03-31

Study Completion Date

2016-12-31

Brief Summary

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This study evaluates the feasibility and acceptability of LuCaS Choices, a web-based decision aid designed to facilitate informed decision making about participation in lung cancer screening among individuals at high risk of lung cancer due to heavy cigarette smoking.

Detailed Description

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The proposed project will develop an innovative web-based decision aid (DA) to improve decision making for lung cancer screening (LCS) among individuals at high risk for lung cancer due to cigarette smoking. Recent National Lung Screening Trial (NLST) data demonstrated a 20% relative reduction in lung cancer mortality for low dose computed tomography screening as compared to chest X-ray among individuals at high lung cancer risk. Given that lung cancer is the leading cause of cancer death in the United States with an estimated 160,340 deaths predicted for 2012, the new data have reinvigorated interest in LCS. However, LCS carries substantial risks including a high false positive rate, over-diagnosis, adverse psychosocial consequences, and increased radiation exposure. Further, it is unknown whether LCS would reduce lung cancer mortality among individuals who smoke but do not meet NLST eligibility criteria. Therefore, there is currently no clear best choice for whether a given individual should be screened or not. Decisions about participating in LCS should be well informed and consistent with individual preferences. However, previous data indicate that individuals who do undergo LCS rarely have a thorough understanding of the risks or benefits.

To address this rapidly emerging public health challenge, this research has developed a web-based decision aid (DA) to facilitate informed decision making regarding LCS in individuals at high risk for lung cancer (i.e., cigarette smokers), and will assess feasibility of DA administration and proposed methods for conducting a future randomized clinical trial (RCT) of DA effectiveness. The content of the DA will be based on the investigators previous studies exploring LCS decision making and other recent research.

The specific aim of the currently proposed research are to conduct a feasibility trial of the DA among individuals at high risk of lung cancer due to heavy cigarette smoking. Investigators will recruit participants to assess feasibility of: 1) delivering the DA intervention in a community setting, and 2) conducting research procedures and assessment tools as planned for a future RCT.

Conditions

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Lung Neoplasms

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SCREENING

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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LuCaS Decision Aid

Access to LuCaS, a web-based lung cancer screening decision aid

Group Type EXPERIMENTAL

LuCaS Decision Aid

Intervention Type BEHAVIORAL

Web-based Lung Cancer Screening Decision Aid

NCI Website

Access to NCI website on lung cancer screening

Group Type ACTIVE_COMPARATOR

NCI Website

Intervention Type BEHAVIORAL

NCI Website on Lung Cancer Screening

Interventions

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LuCaS Decision Aid

Web-based Lung Cancer Screening Decision Aid

Intervention Type BEHAVIORAL

NCI Website

NCI Website on Lung Cancer Screening

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* be at least 40 years of age
* history of 20 or more pack years of smoking
* ability to read and understand English
* must have a personal phone
* must have Internet access

Exclusion Criteria

* reporting or demonstrating significant psychological distress
Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Miami

OTHER

Sponsor Role collaborator

Jamie Studts

OTHER

Sponsor Role lead

Responsible Party

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Jamie Studts

Associate Professor

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Jamie L Studts, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Kentucky

Margaret M Byrne, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Miami

Locations

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University of Miami (FL)

Miami, Florida, United States

Site Status

University of Kentucky

Lexington, Kentucky, United States

Site Status

Countries

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United States

Other Identifiers

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15-0001-P1H

Identifier Type: -

Identifier Source: org_study_id

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