Nephrocare mHealth Project: Telemonitoring of Blood Pressure

NCT ID: NCT03708666

Last Updated: 2018-10-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

79 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-06-01

Study Completion Date

2018-06-30

Brief Summary

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The Nephrocare mHealth project supports patients with Chronic Kidney Disease with a mobile application and telemonitoring. The application includes the follow-up of blood pressure.

Detailed Description

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Patients that are included in the Nephrocare mHealth project send their blood pressure results through an app or online website.

The clinical decision support system will alert the patient, as well as the general practitioner and the hospital when the blood pressure is too high or low. In addition the clinical decision support will calculate monthly averages and all the data are connected with the electronic patient files.

Conditions

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Chronic Kidney Diseases Blood Pressure

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Telemonitoring of blood pressure

Patients measure their blood pressure and register their results on the app or website.

Group Type OTHER

Telemonitoring of blood pressure

Intervention Type OTHER

Blood pressure monitoring at least once a week.

Interventions

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Telemonitoring of blood pressure

Blood pressure monitoring at least once a week.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Dutch-speaking
* Signed and approved informed consent
* Follow-up by nephrology at the University Hospitals Leuven or General Hospital Groeninge

Exclusion Criteria

* No Dutch-speaking
* Impaired cognitive condition or medically unstable
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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General Hospital Groeninge

OTHER

Sponsor Role collaborator

Universitaire Ziekenhuizen KU Leuven

OTHER

Sponsor Role lead

Responsible Party

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Kathleen Claes

Prof. Dr. K. Claes

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Kathleen Claes, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

Universitaire Ziekenhuizen KU Leuven

Locations

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University Hospitals Leuven

Leuven, , Belgium

Site Status

Countries

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Belgium

Other Identifiers

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AZGS2017056

Identifier Type: OTHER

Identifier Source: secondary_id

S60335

Identifier Type: -

Identifier Source: org_study_id

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