Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04098354

Telemonitoring of Hypertensive Patients With Chronic Kidney Disease

Led by University of Alberta · Updated on 2025-09-18

146

Participants Needed

1

Research Sites

245 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Background: Hypertension, together with poorly controlled blood pressure (BP) are known risk factors for kidney disease and progression to kidney failure as well as increased cardiovascular (CV) morbidity and mortality. Several studies in patients without kidney disease have demonstrated the efficacy of home BP telemonitoring (HBPT) for BP control. Objective: The primary aim of this study is to assess the mean difference in systolic BP (SBP) at 12 months, from baseline in remote dwelling patients with hypertension and chronic kidney disease (CKD) in Northern Alberta, Canada, comparing HBPT + usual care versus HBPT + a case manager. Other secondary objectives, including cost-effectiveness and acceptability of HBPT as well as occurrence of adverse events will also be assessed. Methods Design: This study is designed as a pragmatic randomized controlled trial (RCT) of HBPT plus clinical case management compared to HBPT with usual care. Setting: Peace River region in Northern Alberta Region, Canada. Patients: Primary care patients with CKD and hypertension. Measurements: Eligible patients will be randomized 1:1 to HBPT + BP case management versus HBPT + usual care. In the intervention arm, BP will be measured 4 times daily for 1 week, with medications titrated up or down by the study case manager until guideline targets (systolic BP \[SBP\]: \<130mmHg) are achieved. Once BP is controlled, (i.e., to guideline-concordant targets), this 1-week protocol will be repeated every 3 months for 1 year. Patients in the control arm will also follow the same BP measurement protocol, however, there will be no interactions with the case manager; they will share their BP readings with their primary care physicians or nurse practitioners at scheduled visits. Limitations: Potential limitations of this study include the relatively short duration of follow-up, possible technological pitfalls, and need for patients to own a smartphone and have access to the internet to participate. Conclusions: As this study will focus on a high-risk population that has been characterized by a large care gap, it will generate important evidence that would allow targeted and effective population-level strategies to be implemented to improve health outcomes for high-risk hypertensive CKD patients in Canada's remote communities.

CONDITIONS

Official Title

Telemonitoring of Hypertensive Patients With Chronic Kidney Disease

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older with documented chronic kidney disease (eGFR less than 60 mL/min/1.73m2 and/or proteinuria greater than 1 g/day)
  • Living in the remote Peace River region of Alberta, Canada
  • Diagnosed with hypertension and currently taking blood pressure medication
  • Own a smartphone (iOS or Android) with wireless internet access
  • Able to speak and write in English and willing to provide informed consent
  • Able and willing to use the home blood pressure telemonitoring device with at least 80% of recordings sent during training
Not Eligible

You will not qualify if you...

  • Experiencing hypertensive urgency or emergency during training
  • Having stage 5 chronic kidney disease (eGFR 15 mL/min/1.73m2 or less) or receiving kidney replacement therapy
  • Diagnosed with heart failure with reduced ejection fraction
  • Having any terminal illness with life expectancy less than one year
  • Currently participating in another clinical drug trial
  • Pregnant or breastfeeding
  • Planning to move out of the Peace River region or living in an area without mobile phone coverage

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Alberta

Edmonton, Albert, Canada, T6G 2C8

Actively Recruiting

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Research Team

D

Deenaz Zaidi

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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Telemonitoring of Hypertensive Patients With Chronic Kidney Disease | DecenTrialz