Actively Recruiting

Phase Not Applicable
Age: 50Years - 80Years
All Genders
NCT06638554

Integrating Telehealth to Advance Lung Cancer Screening

Led by Abramson Cancer Center at Penn Medicine · Updated on 2025-11-12

6000

Participants Needed

1

Research Sites

133 weeks

Total Duration

On this page

Sponsors

A

Abramson Cancer Center at Penn Medicine

Lead Sponsor

N

National Institutes of Health (NIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this pragmatic trial is to learn if telehealth strategies can increase shared decision-making (SDM) for lung cancer screening (LCS). It will also learn about the equity of these strategies by conducting non-inferiority analysis by race and sex. The main questions it aims to answer are: 1. Does patient outreach using synchronous and asynchronous telehealth strategies increase completion of SDM visits for LCS? 2. Is the effectiveness of these telehealth strategies similar by race and sex? The study uses a Sequential Multiple Assignment Randomized Trial (SMART) design and includes two stages of interventions. The first stage of intervention includes direct patient outreach with an invitation to schedule either a 1) telehealth SDM visit or 2) telehealth or in-person SDM visit. Participants that do not respond to the first stage interventions receive a text message reminder encouraging SDM visit completion with or without digital care coordination.

CONDITIONS

Official Title

Integrating Telehealth to Advance Lung Cancer Screening

Who Can Participate

Age: 50Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 50 to 80 years
  • Have a documented history of 20 pack-year or greater smoking or self-reported smoking history
  • Currently smoke or formerly smoked cigarettes
  • No documented history of lung cancer
  • No lung cancer screening in the 24 months before enrollment
  • Completed at least one primary care visit at Penn Medicine in the last 3 years
Not Eligible

You will not qualify if you...

  • Does not meet all inclusion criteria

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Trial Site Locations

Total: 1 location

1

University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

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Research Team

K

Katharine Rendle, PhD

CONTACT

H

Hannah Toneff, MSW, MA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

4

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