Measurement of Pain and Other Symptoms of Non-Small Cell Lung Cancer (NSCLC) Patients Following Thoracic Surgery
Completed
Conditions studied: Lung Cancer
In brief
Primary Objectives: * To longitudinally assess the natural history of symptoms (prevalence, severity, patterns of symptoms, and the relationship of physical and psychological distress) among post-thoracic surgery for non-small cell lung cancer patients with early stage (stage I-IIIA) disease. * To determine crisis events (when symptoms are most severe), their relationship with cancer therapy, surgical techniques and disease, and their relationship with function and quality of life; and to determine current practice patterns of symptom control throughout the six months of the post-surgical phase. * To determine the utility of a weekly, telephone-administered interactive voice response symptom assessment (IVR-MDASI) for identifying emergent clinically significant symptoms in this population. * To develop symptom severity critical values and critical treatment algorithms for post-operative symptom control for NSCLC patients.
Key facts
- Study ID
- NCT00501319
- Run by
- M.D. Anderson Cancer Center
- People needed
- 127
- Starts
- 2003-04-01
- Expected to finish
- 2011-10-01
- Last updated by the study team
- 2011-11-08
Who can join
Age: 16 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients scheduled for thoracic surgery for NSCLC (stage I-IIIA)
- Patients >/= 16 years of age
- Patients who speak English
- Patients residing in the United States
You may not qualify if…
- Current diagnosis of psychosis or dementia
- Patients who have difficulty understanding the intent of the study
- Patients who can not complete the assessment tools
- Patients without telephone access
Where it is running
- UT MD Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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