Evaluating a Bidirectional Priming Intervention for Goals-of-care Communication in Oncology

Completed · Not applicable

Conditions studied: Lung Cancers, Gastrointestinal Cancers

In brief

This pilot study will evaluate whether an intervention aimed at hospitalized patients with advanced lung and gastrointestinal cancers can help facilitate goals-of-care (GOC) communication with their oncologists after discharge. While GOC communication is a recommended component of routine oncology care, many patients with solid cancers do not have the opportunity to talk with their oncologist about their goals and end-of-life preferences. Prior research has shown that a systematic method of prompting GOC communication with at-risk patients would address a key barrier to timely GOC communication and ensure that patients receive care that is in line with their personal preferences. This trial will enroll 80 participants, who will be randomized 1:1 to either an intervention or a control group. Participants in the intervention group will complete a short survey regarding their goals, preferences, and disease understanding. Survey responses will be shared with each participant's outpatient oncology team. Oncologists will subsequently receive a nudge in the electronic medical record reminding them of key survey responses and encouraging them to discuss them at the patient's first clinic visit after hospital discharge. The primary feasibility outcome is intervention completion rate and the primary clinical outcome is GOC documentation within 30 days of discharge in the intervention group compared to the control group.

Key facts

Study ID

NCT06955468

Run by

Abramson Cancer Center at Penn Medicine

People needed

40

Starts

2025-07-21

Expected to finish

2026-03-01

Last updated by the study team

2026-03-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Unplanned admission to the HUP Solid Oncology service;
• Underlying diagnosis of advanced lung or GI cancer, defined as metastatic or locally advanced disease;
• Anticipated discharge within the next 72h; and
• Primary oncologist is based at HUP; or
• Family member/caregiver of a patient meeting the above 4 criteria.

You may not qualify if…

• Unable to complete survey in English.

Where it is running

• Hospital of the University of Pennsylvania — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.