Study Results
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View full resultsBasic Information
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Recruitment Status
COMPLETED
Clinical Phase
NA
Total Enrollment
512 participants
Study Classification
INTERVENTIONAL
Study Start Date
2023-08-02
Study Completion Date
2024-07-30
Brief Summary
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LungTalk and leveraging Facebook-targeted Advertisement (FBTA) addresses the call to develop and test multi-level, cancer communication interventions using innovative methods and designs. The study's long term goal is to increase lung cancer screening uptake among appropriate, high-risk individuals nationwide.
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Detailed Description
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Conditions
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Lung Cancer
Study Design
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Allocation Method
RANDOMIZED
Intervention Model
PARALLEL
Primary Study Purpose
SCREENING
Blinding Strategy
NONE
Study Groups
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Tailored health communication intervention (LungTalk)
Participants will receive the tailored health intervention "LungTalk". LungTalk is a 10-15 minute long computer-tailored health communication and decision-making tool that is theoretically grounded in the Conceptual Model on Lung Cancer Screening Participation.
Group Type
EXPERIMENTAL
LungTalk
Intervention Type
BEHAVIORAL
LungTalk is a 10-15 minute long computer-tailored health communication and decision-making tool.
Non-tailored Intervention
Participants will receive non-tailored American Cancer Society (ACS) Lung Screening Informational Video as per standard of care. ACS Lung Screening Informational Video (ACS LSIV) is a non-tailored 5-minute video from the American Cancer Society about lung cancer screening designed for the lay individual.
Group Type
ACTIVE_COMPARATOR
Non-tailored intervention - Standard of practice
Intervention Type
BEHAVIORAL
ACS Lung Screening Informational Video
Interventions
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LungTalk
LungTalk is a 10-15 minute long computer-tailored health communication and decision-making tool.
Intervention Type
BEHAVIORAL
Non-tailored intervention - Standard of practice
ACS Lung Screening Informational Video
Intervention Type
BEHAVIORAL
Eligibility Criteria
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Inclusion Criteria
* ≥20-pack-year smoking history;
* Individuals who currently smoke or quit smoking within the past 15 years
* Individuals who currently smoke or quit smoking within the past 15 years
Exclusion Criteria
* Previously undergone LDCT for early detection of lung cancer, have a lung nodule or nodules that are currently being followed
* Has ever been diagnosed with lung cancer
* Individuals with impaired decision-making (because our primary outcome is decision-making, we will not include individuals with impaired decision-making)
* Has ever been diagnosed with lung cancer
* Individuals with impaired decision-making (because our primary outcome is decision-making, we will not include individuals with impaired decision-making)
Minimum Eligible Age
50 Years
Maximum Eligible Age
80 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
Yes
Sponsors
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National Cancer Institute (NCI)
NIH
Sponsor Role
collaborator
Hackensack Meridian Health
OTHER
Sponsor Role
lead
Responsible Party
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Responsibility Role
SPONSOR
Principal Investigators
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Lisa Carter-Bawa, PhD
Role: PRINCIPAL_INVESTIGATOR
Hackensack Meridian Health
Locations
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Hackensack Meridian Health - Center for Discovery and Innovation
Nutley, New Jersey, United States
Site Status
Countries
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United States
References
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Carter-Bawa L, Banerjee SC, Comer RS, Kale MS, King JC, Leopold KT, Monahan PO, Ostroff JS, Slaven JE Jr, Valenzona F, Wiener RS, Rawl SM. Leveraging social media to increase lung cancer screening awareness, knowledge and uptake among high-risk populations (The INSPIRE-Lung Study): study protocol of design and methods of a community-based randomized controlled trial. BMC Public Health. 2023 May 26;23(1):975. doi: 10.1186/s12889-023-15857-8.
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Lisa CB, Banerjee SC, Ostroff JS, Kale MS, King JC, Leopold KT, Monahan PO, Slaven JE Jr, Wiener RS, Valenzona F, Rawl SM, Comer RS. Leveraging social media to increase lung cancer screening awareness, knowledge and uptake among high-risk populations (The INSPIRE-Lung Study): Study protocol of design and methods of a community-based randomized controlled trial. Res Sq [Preprint]. 2023 May 4:rs.3.rs-2846041. doi: 10.21203/rs.3.rs-2846041/v1.
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DERIVED
Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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Pro2022-0860
Identifier Type: -
Identifier Source: org_study_id
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