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The Effect of Medication Reminder Technology on Medication Adherence and Hypertension Outcomes

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ClinicalTrials.gov Identifier: NCT01755312
Recruitment Status : Terminated (Research site no longer available)
First Posted : December 24, 2012
Last Update Posted : August 27, 2015
Sponsor:
Information provided by (Responsible Party):
Alan Zillich Lab, Purdue University

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

Condition or disease Intervention/treatment Phase
Medication Adherence Blood Pressure Device: Medication reminder Not Applicable

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 28 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
Official Title: The Effect of Medication Reminder Technology on Medication Adherence and Hypertension
Study Start Date : June 2013
Actual Primary Completion Date : January 2015
Actual Study Completion Date : January 2015

Arm Intervention/treatment
Experimental: medication reminder
medication reminder
Device: Medication reminder
Medication reminder

Placebo Comparator: Placebo
Placebo



Primary Outcome Measures :
  1. self-reported medication adherence using the Morisky 8-Item Medication Adherence Scale(MMAS-8) tool [ Time Frame: 6 months ]

Secondary Outcome Measures :
  1. systolic blood pressure in mmHg using a valid automated device [ Time Frame: 6 months ]


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • poor medication adherence
  • high blood pressure

Exclusion Criteria:


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01755312


Locations
United States, Indiana
Purdue University
West Lafayette, Indiana, United States, 47906
Sponsors and Collaborators
Purdue University

Responsible Party: Alan Zillich Lab, Associate Professor Pharmacy Practice, Purdue University
ClinicalTrials.gov Identifier: NCT01755312     History of Changes
Other Study ID Numbers: 2r44ago39178-02 (1208012596)
First Posted: December 24, 2012    Key Record Dates
Last Update Posted: August 27, 2015
Last Verified: August 2015

Additional relevant MeSH terms:
Hypertension
Vascular Diseases
Cardiovascular Diseases