Clinical Trials Logo

Clinical Trial Summary

The project aims to generate an mHealth environment in which CKD patients are empowered in terms of the self-management of their hyperphosphatemia pathology, while under medical supervision. Such environment will allow nephrologists to inform patients beyond their traditional point-of-care and will allow patients to provide feedback on their condition in a timely manner that benefits the CKD collective. In this way we delve in a technological area that has been argued that remains underutilized within nephrology (1) and that should be perceived as an opportunity for CKD (2). In our work, we will build from recent related efforts in the control of hyperphosphatemia (3).


Clinical Trial Description

The working hypotheses are listed as follows: 1. Hyperphosphatemia is an important problem in the CKD realm, but difficult to manage because patients are often not aware of its importance. In addition, current clinical practice does not allow nephrologists to evaluate the patient's real understanding of their recommendations. 2. The patient could benefit from a smartphone-based interactive virtual assistant tool: an integrated personalized management system to achieve a form of participatory, personalized, predictive and preventive medicine in the specific domain of a pathology associated to CKD. 3. The combination of a flexible information channel with an interactive data visualization tool on mobile devices can be a most intuitive way to communicate with the patient, particularly if it allows comparison with other patients in similar situation. Additionally, data visualization can assist nephrologists in the clinical management of patients. Primary Objective: 1-Analysis of the superiority of a Medical Mobile Application for Patient Support to educate CKD patients on how to self-manage their phosphate levels versus standard of care in lowering serum phosphorus by assessing changes in serum phosphorus comparing baseline with 6-months follow-up. Secondary Objectives: 1. Adherence to treatment with phosphate binders. 2. Impact in Quality of Life of patients with CKD. 3. Satisfaction of such a tool. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05389826
Study type Interventional
Source Hospital Universitari de Bellvitge
Contact
Status Active, not recruiting
Phase N/A
Start date June 1, 2022
Completion date October 15, 2023

See also
  Status Clinical Trial Phase
Completed NCT03836508 - Effect of Dialysis Membranes on Inflammatory and Immune Processes in Hemodialysis N/A
Completed NCT03274518 - Expanded Hemodialysis Versus Online Hemodiafiltration N/A
Completed NCT03211676 - Comparison of Hemodialysis With Medium Cut-off Dialyzer (Theranova) and High Flux Dialyzer N/A
Active, not recruiting NCT03976440 - Simplified Regional Citrate Anticoagulation Protocols for CVVH, CVVHDF and SLED: a Pilot Study
Completed NCT03927300 - Telemonitoring Impact by the ApTelecare Software in Dialysis Patient
Recruiting NCT04218370 - Liberation From Acute Dialysis N/A
Completed NCT03202212 - Effect of Mixed On-line Hemodiafiltration on Circulating Markers of Inflammation and Vascular Dysfunction Phase 1/Phase 2
Not yet recruiting NCT06233838 - Multi-center Clinical Study on Hemoperfusion of KHA80 N/A
Recruiting NCT03674307 - Screening for Asymptomatic Coronary Artery Disease in Kidney Transplant Candidates N/A
Recruiting NCT03990818 - Continuous Registration of Bioimpedance During Hemodialysis
Active, not recruiting NCT04796558 - Validation of Arterio Venous Access Stage (AVAS) Classification