Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07102147

Increasing Adoption of a Telehealth-Delivered Collaborative Care Program for Patients With Lung Cancer: A Pilot Study

Led by Abramson Cancer Center at Penn Medicine · Updated on 2026-05-28

30

Participants Needed

1

Research Sites

13 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

Researchers are evaluating two different outreach methods, high touch versus standard outreach, to improve the use of a telehealth collaborative care program for patients with lung cancer who are experiencing depression and/or anxiety. This pilot study focuses on comparing how these outreach strategies affect patient engagement with the care program and aims to understand their impact on several related health and treatment outcomes. The study is led by the Abramson Cancer Center at Penn Medicine and explores the delivery of this care model via telehealth. Participants are randomly assigned to one of two groups. Those in the high touch outreach group receive multiple personalized contacts including gain-framed messages via text, email, portal messages, postal mail with a digital screener link, an informational flyer, and direct requests from their oncology providers if they do not respond. The standard outreach group receives a typical message similar to current practice through text, portal messages, email, or mail. The collaborative care program is adapted to be delivered remotely through telehealth. During the study, participants complete an intake assessment within 30 days after assignment and may attend oncology-based collaborative care appointments over the following months. Researchers measure the number of patients completing the intake and follow-up visits, track treatment retention up to 6 months, and assess changes in depression, anxiety, and fatigue symptoms using validated questionnaires. The study involves regular monitoring of symptom changes and treatment engagement to evaluate the effectiveness of the outreach strategies over time.

CONDITIONS

Brief Title

Telehealth Collaborative Care Model (CoCM) in Lung Cancer

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Are aged 18 years or older.
  • Are currently being seen by Penn Medicine Thoracic Oncology for lung cancer treatment or survivorship care.
  • Are referred to collaborative care by a Penn Medicine Thoracic Oncology clinician for treatment of depression, anxiety, or other psycho-therapy services.
Not Eligible

You will not qualify if you...

  • Are already receiving psycho-therapy treatment services outside of Penn Medicine's collaborative care program, Penn Integrated Care (PIC).
  • Have a significant and/or untreated medical and/or psychiatric co-morbidity (e.g., other cancers, schizophrenia, acute suicidal and/or homicidal ideation) that make them ineligible for the Penn CoCM program.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) for eligibility assessment

Treatment

Duration - Up to 6 months

Participants receive collaborative care via telehealth with either a high touch outreach strategy or standard outreach to support mental health treatment.

Multiple telehealth visits for collaborative care over treatment duration

Follow-up

Duration - Up to 6 months

Participants are assessed for treatment retention and clinical effectiveness using symptom questionnaires up to 6 months after treatment initiation.

Assessments conducted during and at end of treatment via telehealth

Trial Site Locations

Total: 1 location

1

Abramson Cancer Center at the University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104

Actively Recruiting

Loading map...

Research Team

J

Jennifer Steltz, MRA

J

Jocelyn Wainwright, MS

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

Similar Trials

Erectile Function After Percutaneous Coronary Intervention i...

Erectile Disfunction

Actively Recruiting

1 location

A Mobile-Delivered Personalized Feedback Intervention for Bl...

Alcohol Abuse

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

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