Suspended

HTNmobileImproving Medication Adherence in Hypertensive Patients

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Electronic Intervention

Behavioral
Who is being recruted

Cardiovascular Diseases

+ Vascular Diseases

+ Hypertension

From 18 to 75 Years
+15 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Services Research Study

Interventional
Study Start: January 2014
See protocol details

Summary

Principal SponsorDuke University
Last updated: January 28, 2014
Sourced from a government-validated database.Claim as a partner

Study start date: January 1, 2014

Actual date on which the first participant was enrolled.

The intervention will incorporate a scalable electronic intervention using Email/Web Apps and Short Message Service (SMS)/Mobile Web Apps. The study team will examine the participants' responses to the electronic encounters in the technology-only intervention throughout the 3-month study timeframe.

NCT01826435
Principal SponsorDuke University
Last updated: January 28, 2014
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Services Research Study

These studies look at how healthcare is delivered, managed, and organized. They aim to improve care quality, patient experience, and access to treatment.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 75 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Cardiovascular DiseasesVascular DiseasesHypertension

Criteria

3 inclusion criteria required to participate
Enrolled in the primary care clinic for the past 6 months
New or existing prescription for hypertension
Poorly controlled mean systolic blood pressure (SBP) in the last 12 months ( > 140/90 Hg)
12 exclusion criteria prevent from participating
Active diagnosis of psychosis or dementia documented in medical record
Another household member enrolled in study
Arm size > 50cm
Diagnosis of metastatic cancer
Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Over the three months, participants will receive a technology intervention. This will include text or email encounter notifications associated with appropriate mobile or online self-management information for medication adherence and behavior change.

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Duke University Health System Clinic

Durham, United StatesOpen Duke University Health System Clinic in Google Maps
SuspendedOne Study Center