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The Impact of Pharmacist-led Mobile Application on Adherence in Chronic Kidney Disease Patients

The Impact of Pharmacist - Led Mobile Application on Medication Adherence and Efficacy in Chronic Kidney Disease Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05168449
Enrollment
86
Registered
2021-12-23
Start date
2022-09-17
Completion date
2023-12-05
Last updated
2024-02-09

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

Conditions

Adherence, Medication, Chronic Kidney Diseases

Brief summary

The aim of the study is to assess the impact of pharmacist led mobile application on adherence and efficacy of medication in chronic kidney disease patients

Detailed description

This is a prospective randomized two group pharmacist-led interventional study that will be conducted in a private nephrology clinic. The study will involve introduction of the mobile phone applications to chronic kidney disease patients to improve their adherence to the prescribed medications. Recruited patients will be randomly divided in two groups; intervention group and control group, with baseline evaluation of outcomes to be measured. Control group will be provided with usual care. Intervention group will be provided in addition to the usual care, with an access to the mobile application after a simple training for app usage. Both groups will be followed for a period of 3 months. The study will include the development, validation and the testing for evaluating the specially designed mobile application.

Interventions

OTHERMobile Application

mobile phone applications directed to chronic kidney disease patients to improve their medication.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* Stages 2-5 of chronic kidney disease * Literate * Ownership of android smart phone compatible with the application * Poly-pharmacy

Exclusion criteria

* On dialysis due to loss of kidney function * Pregnancy due to altered physiology

Design outcomes

Primary

MeasureTime frameDescription
Change in medication adherenceChange from baseline at 3 monthsUsing a medication adherence questionnaire.

Secondary

MeasureTime frameDescription
Change in estimated glomerular filtration rate/ creatinine clearanceChange from baseline at 3 monthsCalculated using serum creatinine lab results obtained from clinic.
Change in systolic and diastolic blood pressureChange from baseline at 3 monthsTo be measured in clinic.
Change in HbA1cChange from baseline at 3 monthsLab results obtained from clinic.
Change in mobile application usability and acceptability by patientsChange from baseline at 3 monthsUsing System Usability Scale (SUS) questionnaire. (scale 0-100 with higher score meaning better usability)

Countries

Egypt

Outcome results

None listed

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