Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT05491213

TELESCOPE- TELEhealth Shared Decision-making COaching

Led by Rutgers, The State University of New Jersey · Updated on 2025-12-09

594

Participants Needed

2

Research Sites

206 weeks

Total Duration

On this page

Sponsors

R

Rutgers, The State University of New Jersey

Lead Sponsor

N

National Institutes of Health (NIH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Hypothesis 1a: The investigators anticipate that navigator decision coaching, compared to enhanced usual care (EUC) will result in higher quality SDM for lung cancer screening (LCS )(primary outcome), greater knowledge of lung cancer screening benefits and harms, and lower decisional conflict. Hypothesis 1b: Compared to enhanced usual care (EUC), we expect that TELESCOPE will result in more screening discussions, increased initial for lung cancer screening (LCS) with low-dose CT scan (LDCT) uptake among interested participants, increased adherence to repeat LCS and diagnostic testing, and increased smoking cessation referrals for current smokers. Hypothesis 2: The investigators expect that a "booster" coaching session will increase adherence to repeat lung cancer screening (LCS).

CONDITIONS

Official Title

TELESCOPE- TELEhealth Shared Decision-making COaching

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be between 50 and 77 years old
  • Be a current or former smoker who quit within the past 15 years
  • Have at least a 20 pack-year smoking history
  • Be scheduled for a non-acute care visit at a study site
  • Primary care clinicians, clinic directors, nursing directors, clinic practice administrators, or study navigators aged 18 or older and fluent in English may participate in interviews or surveys
Not Eligible

You will not qualify if you...

  • Do not speak English
  • Have a history of lung cancer
  • Were screened for lung cancer within the past 12 months
  • Have health conditions making curative treatment unlikely as determined by a primary care provider
  • Are unable to provide informed consent
  • Women who are pregnant

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 2 locations

1

Rutgers Cancer Institute

New Brunswick, New Jersey, United States, 08901

Actively Recruiting

2

The University of Texas MD Anderson Cancer Center

Houston, Texas, United States, 77030

Active, Not Recruiting

Loading map...

Research Team

J

Julie E Chapman-Greene, PhD, MPH

CONTACT

R

Rebecca Ayala

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SCREENING

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here