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Palliative Care Interventions for Outpatients Newly Diagnosed With Lung Cancer: Phase II — PCI2  

Lung Cancer Clinical Trial

Official title:
Palliative Care Interventions for Outpatients Newly Diagnosed With Lung Cancer: Phase II

Clinical Trial Summary

The focus of the study is to test a nurse-led telephone-based palliative care intervention on improving the delivery of care for patients with newly diagnosed lung cancer. The study is a three site randomized control trial to determine the efficacy of the intervention on improving patients' quality of life, symptom burden, and satisfaction of care. Additionally, the study will test an innovative care delivery model to improve patients' access to palliative care. The investigators will also determine the effect of the intervention on patient activation to discuss treatment preferences with their clinician and on clinician knowledge of patients' goals of care.

Clinical Trial Description

Patients meeting entry criteria will be randomized to the intervention arm, palliative care plus usual care, or the usual care arm. Patients randomized to the intervention arm will receive usual oncologic care and phone calls from a nurse. Outcome measures will be collected at baseline and at the end of the patients' primary cancer treatment. The study will be performed at the Puget Sound Health Care System, Birmingham VA and Portland VA. The investigators will recruit individuals (n=138) with lung cancer over 2.5 years. The primary objective is to determine the efficacy of the nurse-led telephone-based palliative intervention on improving patients' quality of life, symptom burden, and satisfaction of care. In addition, using validated instruments, the investigators will assess the effect of the intervention on patient activation to discuss treatment preferences with their clinician and on clinician knowledge of patients' goals of care. The results of this study will inform a future effectiveness/implementation study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03007953
Study type Interventional
Source VA Office of Research and Development
Contact
Status Completed
Phase N/A
Start date December 5, 2016
Completion date December 11, 2019
View Details
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