Awareness, Information, and Resources for Lung Cancer Screening Program for Community-Partnered Lung Cancer Screening

September 27, 2022 updated by: Roswell Park Cancer Institute

The Roswell AIR (Awareness, Information and Resources for Lung Cancer Screening) Program: A Community-Partnered Lung Cancer Screening Intervention

This trial investigates an educational program called Awareness, Information, and Resources for Lung Cancer Screening Program in improving knowledge about lung cancer screening in medically underserved communities. This program aims to educate and remove barriers to lung cancer screening among medically underserved community members who are eligible for lung cancer screening, and to improve access to evidence-based screening guidelines for early detection for lung cancer in the Western New York area.

Study Overview

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

Interventional

Enrollment (Actual)

292

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • New York
      • Buffalo, New York, United States, 14263
        • Roswell Park Cancer Institute

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Members of all races and ethnic groups are eligible for this study

Exclusion Criteria:

  • Adults unable to consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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:
  • Education for Intervention
  • Intervention by Education
  • Intervention through Education
  • Intervention, Educational
Ancillary studies

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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Elizabeth Bouchard, Roswell Park Cancer Institute

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 30, 2020

Primary Completion (Actual)

August 25, 2021

Study Completion (Actual)

August 25, 2022

Study Registration Dates

First Submitted

November 5, 2020

First Submitted That Met QC Criteria

November 13, 2020

First Posted (Actual)

November 19, 2020

Study Record Updates

Last Update Posted (Actual)

September 28, 2022

Last Update Submitted That Met QC Criteria

September 27, 2022

Last Verified

September 1, 2022

More Information

Terms related to this study

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

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

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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