Electronic Patient Reported Symptom Assessment
Completed · Not applicable
Conditions studied: Gynecologic Cancer, Breast Cancer, Thoracic Cancer, Gastrointestinal Cancer
In brief
The purpose of this study is to assess whether using computerized screening questions can improve how well we manage symptoms related to cancer and cancer treatments. Advance care planning is a process in which teams of experts assist in with treatment plans, managing pain and other symptoms, emotional issues, and end of life issues. With advances in technology, it is now possible to get the patient's feedback directly and more often. It is thought that repeated questionnaires completed by the patient will provide a better and more accurate measure of the patient's needs and experiences but this has not been tested. This study is designed to learn if using a computerized assessment repeatedly is better than standard planning techniques.
Key facts
- Study ID
- NCT01833637
- Run by
- Northwestern University
- People needed
- 6
- Starts
- 2012-10-01
- Expected to finish
- 2015-06-01
- Last updated by the study team
- 2015-07-14
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Women who have a diagnosis of metastatic breast, gynecologic, thoracic, or gastrointestinal malignancy. Women diagnosed with non-solid organ tumors (i.e., lymphoma, leukemia) will be excluded as their symptom profile in advanced/metastatic disease is dissimilar.
- Reason for admission must be for symptom management from cancer or cancer therapy.
- Patients must be age 18 or older.
- Only patients cared for at the Robert H. Lurie Comprehensive Cancer Center (RHLCCC) will be eligible for this small pilot study.
- Patients must not be enrolled in hospice care.
- Patients must have a performance status 0-3 (ECOG scale).
- Patients must be alert and oriented to time, place, and person. Must be able to answer questions.
- Patients must be able to speak, read, and communicate in English.
- Patients must have a signed consent and authorization for research and be amenable to be followed for outcomes/response throughout and after hospitalization.
Where it is running
- Northwestern Memorial Hospital — Chicago, Illinois, United States
Full record on ClinicalTrials.gov
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