Lung Cancer Screening Eligibility Assessment

Sponsor
Abramson Cancer Center at Penn Medicine (Other)
Overall Status
Recruiting
CT.gov ID
NCT06133816
Collaborator
National Institutes of Health (NIH) (NIH), National Cancer Institute (NCI) (NIH)
6,000
1
12
7
861.4

Study Details

Study Description

Brief Summary

The primary purpose of this study evaluate if different messaging impacts response rates to a brief survey (i.e., the simplified eligibility tool) that is designed to estimate pack-year eligibility for lung cancer screening (LCS). This will help inform the best way to increase response rates to the tool in future intervention studies designed to increase LCS, and expand upon survey methodology in general.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Framed Introductory Message A
  • Behavioral: Framed Introductory Message B
  • Behavioral: Framed Introductory Message C
  • Behavioral: Framed Tobacco Use Message A
  • Behavioral: Framed Tobacco Use Message B
  • Behavioral: Financial Incentive
N/A

Detailed Description

Despite growing evidence that lung cancer screening (LCS) reduces lung cancer-specific mortality, LCS across the United States is remarkably low. This is due in part to challenges with identifying adults who meet eligibility criteria for lifetime smoking intensity (i.e., 20 pack-years or greater), which is often missing from the electronic medical record. We have developed a simplified eligibility tool that has shown accuracy in estimating pack-years. But given the potential for low response rates, there is a great need to identify effective strategies to increasing response rates equitably prior to using it in practice or in future studies. The primary purpose of this study evaluate if different messaging impacts response rates to a brief survey (i.e., the simplified eligibility tool) that is designed to estimate pack-year eligibility for lung cancer screening (LCS). This will help to identify the best way to increase response rates to the tool in future intervention studies designed to increase LCS, and expand upon survey methodology in general.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
6000 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Intervention Model Description:
We will use a randomized factorial design to test the effects of different types of messaging with or without incentives on response rates to an eligibility survey.We will use a randomized factorial design to test the effects of different types of messaging with or without incentives on response rates to an eligibility survey.
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Health Services Research
Official Title:
Using a Simplified Tool to Predict Lung Cancer Screening (LCS) Eligibility: Experiment to Test Effects of Messaging on Response Rates
Actual Study Start Date :
Jul 31, 2023
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Feb 28, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Arm 1 (Introductory Message A + Tobacco Use Message A + Incentive)

Participants will receive two framed messages (AA) plus an incentive

Behavioral: Framed Introductory Message A
Randomly assign patients to receive introductory message encouraging them to complete the survey (version A).

Behavioral: Framed Tobacco Use Message A
Randomly assign patients to receive norming message related to tobacco use (version A).

Behavioral: Financial Incentive
Randomly assigned patients to be entered into a drawing to receive a $100 gift card.

Experimental: Arm 2 (Introductory Message A + Tobacco Use Message A)

Participants will receive two framed messages (AA)

Behavioral: Framed Introductory Message A
Randomly assign patients to receive introductory message encouraging them to complete the survey (version A).

Behavioral: Framed Tobacco Use Message A
Randomly assign patients to receive norming message related to tobacco use (version A).

Experimental: Arm 3 (Introductory Message A + Tobacco Use Message B + Incentive)

Participants will receive two framed messages (AB) plus an incentive

Behavioral: Framed Introductory Message A
Randomly assign patients to receive introductory message encouraging them to complete the survey (version A).

Behavioral: Framed Tobacco Use Message B
Randomly assign patients to receive norming message related to tobacco use (version B).

Behavioral: Financial Incentive
Randomly assigned patients to be entered into a drawing to receive a $100 gift card.

Experimental: Arm 4 (Introductory Message A + Tobacco Use Message B)

Participants will receive two framed messages (AB)

Behavioral: Framed Introductory Message A
Randomly assign patients to receive introductory message encouraging them to complete the survey (version A).

Behavioral: Framed Tobacco Use Message B
Randomly assign patients to receive norming message related to tobacco use (version B).

Experimental: Arm 5 (Introductory Message B + Tobacco Use Message A + Incentive)

Participants will receive two framed messages (BA) plus an incentive

Behavioral: Framed Introductory Message B
Randomly assign patients to receive introductory message encouraging them to complete the survey (version B).

Behavioral: Framed Tobacco Use Message A
Randomly assign patients to receive norming message related to tobacco use (version A).

Behavioral: Financial Incentive
Randomly assigned patients to be entered into a drawing to receive a $100 gift card.

Experimental: Arm 6 (Introductory Message B + Tobacco Use Message A)

Participants will receive two framed messages (BA)

Behavioral: Framed Introductory Message B
Randomly assign patients to receive introductory message encouraging them to complete the survey (version B).

Behavioral: Framed Tobacco Use Message A
Randomly assign patients to receive norming message related to tobacco use (version A).

Experimental: Arm 7 (Introductory Message B + Tobacco Use Message B + Incentive)

Participants will receive two framed messages (BB) plus an incentive

Behavioral: Framed Introductory Message B
Randomly assign patients to receive introductory message encouraging them to complete the survey (version B).

Behavioral: Framed Tobacco Use Message B
Randomly assign patients to receive norming message related to tobacco use (version B).

Behavioral: Financial Incentive
Randomly assigned patients to be entered into a drawing to receive a $100 gift card.

Experimental: Arm 8 (Introductory Message B + Tobacco Use Message B)

Participants will receive two framed messages (BB)

Behavioral: Framed Introductory Message B
Randomly assign patients to receive introductory message encouraging them to complete the survey (version B).

Behavioral: Framed Tobacco Use Message B
Randomly assign patients to receive norming message related to tobacco use (version B).

Experimental: Arm 9 (Introductory Message C + Tobacco Use Message A + Incentive)

Participants will receive two framed messages (CA) plus an incentive

Behavioral: Framed Introductory Message C
Randomly assign patients to receive introductory message encouraging them to complete the survey (version C).

Behavioral: Framed Tobacco Use Message A
Randomly assign patients to receive norming message related to tobacco use (version A).

Behavioral: Financial Incentive
Randomly assigned patients to be entered into a drawing to receive a $100 gift card.

Experimental: Arm 10 (Introductory Message C + Tobacco Use Message A)

Participants will receive two framed message (CA)

Behavioral: Framed Introductory Message C
Randomly assign patients to receive introductory message encouraging them to complete the survey (version C).

Behavioral: Framed Tobacco Use Message A
Randomly assign patients to receive norming message related to tobacco use (version A).

Experimental: Arm 11 (Introductory Message C + Tobacco Use Message B + Incentive)

Participants will receive two framed messages (CB) plus an incentive

Behavioral: Framed Introductory Message C
Randomly assign patients to receive introductory message encouraging them to complete the survey (version C).

Behavioral: Framed Tobacco Use Message B
Randomly assign patients to receive norming message related to tobacco use (version B).

Behavioral: Financial Incentive
Randomly assigned patients to be entered into a drawing to receive a $100 gift card.

Experimental: Arm 12 (Introductory Message C + Tobacco Use Message B)

Participants will receive two framed messages (CB)

Behavioral: Framed Introductory Message C
Randomly assign patients to receive introductory message encouraging them to complete the survey (version C).

Behavioral: Framed Tobacco Use Message B
Randomly assign patients to receive norming message related to tobacco use (version B).

Outcome Measures

Primary Outcome Measures

  1. Full Survey Completion [7 days]

    The proportion of participants that answers all three survey questions via text message among all those randomized.

Secondary Outcome Measures

  1. Partial Survey Completion [7 days]

    The proportion of participants that answer at least one of three survey questions via text message among all those randomized.

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. meet age eligibility (50-80 years old) for LCS based on 2021 USPSTF guidelines; and

  2. have completed at least one primary care visit at Penn Medicine in 2020-2025

Exclusion Criteria:
  1. have a documented history of lung cancer;

  2. have a documented history of completing LCS at Penn Medicine;

  3. are listed as not wanting to be contacted or solicited for research; or

  4. do not otherwise meet inclusion criteria.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Pennsylvania Philadelphia Pennsylvania United States 19104

Sponsors and Collaborators

  • Abramson Cancer Center at Penn Medicine
  • National Institutes of Health (NIH)
  • National Cancer Institute (NCI)

Investigators

  • Principal Investigator: Katharine A Rendle, PhD,MSW,MPH, University of Pennsylvania

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
Katharine Rendle, Assistant Professor, Abramson Cancer Center at Penn Medicine
ClinicalTrials.gov Identifier:
NCT06133816
Other Study ID Numbers:
  • 850376
  • P50CA271338-02
First Posted:
Nov 18, 2023
Last Update Posted:
Nov 29, 2023
Last Verified:
Nov 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Katharine Rendle, Assistant Professor, Abramson Cancer Center at Penn Medicine
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 29, 2023