search
Back to results

mHealth for Phosphorus Management in CKD. (PHOSFO_OK)

Primary Purpose

Dialysis Related Complication

Status
Active
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
mHealth App
Sponsored by
Hospital Universitari de Bellvitge
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Dialysis Related Complication focused on measuring mHealth, Hyperphosphatemia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Hospital Bellvitge

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

mHealth App group

Control

Arm Description

Patients will be followed with the developed mobile web app,

Patients will be treated according to the current clinical practice.

Outcomes

Primary Outcome Measures

Analysis of the superiority of mobile-app and benchmarking versus standard of care in lowering serum phosphorus
Reduction of serum phosphorus by more than 0.5 mmol/L versus the standard of care testing.

Secondary Outcome Measures

Adherence to phosphate binder's use and reduction in their use.
The ratio of current phosphate binders that the patient is swallowing compared to the number prescribed.
Quality of life improvement
Health-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 retention
Satisfaction of patients will be assessed with the quality of care satisfaction in outpatient consultation questionnaire (EQS-C).

Full Information

First Posted
May 13, 2022
Last Updated
September 20, 2023
Sponsor
Hospital Universitari de Bellvitge
Collaborators
Vifor Pharma
search

1. Study Identification

Unique Protocol Identification Number
NCT05389826
Brief Title
mHealth for Phosphorus Management in CKD.
Acronym
PHOSFO_OK
Official Title
mHealth System for the Self-control of Hyperphosphatemia in Patients With CKD.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 1, 2022 (Actual)
Primary Completion Date
October 15, 2023 (Anticipated)
Study Completion Date
October 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital Universitari de Bellvitge
Collaborators
Vifor Pharma

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

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: 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. 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. 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: Adherence to treatment with phosphate binders. Impact in Quality of Life of patients with CKD. Satisfaction of such a tool.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dialysis Related Complication
Keywords
mHealth, Hyperphosphatemia

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
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.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
mHealth App group
Arm Type
Experimental
Arm Description
Patients will be followed with the developed mobile web app,
Arm Title
Control
Arm Type
No Intervention
Arm Description
Patients will be treated according to the current clinical practice.
Intervention Type
Device
Intervention Name(s)
mHealth App
Intervention Description
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.
Primary Outcome Measure Information:
Title
Analysis of the superiority of mobile-app and benchmarking versus standard of care in lowering serum phosphorus
Description
Reduction of serum phosphorus by more than 0.5 mmol/L versus the standard of care testing.
Time Frame
6-months follow-up
Secondary Outcome Measure Information:
Title
Adherence to phosphate binder's use and reduction in their use.
Description
The ratio of current phosphate binders that the patient is swallowing compared to the number prescribed.
Time Frame
6-months follow-up
Title
Quality of life improvement
Description
Health-related quality of life (HRQoL) will be assessed with the Short-Form 12 questionnaire (SF-12).
Time Frame
6-months follow-up
Title
Patient's and healthcare professionals' satisfaction with mobile health app to ensure its usability and promote patient retention
Description
Satisfaction of patients will be assessed with the quality of care satisfaction in outpatient consultation questionnaire (EQS-C).
Time Frame
6-months follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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: Patients with intact parathyroid hormone concentration >800 ng/l (88 pmol/l) or if parathyroidectomy will be planned or expected. Patients with significant gastro-intestinal (GI) or hepatic disorders. Patients with major GI surgery.
Facility Information:
Facility Name
Hospital Bellvitge
City
L'Hospitalet de Llobregat
State/Province
Barcelona
ZIP/Postal Code
08907
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Reporting the study design
IPD Sharing Time Frame
3 months
IPD Sharing Access Criteria
Publication
Citations:
PubMed Identifier
35498887
Citation
Stauss M, Dhaygude A, Ponnusamy A, Myers M, Woywodt A. Remote digital urinalysis with smartphone technology as part of remote management of glomerular disease during the SARS-CoV-2 virus pandemic: single-centre experience in 25 patients. Clin Kidney J. 2021 Dec 21;15(5):903-911. doi: 10.1093/ckj/sfab286. eCollection 2022 May.
Results Reference
background
PubMed Identifier
30898874
Citation
Topf JM, Hiremath S. Got CKD? There's an App for That! Clin J Am Soc Nephrol. 2019 Apr 5;14(4):491-492. doi: 10.2215/CJN.02350219. Epub 2019 Mar 21. No abstract available.
Results Reference
background
PubMed Identifier
33251815
Citation
Chiang YC, Chang YP, Lin SC, Lin C, Hsu PH, Hsu YJ, Wu TJ. Effects of Individualized Dietary Phosphate Control Program With a Smartphone Application in Hemodialysis Patients in Taiwan. Biol Res Nurs. 2021 Jul;23(3):375-381. doi: 10.1177/1099800420975504. Epub 2020 Nov 28.
Results Reference
background

Learn more about this trial

mHealth for Phosphorus Management in CKD.

We'll reach out to this number within 24 hrs