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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01755312
Other study ID # 2r44ago39178-02 (1208012596)
Secondary ID
Status Terminated
Phase N/A
First received December 18, 2012
Last updated August 26, 2015
Start date June 2013
Est. completion date January 2015

Study information

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

Clinical Trial Summary

This study to evaluates how a med reminder affects the patient's ability to take medications as prescribed


Recruitment information / eligibility

Status Terminated
Enrollment 28
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- poor medication adherence

- high blood pressure

Exclusion Criteria:

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Device:
Medication reminder
Medication reminder

Locations

Country Name City State
United States Purdue University West Lafayette Indiana

Sponsors (1)

Lead Sponsor Collaborator
Purdue University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary self-reported medication adherence using the Morisky 8-Item Medication Adherence Scale(MMAS-8) tool 6 months Yes
Secondary systolic blood pressure in mmHg using a valid automated device 6 months No
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