Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
22 participants
OBSERVATIONAL
2013-11-30
2015-04-30
Brief Summary
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Detailed Description
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The first initial meeting will be conducted at a time and location that is convenient for the patient. This meeting should last about an hour to an hour and a half.
Three and six months after the initial interview, study participants will be asked to complete a follow-up survey by either telephone or Internet/Web, depending on their preference. These telephone surveys will last between 15-30 minutes.
Conditions
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Study Design
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PROSPECTIVE
Study Groups
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Working Poor Survivors
Low Wage workers
No interventions assigned to this group
Non-Working Poor Survivors
Higher-Wage Salary Workers
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Working at least 20 hours per week
* Currently patients of the University of Kentucky Markey Cancer Center
* Are able to read, write, and communicate in English
* Have reliable telephone or Internet/Web access in or outside the home
Exclusion Criteria
* Unemployed
* Cognitively impaired
18 Years
65 Years
FEMALE
No
Sponsors
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National Institute on Drug Abuse (NIDA)
NIH
Robin Vanderpool
OTHER
Responsible Party
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Robin Vanderpool
Principal Investigator
Principal Investigators
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Robin Vanderpool, DrPH
Role: PRINCIPAL_INVESTIGATOR
University of Kentucky
Locations
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UK Center for Clinical and Translational Science
Lexington, Kentucky, United States
University of Kentucky Markey Cancer Center
Lexington, Kentucky, United States
Countries
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Other Identifiers
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IRB # 13-0560-P3H
Identifier Type: -
Identifier Source: org_study_id
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