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NCT01934608 Clinical Trial

The Effect of Synching Prescription Refills on Adherence

Hypertension Clinical Trial

Official title:
A Randomized Controlled Trial to Test a Synchronized Prescription Refill Program to Improve Medication Adherence

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01934608
Other study ID # HUM-001
Secondary ID
Status Completed
Phase N/A
First received August 29, 2013
Last updated December 21, 2015
Start date September 2013
Est. completion date November 2015

Study information
Verified date December 2015
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

To determine the effect of synchronizing a patient's prescription refill schedule on medication adherence. The targeted population is Humana members who are currently taking 2 or more Stars medications (hypertension, hypercholesterolemia, diabetes) and are current customers of RightSource. Participants will be randomized to one of two groups. Group one will be usual care and group two will be the Rx synchronization group.

Recruitment information / eligibility
Status Completed
Enrollment 691
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Humana members who are currently taking 2 or more Stars medications (hypertension, hypercholesterolemia, diabetes) and are current customers of RightSource.

Exclusion Criteria:

- under 18 years of age

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

Intervention

Behavioral:
• Refill synch

Locations
Country Name City State
United States Humana, Inc Louisville Kentucky

Sponsors (1)
Lead Sponsor Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Medication adherence to each of the chronic medications as measured by the proportion of days covered (PDC) measure 6 months and 12 months No
Secondary Secondary outcomes will be continuous gaps (e.g. 15, 30, or 60 days) in medication use. 6 and 12 months No
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