The Effect of Synching Prescription Refills on Adherence
NCT ID: NCT01934608
Last Updated: 2015-12-22
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
NA
691 participants
INTERVENTIONAL
2013-09-30
2015-11-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
PREVENTION
NONE
Study Groups
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Refill synch
Participants in this group will have their medication refill schedule synchronized.
Refill synch
Control
Participants in this arm will receive usual care
No interventions assigned to this group
Interventions
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Refill synch
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
65 Years
ALL
Yes
Sponsors
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University of Pennsylvania
OTHER
Responsible Party
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Principal Investigators
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Jalpa Doshi, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Pennsylvania
Locations
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Humana, Inc
Louisville, Kentucky, United States
Countries
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Other Identifiers
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HUM-001
Identifier Type: -
Identifier Source: org_study_id