Esophageal Cancer Clinical Trial
Official title:
Evaluation of the Implementation of an Early Integrated Palliative Care Program in the Esophageal Cancer Population
Palliative care physicians and nurses are trained to help reduce suffering and improve
quality of life in patients under their care. Their services also include other components
such as referral to dietitians, social workers and community resources, to assist patients in
their homes. In addition to this, they may also administer interventions to make patients
more comfortable, assisting them and their families in making important decisions and
providing support, during that time.
At present, palliative care is provided to esophageal cancer patients on an as-needed basis,
through the referral of a heath care professional or the patient's request. This study aims
to assess the impact of the integration of early palliative care combined with appropriate
medical care in the metastatic esophageal cancer population, so that patients can benefit
from these services at an earlier stage. It is hoped that this will improve quality of life,
symptom management, depression and anxiety, as well as survival.
Previous reports suggest that starting palliative care early in patients with breast,
colorectal, prostate and lung cancers appear to improve quality of life, symptom management,
depression, anxiety and perhaps even survival, but it has never been tested in patients with
esophageal cancer.This study aims to assess the impact of the introduction of early
palliative care services on the esophageal cancer population, as opposed to traditional
palliative care, which is provided on an as-needed basis, usually in end-of-life situations.
The study is a prospective one-armed pre-post intervention evaluation. Eligible patients that
have consented will receive an early consultation with the palliative care group. In addition
to this, the patients will be administered appropriate oncological care including surgical,
brachytherapy, chemotherapy or radiotherapy services. The patients will be referred to the
palliative service at the time of consent, with a consultation taking place within one week
of referral receipt. The nurses and physicians involved in the palliative service will not
only provide symptom management, psychosocial support, assistance with treatment related
decisions and other patient needs. Information about symptoms, anxiety and depression, and
quality of life will be collected through surveys at two timepoints - at baseline, when the
patient consents and at 12 weeks post diagnosis of metastatic disease. The primary outcome of
the study is the change in quality of life perceived by esophageal cancer patients at the two
timepoints. Secondary outcomes include differences in esophageal cancer specific symptoms and
anxiety and depression scores at the two timepoints, as well as patient survival information.
This study is integrated into the currently operational Esophageal Diagnostic Assessment
Program (EDAP) conceptualized and implemented at St. Joseph's Healthcare Hamilton. It is
hoped that this study will also help to establish the full integration of palliative care
into the overall care of patients with esophageal cancer.
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