NCT01755312

Brief Summary

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

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
28

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2013

Geographic Reach
1 country

1 active site

Status
terminated

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 18, 2012

Completed
6 days until next milestone

First Posted

Study publicly available on registry

December 24, 2012

Completed
5 months until next milestone

Study Start

First participant enrolled

June 1, 2013

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2015

Completed
Last Updated

August 27, 2015

Status Verified

August 1, 2015

Enrollment Period

1.6 years

First QC Date

December 18, 2012

Last Update Submit

August 26, 2015

Conditions

Medication AdherenceBlood Pressure

Outcome Measures

Primary Outcomes (1)

  • self-reported medication adherence using the Morisky 8-Item Medication Adherence Scale(MMAS-8) tool

    6 months

Secondary Outcomes (1)

  • systolic blood pressure in mmHg using a valid automated device

    6 months

Study Arms (2)

medication reminder

EXPERIMENTAL

medication reminder

Device: Medication reminder

Placebo

PLACEBO COMPARATOR

Placebo

Interventions

Medication reminderDEVICE

Medication reminder

medication reminder

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • poor medication adherence
  • high blood pressure

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Purdue University

West Lafayette, Indiana, 47906, United States

Location

MeSH Terms

Conditions

Medication Adherence

Condition Hierarchy (Ancestors)

Patient CompliancePatient Acceptance of Health CareTreatment Adherence and ComplianceHealth BehaviorBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor Pharmacy Practice

Study Record Dates

First Submitted

December 18, 2012

First Posted

December 24, 2012

Study Start

June 1, 2013

Primary Completion

January 1, 2015

Study Completion

January 1, 2015

Last Updated

August 27, 2015

Record last verified: 2015-08

Locations

US(1)