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NCT06955468 | NOT YET RECRUITING | Lung Cancers

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

Abramson Cancer Center at Penn Medicine

Brief Summary:

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.

Condition or disease

Lung Cancers

Gastrointestinal Cancers

Intervention/treatment

Priming Survey

Phase

NA

Study Type : INTERVENTIONAL
Estimated Enrollment : 80 participants
Masking : NONE
Primary Purpose : SUPPORTIVE_CARE
Official Title : Development of a Bidirectional Priming Intervention for Goals-of-care Communication in Oncology
Actual Study Start Date : 2025-07
Estimated Primary Completion Date : 2026-01
Estimated Study Completion Date : 2026-05

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • 1. Unplanned admission to the HUP Solid Oncology service;
  • 2. Underlying diagnosis of advanced lung or GI cancer, defined as metastatic or locally advanced disease;
  • 3. Anticipated discharge within the next 72h; and
  • 4. Primary oncologist is based at HUP; or
  • 5. Family member/caregiver of a patient meeting the above 4 criteria.
Exclusion Criteria
  • 1. Unable to complete survey in English.
Evaluating a Bidirectional Priming Intervention for Goals-of-care Communication in Oncology

Location Details

NCT06955468

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How to Participate

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Locations

Not yet recruiting

United States, Pennsylvania

Hospital of the University of Pennsylvania

Philadelphia, Pennsylvania, United States, 19104