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

This study has been terminated.
(Research site no longer available)
Sponsor:
ClinicalTrials.gov Identifier:
NCT01755312
First Posted: December 24, 2012
Last Update Posted: August 27, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Alan Zillich Lab, Purdue University
December 18, 2012
December 24, 2012
August 27, 2015
June 2013
January 2015   (Final data collection date for primary outcome measure)
self-reported medication adherence using the Morisky 8-Item Medication Adherence Scale(MMAS-8) tool [ Time Frame: 6 months ]
medication adherence [ Time Frame: 6 months ]
Complete list of historical versions of study NCT01755312 on ClinicalTrials.gov Archive Site
systolic blood pressure in mmHg using a valid automated device [ Time Frame: 6 months ]
Not Provided
Not Provided
Not Provided
 
The Effect of Medication Reminder Technology on Medication Adherence and Hypertension Outcomes
The Effect of Medication Reminder Technology on Medication Adherence and Hypertension
This study to evaluates how a med reminder affects the patient's ability to take medications as prescribed
Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Health Services Research
  • Medication Adherence
  • Blood Pressure
Device: Medication reminder
Medication reminder
  • Experimental: medication reminder
    medication reminder
    Intervention: Device: Medication reminder
  • Placebo Comparator: Placebo
    Placebo
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
28
January 2015
January 2015   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • poor medication adherence
  • high blood pressure

Exclusion Criteria:

Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01755312
2r44ago39178-02 (1208012596)
No
Not Provided
Not Provided
Alan Zillich Lab, Purdue University
Purdue University
Not Provided
Not Provided
Purdue University
August 2015

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP