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NCT03708666 Clinical Trial

Nephrocare mHealth Project: Telemonitoring of Blood Pressure

Blood Pressure Clinical Trial

— Nephrocare  

Official title:
Nephrocare mHealth: Improvement of Patient Empowerment and Self-management by the Use of Telemonitoring.

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03708666
Other study ID # S60335
Secondary ID AZGS2017056
Status Completed
Phase N/A
First received
Last updated
Start date June 1, 2017
Est. completion date June 30, 2018

Study information
Verified date October 2018
Source Universitaire Ziekenhuizen Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility
Status Completed
Enrollment 79
Est. completion date June 30, 2018
Est. primary completion date December 31, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Telemonitoring of blood pressure
Blood pressure monitoring at least once a week.

Locations
Country Name City State
Belgium University Hospitals Leuven Leuven

Sponsors (2)
Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven General Hospital Groeninge

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary Systolic and diastolic blood pressure under control Percentage of patients with blood pressure within target limits 6 months
Secondary Adaptations of treatment Percentage of change in hypertension therapy 6 months
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