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Starting soon Not applicable

Digital Application-Based Nursing Intervention

NCT07701057 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-07-15
Last updated
2026-07-14

Condition(s) studied

Kidney Transplantation

Investigational drug(s) / intervention(s)

Digital Application-Based Nursing Intervention

Digital Application-Based Nursing Intervention: A multi-component, digital application-based nursing intervention designed to improve post-transplant health outcomes. The intervention consists of two main components: 1) The MyTherapy smartphone application, utilized by patients to receive tailored medication reminders, track post-operative symptoms, and maintain daily health logs. 2) A comprehensive, illustrated educational booklet written in simple Arabic to guide patients on essential post-transplant self-care, medication compliance, vital signs self-monitoring, and necessary lifestyle modifications.

Study summary

The purpose of this study is to evaluate the effect of a digital application-based nursing intervention on improving health outcomes among kidney transplant recipients. Following kidney transplantation, patients face critical, lifelong challenges that require strict adherence to immunosuppressive therapy and rigorous self-management behaviors to prevent graft rejection and mortality. This study introduces a dual-component nursing intervention comprising an illustrated educational booklet and the implementation of the "MyTherapy" mobile health application. The study aims to determine whether combining tailored patient education with real-time digital medication reminders and symptom tracking can successfully enhance medication adherence, improve daily self-management behaviors, and reduce the self-perceived burden among transplant recipients during their post-operative recovery phase.

Eligibility

Sex
ALL
Min age
20 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Adult kidney transplant recipients (aged 20-65 years). * Patients transplanted between June 2024 and June 2026 who are currently maintained on regular outpatient follow-up. * Patients who have access to a smartphone compatible with the mobile application. Exclusion Criteria: * Patients and family members who are illiterate or unable to use the mobile application effectively due to literacy limitations. * Patients with severe cognitive impairment or psychiatric conditions * Patients with auditory and visual disorders. * Patients with failed graft. * Patients who are lost to follow-up.

Primary outcome measure(s)

  • Change in Medication Adherence — Baseline, 1 month, and 3 months post-intervention
    Medication adherence will be assessed using the 8-item Morisky Medication Adherence Scale (MMAS-8). Total scores range from 0 to 8, where higher scores indicate better adherence levels (high adherence = 8, medium adherence = 6 to \<8, low adherence = \<6).

Trial sites (1)

FacilityCityRegionStatus
Assiut University Urology Hospital Asyut Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07701057 on ClinicalTrials.gov ↗ ← All trials in Egypt