Ambulatory Cancer Pain Management: A Feasibility Study

The primary purpose of this study is to examine the feasibility of collecting pain and other symptom data in outpatient treatment centers across multiple institutions in the Texas Medical Center (TMC). We will also examine the prevalence and severity of cancer-related pain and begin to identify other commonly reported symptoms in outpatient settings. Factors that interfere with management of pain will also be examined. Additionally, the study will explore patient satisfaction with pain management and pain education in outpatient settings. The specific aims of this study include: Primary Objective: -Explore the feasibility of a collaborative effort by oncology nurses to collect pain and symptom data across multiple institutions that care for ambulatory cancer patients in the TMC. Secondary Objectives: * Describe the prevalence and severity of pain and other symptoms in persons with breast, colorectal, lung, or prostate cancer who are receiving chemotherapy in the outpatient setting. * Describe factors that interfere with adequate pain management in these patients. * Examine patient satisfaction with pain management and patient education about pain management.

Sex

All

Minimum age

18 Years

Inclusion Criteria:

1. Diagnosis of breast, colorectal, lung, or prostate cancer (any histological type).
2. Currently undergoing chemotherapy.
3. Age 18 or older.
4. Able to read, write, and speak English.
5. Able to understand the purpose of this study.
6. Must be a patient at one of the four participating institutions.
7. Must be receiving the 2nd, 3rd, or 4th cycle of chemotherapy.

Exclusion Criteria:

1. Receiving chemotherapy in preparation for a bone marrow or stem cell transplant
2. Received a bone marrow or stem cell transplant
3. Age 17 or younger
4. Receiving weekly chemotherapy.
5. Receiving hormonal therapy alone.
6. Receiving radiation or chemoradiation.