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Clinical Trials/NCT00852462
NCT00852462
Completed
Phase 2

Lung Cancer Symptom Assessment and Management Intervention

Dana-Farber Cancer Institute2 sites in 1 country179 target enrollmentMay 2008
ConditionsLung Cancer

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Lung Cancer
Sponsor
Dana-Farber Cancer Institute
Enrollment
179
Locations
2
Primary Endpoint
% completion of intervention use and adherence to suggested symptom management strategies.
Status
Completed
Last Updated
9 years ago

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).

Registry
clinicaltrials.gov
Start Date
May 2008
End Date
June 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mary E. Cooley, Phd

Nurse Scientist

Dana-Farber Cancer Institute

Eligibility Criteria

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)

Study Sites (2)

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