Trial Information
Lung Cancer Symptom Assessment and Management Intervention
Inclusion Criteria:
- HCPs: attending physician, thoracic medical oncologist, expected to work in the
setting for at least 2 years.
- Patients: 21 years of age or older; diagnosis of Stage IIIA, IIIB, IV non-small cell
lung cancer OR limited or extensive stage small cell lung cancer; receiving care in
the out-patient setting; receiving treatment with chemotherapy +/- additional
therapies; English speaking.
Exclusion Criteria:
- Patients: Any patient who needs emergent care, routine visits scheduled less than
once a month
Type of Study:
Interventional
Study Design:
Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Outcome Measure:
% completion of intervention use and adherence to suggested symptom management strategies.
Outcome Time Frame:
2 years
Safety Issue:
No
Principal Investigator
Mary E. Cooley, PhD
Investigator Role:
Principal Investigator
Investigator Affiliation:
Dana-Farber Cancer Institute
Authority:
United States: Institutional Review Board
Study ID:
07-404
NCT ID:
NCT00852462
Start Date:
May 2008
Completion Date:
June 2013
Related Keywords:
- Lung Cancer
- SAMI
- Symptom Assessment and Management Intervention Program
- Lung Neoplasms
Name | Location |
Dana-Farber Cancer Institute |
Boston, Massachusetts 02115 |
Boston Medical Center |
Boston, Massachusetts 02118 |