Skip to content

mHealth for Phosphorus Management in CKD.

mHealth System for the Self-control of Hyperphosphatemia in Patients With CKD.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05389826
Acronym
PHOSFO_OK
Enrollment
50
Registered
2022-05-25
Start date
2022-06-01
Completion date
2023-10-15
Last updated
2023-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dialysis Related Complication

Keywords

mHealth, Hyperphosphatemia

Brief 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).

Detailed 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.

Interventions

We will compare the degree of improvement in phosphate control with respect to baseline values and report any adverse event. Nephrologist will use a web management system to provide results of phosphorus levels and medical recommendations to the patient, mediated by a cloud IT environment. In addition, patients will receive alerts, suggestions, and general information. They will also be able to communicate with nephrologists and interact with their corresponding group of fellow patients.

Sponsors

Vifor Pharma
CollaboratorINDUSTRY
Hospital Universitari de Bellvitge
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Pilot study involving cases and controls. Fifty outpatient patients with stage 4-5 CKD, including those on dialysis will be included. Twenty-five patients will be followed with the developed mobile web app, while another twenty-five patients will be treated according to the current clinical practice. Patients will be randomized blindly 1:1 to the study group or to the control group. The randomization technique consists of consecutively numbered sealed envelopes on which the signed group is written.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1- Eligible patients will be stage 4-5 CKD patients, including end-stage renal disease (ESRD) on dialysis, aged \>18 with hyperphosphatemia (serum phosphorus concentration \>1.94 mmol/L) and stable dose of phosphate binders for \>1 month before screening.

Exclusion criteria

1. Patients with intact parathyroid hormone concentration \>800 ng/l (88 pmol/l) or if parathyroidectomy will be planned or expected. 2. Patients with significant gastro-intestinal (GI) or hepatic disorders. 3. Patients with major GI surgery.

Design outcomes

Primary

MeasureTime frameDescription
Analysis of the superiority of mobile-app and benchmarking versus standard of care in lowering serum phosphorus6-months follow-upReduction of serum phosphorus by more than 0.5 mmol/L versus the standard of care testing.

Secondary

MeasureTime frameDescription
Adherence to phosphate binder's use and reduction in their use.6-months follow-upThe ratio of current phosphate binders that the patient is swallowing compared to the number prescribed.
Quality of life improvement6-months follow-upHealth-related quality of life (HRQoL) will be assessed with the Short-Form 12 questionnaire (SF-12).
Patient's and healthcare professionals' satisfaction with mobile health app to ensure its usability and promote patient retention6-months follow-upSatisfaction of patients will be assessed with the quality of care satisfaction in outpatient consultation questionnaire (EQS-C).

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026