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Clinical Trials/NCT01963156
NCT01963156TerminatedNot Applicable

Synchronization to Improve Non-Adherence to Cardiovascular Medications (SyNCMed)

Brigham and Women's Hospital2 sites in 1 country3,675 target enrollmentStarted: November 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Terminated
Enrollment
3,675
Locations
2
Primary Endpoint
Medication adherence

Study Overview

Brief Summary

The aim of this study is to evaluate if synchronizing when patients with diabetes and/or coronary artery disease fill their prescriptions improves long-term adherence to these medications.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Medication adherence

Time Frame: 12 months

Average adherence to medications for the treatment of cardiovascular disease and diabetes medications as assessed using administrative pharmacy claims

Secondary Outcomes

  • Full adherence to medications for the treatment of diabetes or cardiovascular disease(12 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Niteesh K. Choudhry, MD, PhD

Associate Professor, Harvard Medical School

Brigham and Women's Hospital

Study Sites (2)

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