- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04635761
Awareness, Information, and Resources for Lung Cancer Screening Program for Community-Partnered Lung Cancer Screening
The Roswell AIR (Awareness, Information and Resources for Lung Cancer Screening) Program: A Community-Partnered Lung Cancer Screening Intervention
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
PRIMARY OBJECTIVES:
I. Collaborate with community organizations and leaders to leverage community-based assets to disseminate education about lung cancer screening.
II. Reach medically underserved, high risk community members. III. Enhance lung cancer screening knowledge among medically underserved, high risk community members.
IV. Navigate screening-eligible community members to lung cancer screening.
OUTLINE:
Participants complete the Roswell Awareness, Information and Resources for Lung Cancer Screening (AIR) Program over 45 minutes and then receive the High-Risk Lung Cancer Tip Sheet.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New York
-
Buffalo, New York, United States, 14263
- Roswell Park Cancer Institute
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Members of all races and ethnic groups are eligible for this study
Exclusion Criteria:
- Adults unable to consent
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Prevention (AIR Program)
Participants complete the Roswell Awareness, Information and Resources for Lung Cancer Screening (AIR) Program over 45 minutes and then receive the High-Risk Lung Cancer Tip Sheet..
|
Complete AIR Program and receive the High-Risk Lung Cancer Tip Sheet
Other Names:
Ancillary studies
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of programs offered
Time Frame: Up to 1 year
|
Up to 1 year
|
|
|
Average number of attendees at each site
Time Frame: Up to 1 year
|
Up to 1 year
|
|
|
Demographics of attendees at each site
Time Frame: Up to 1 year
|
Up to 1 year
|
|
|
Number of medically underserved, high risk community members reached
Time Frame: Up to 1 year
|
Up to 1 year
|
|
|
Percent change in lung cancer screening awareness as assessed before and after program completion
Time Frame: Up to 1 year
|
Pre and post questionnaire to be given to participants
|
Up to 1 year
|
|
Percent change in knowledge of eligibility guidelines for screening as assessed before and after program completion
Time Frame: Up to 1 year
|
Pre and post questionnaire to be given to participants before and after educational sessions
|
Up to 1 year
|
|
Percent Change in knowledge of benefits of early detection as assessed before and after program completion
Time Frame: Up to 1 year
|
Pre and post questionnaire to be completed by participants before and after educational sessions
|
Up to 1 year
|
|
Change in fear, worry, and increased health-related self-efficacy
Time Frame: Up to 1 year
|
Pre and post questionnaire to be completed by participants before and after educational sessions
|
Up to 1 year
|
|
Number of screening eligible individuals reached
Time Frame: Up to 1 year
|
Up to 1 year
|
|
|
Number of screening eligible individuals navigated to lung cancer screening
Time Frame: Up to 1 year
|
Up to 1 year
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Elizabeth Bouchard, Roswell Park Cancer Institute
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- I 781020 (Other Identifier: Roswell Park Cancer Institute)
- NCI-2020-08297 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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