Smartphone Use in Healthcare Settings Among Nurses

April 18, 2026 updated by: Mohamed Fakhry Ahmed Salem, Alexandria University

Smartphone Use in Healthcare Settings: Nurses' Messages for Instant Action to Promote Patient Safety; A Cross-sectional Survey With Qualitative Open-ended Questions

This study assessed patterns of smartphone use among nurses and evaluated its impact on clinical performance and patient safety in healthcare settings in Egypt, using a convergent mixed-methods design. A cross-sectional survey was conducted between October 2025 and February 2026 across diverse clinical settings at Alexandria University Hospitals, including critical and emergency care, medical-surgical wards, operating theaters, outpatient clinics, home care services, and psychiatric support units. Of 900 nurses invited, 368 completed the online questionnaire via Google Forms (response rate: 40.9%). Quantitative data assessed nurses' patterns of smartphone use and its impact on patient care using an adapted validated scale. Qualitative data were collected through two open-ended narrative questions exploring smartphone-related clinical incidents and recommendations for safe use. A total of 105 clinical incidents attributed to smartphone distraction were identified and categorized into four themes, while 176 respondents provided actionable recommendations categorized into five strategic pillars for safe clinical integration.

Study Overview

Detailed Description

This study employs a prospective observational design to investigate the integration of smartphone technology in nursing workflows and its direct implications for patient safety. As healthcare environments become increasingly fast-paced, the reliance on instant messaging (e.g., WhatsApp, specialized hospital apps) for clinical communication has grown.

The research focuses on several key dimensions:

Communication Efficiency: Assessing how instant messages facilitate rapid clinical decision-making and "instant action" compared to traditional communication methods.

  • An online self-administered questionnaire will be used for the quantitative part; it will be shared with participants through their personal WhatsApp number after meeting them and getting their approval to participate in the study.
  • Semi-structured interviews will be used to collect data for the qualitative part; interviews will be conducted in the Arabic language, either face-to-face or online through the MS Teams platform (synchronous/asynchronous) mode for easy contact with participants

Patient Safety Outcomes: Monitoring the reporting of critical lab values, medication clarifications, and urgent patient status changes through digital messages.

Workflow Integration: Identifying how nurses prioritize urgent clinical messages amidst their daily responsibilities.

Data collection involves a mixed-methods approach, including the analysis of communication patterns and clinical outcome indicators. The study aims to provide evidence-based insights into how smartphone use can be standardized to minimize risks and maximize the speed of life-saving interventions in hospital settings.

Study Type

Observational

Enrollment (Actual)

368

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Alexandria, Egypt, 21511
        • Faculty of Nursing, Alexandria University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

The study population consists of nurses who are actively providing direct in-patient care in clinical settings. This includes nurses from various departments such as medical-surgical units, intensive care units, and specialized wards. These professionals are primarily those who utilize personal communication devices (PCDs) during their shifts and are capable of reporting their usage patterns and clinical incidents related to patient safety.

Description

Inclusion Criteria:

Device Usage: Must actively use a personal communication device (smartphone or tablet) during working hours for either personal or professional purposes.

Work Setting: Must be assigned to in-patient care units where direct patient monitoring and interaction occur.

Exclusion Criteria:

  • Nurses on leave or those who declined to participate

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Participating Nurses
This arm includes staff nurses to assess their patterns of personal communication device use including frequency, duration, and types of applications while simultaneously evaluating the subsequent impact of these devices on in-patient care. Through a convergent parallel mixed-methods approach, the study examines how these usage patterns influence clinical workflows, nurses' responsiveness, and overall patient safety, focusing on identifying both the professional benefits and potential risks associated with the use of personal devices in clinical settings.

Participants will complete surveys and participate in interviews to assess their patterns of using personal communication devices during work hours. The intervention focuses on identifying frequency, duration, and clinical vs. personal use, as well as evaluating the perceived and actual impact of these behaviors on in-patient care quality and patient safety incidents.

368 nurses from Govermental Hospitals across medical-surgical, critical care, emergency, operating theater, outpatient, home care, and psychiatric settings

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Patterns of Personal Communication Device usage.
Time Frame: October 2025 and February 2026
Evaluation of how frequently and for what duration nurses use their personal devices for both professional and personal purposes during shift hours, measured via a structured survey.
October 2025 and February 2026

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Impact of Personal Communication Device Use on In-patient Care Indicators
Time Frame: October 2025 and February 2026
Assessment of the correlation between device usage patterns and clinical care quality, such as nurses' responsiveness to patient needs and the frequency of reported near-misses or clinical errors related to distraction.
October 2025 and February 2026
Nurses' Perceptions and Reported Clinical Incidents.
Time Frame: October 2025 and February 2026
Qualitative analysis of themes derived from nurses' descriptions of specific incidents and their subjective views on how smartphone messaging facilitates "instant action" or impacts patient safety.
October 2025 and February 2026

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2025

Primary Completion (Actual)

January 1, 2026

Study Completion (Actual)

February 26, 2026

Study Registration Dates

First Submitted

February 21, 2026

First Submitted That Met QC Criteria

March 1, 2026

First Posted (Actual)

March 4, 2026

Study Record Updates

Last Update Posted (Actual)

April 22, 2026

Last Update Submitted That Met QC Criteria

April 18, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared to protect the privacy and confidentiality of the participating nurses

Study Data/Documents

  1. Study Protocol
    Information comments: Available upon request from the Principal Investigator for legitimate research purposes

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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