NCT00852462CompletedPhase 2
Lung Cancer Symptom Assessment and Management Intervention
Conditions
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Sponsor
- Dana-Farber Cancer Institute
- Enrollment
- 179
- Locations
- 4
- Primary Endpoint
- % completion of intervention use and adherence to suggested symptom management strategies.
Study Overview
Brief Summary
The purpose of this study is to develop and test the usability of a computerized symptom assessment and management intervention system in a laboratory setting (phase I) and its feasibility in a clinical setting in a group randomized trial (phase II).
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- None
Eligibility Criteria
- Ages
- 21 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
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
Outcomes
Primary Outcomes
% completion of intervention use and adherence to suggested symptom management strategies.
Time Frame: 2 years
Secondary Outcomes
- Health-related quality of life(6 months)
Investigators
Mary E. Cooley, Phd
Nurse Scientist
Dana-Farber Cancer Institute
Study Sites (4)
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