This pilot clinical trial studies a palliative care program in improving the quality of life of patients with newly diagnosed pancreatic cancer. Palliative care is care given to patients who have a serious or life-threatening disease, and focuses on managing disease symptoms, side effects of treatment or the disease, and improving patient quality of life. Studying a palliative care program used for other types of cancer may help doctors learn whether it can improve the quality of life of patients with pancreatic cancer.
PRIMARY OBJECTIVES: I. To pilot-test an interdisciplinary Palliative Care Planning Intervention (PCPI) in pancreatic cancer. Specifically, to describe patients' satisfaction with the timing, content, and delivery of the PCPI intervention. SECONDARY OBJECTIVES: I. To pilot-test all selected measures for the study, including measures for healthcare resource utilization, overall cost, and patient/family out of pocket expenses. II. The long-term objective of this pilot study is to conduct a larger PCPI intervention study for pancreatic cancer patients and evaluate its impact on quality of life (QOL), symptom intensity, healthcare resource utilization, and healthcare costs. OUTLINE: Patients receive a handbook titled "Supporting You During Cancer Treatment" with educational material on QOL issues. Patients undergo 2 education sessions on handbook material in-person or by telephone, with session 1 focusing on physical and social well-being issues and session 2 focusing on psychological and spiritual well-being issues. At the beginning of each session, patients select 3 priority topics from a list, and content is tailored to patient needs. After completion of study, patients are followed up at 1 and 2 months.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
10
Undergo PCPI
Undergo PCPI
Undergo QOL assessment
Undergo questionnaire administration
City of Hope Medical Center
Duarte, California, United States
Reasons for refusal to participate
Descriptive statistics will be provided.
Time frame: Up to 2 months
Reasons for failure to complete study
Descriptive statistics will be provided.
Time frame: Up to 2 months
Attendance at two educational sessions
Descriptive statistics will be provided.
Time frame: Up to 2 months
Completion of intervention
Descriptive statistics will be provided.
Time frame: Up to 2 months
Patient satisfaction with timing, content, and delivery of PCPI
Presented through summary statistics of data from the patient satisfaction tool.
Time frame: Up to 2 months
Qualitative interview data
Each interview transcript will be initially reviewed to provide a glimpse of potential domains and targets. Content analysis will be conducted on the transcribed qualitative data. Transcripts will be assigned codes. Content analysis occurring through coding consisting of line-by-line analysis with themes identified will be initiated. The research team will independently analyze selected segments of the data to verify themes. Coding will be checked and validated by the principal investigator and research team.
Time frame: Up to 2 months
Healthcare resource utilization, as measured by the Report of Healthcare Services Form
Data will be summarized using descriptive statistics. Established instruments will be scored according to standard instructions, and appropriate descriptive statistics computed.
Time frame: Up to 2 months
Overall cost, as measured by the Finances and Out of Pocket Costs Tool
Data will be summarized using descriptive statistics. Established instruments will be scored according to standard instructions, and appropriate descriptive statistics computed.
Time frame: Up to 2 months
Patient/family out of pocket expenses, as measured by the Finances and Out of Pocket Costs Tool
Data will be summarized using descriptive statistics. Established instruments will be scored according to standard instructions, and appropriate descriptive statistics computed.
Time frame: Up to 2 months
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