CClinicalTrials.gg
CompletedNCT01952119Updated Sep 27, 2013

Effect of a Secure Message Reminder on Hypertension Follow-up at an Integrated Health Care System

An interventional study of Secure message reminder in Hypertension, sponsored by Kaiser Permanente. Completed at 1 site in United States. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2013-09-27.

Sponsored by Kaiser Permanente · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
182
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This study will assess whether adding a secure message reminder to routine care improves the percentage of patients who complete a follow-up appointment with a new, documented blood pressure reading.

Read the detailed description

Hypertension is one of the leading risk factors for cardiovascular disease. Optimizing blood pressure management can help prevent adverse cardiovascular outcomes. The National Committee for Quality Assurance (NCQA) defines blood pressure control as less than 140/90 mmHg. Per this definition, less than half of Americans with hypertension are considered controlled. Literature has been published describing several ways of improving blood pressure management, but results have been variable.

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Conditions studied

  • Hypertension

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Keywords

  • hypertension
03

In context

Hypertension

6,689 studies on the registry are indexed under Hypertension; 965 are open to participants now.

This study's enrollment of 182 is above the median of 90 across 4,995 interventional studies indexed under Hypertension.

Browse Hypertension studies →

Lead sponsor

Kaiser Permanente is the lead sponsor of 385 studies on the registry; 41 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 3 (50%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Member of Kaiser Permanente Georgia Pharmacy Cardiac Risk Service (PCRS)
  • 18-75 years of age
  • Enrolled in http://kp.org
  • Most recent documented blood pressure is greater than or equal to 140/90 mmHg

Exclusion criteria

Exclusion Criteria:

  • Most recent documented blood pressure is greater than or equal to 180/110 mmHg
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Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
182 participants (actual)

Study arms

  • No intervention
    Routine Care

    Routine care, no intervention

  • Active comparator
    Secure message reminder

    Will receive a secure message reminder asking subjects to schedule an appointment with their provider or make a nurse visit to follow-up on their blood pressure

    Other: Secure message reminder

Interventions

  • OtherSecure message reminder

    Single secure message reminder asking subjects to schedule an appointment with their provider or make a nurse visit to follow-up on their blood pressure

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What researchers measure

Primary outcomes

  1. Appointment with new blood pressure reading

    Percentage of patients who complete an appointment with a new documented blood pressure reading within six weeks after distributing the secure message reminder

    Time frame: 6 weeks

Secondary outcomes

  1. New appointment with new blood pressure reading

    Time frame: 6 weeks

  2. Existing appointment kept with new blood pressure reading

    Time frame: 6 weeks

  3. Change in antihypertensive regimen

    Time frame: 6 weeks

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Study locations

1 site
  • Kaiser Permanente Georgia
    Atlanta, Georgia 30305, United States
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References and documents

Publications

  • Glynn LG, Murphy AW, Smith SM, Schroeder K, Fahey T. Interventions used to improve control of blood pressure in patients with hypertension. Cochrane Database Syst Rev. 2010 Mar 17;(3):CD005182. doi: 10.1002/14651858.CD005182.pub4. PubMed 20238338 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 27, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01952119
Lead sponsor
Kaiser Permanente
Responsible party
Sponsor
First posted
Sep 27, 2013
Start date
Oct 2011
Primary completion
Dec 2011
Completion
Jun 2012
Last update
Sep 27, 2013

Study contacts

Alina Kuo, PharmD
principal investigator · Kaiser Permanente Georgia
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2013. You cannot join it, but the record below documents what was studied.

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