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The Effect of Mobile Web-based Intervention Programme on Students' Nursing Education Stress and Sleep Quality

NCT07138703 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 116

Last updated 2026-02-24

No results posted yet for this study

Summary

Nursing students experience increased stress and sleep problems due to their demanding academic schedules and the pressures of the clinical environment. Therefore, addressing students' needs for stress and sleep management is critical to improving their educational success. A review of the literature reveals that various interventions are being used to reduce stress levels or improve sleep quality for university students. The purpose of this study is to examine the effects of a web-based intervention program on the stress and sleep levels of nursing students.

This study will utilize a pretest-posttest control group experimental design. The study will be conducted with 120 nursing students enrolled at İnönü University Faculty of Nursing from September 2025 to June 2026. Participants will be administered a Personal Information Form, the Perceived Stress Scale, the Nursing Education Scale, and the Pittsburgh Sleep Quality Index, and the experimental and control groups will be monitored via a mobile application for 12 weeks. Descriptive statistics such as percentages, arithmetic mean (x̄), and standard deviation (SD), along with chi-square and independent samples t-tests, repeated measures t-tests, and Cronbach's alpha will be used for research analyses.

The research is unique in terms of its sample size and the intervention it plans to implement. Therefore, it has the potential to be published in respected international scientific journals. Furthermore, if the effectiveness of the application in managing stress and sleep is established, it is anticipated that it could be applied to other adult populations, particularly midwifery students.

Conditions

  • MOBILE WEB-BASED INTERVENTION PROGRAM
  • NURSING EDUCATION STRESS
  • SLEEP QUALITY

Interventions

BEHAVIORAL

Mobile based intervention program

The participants in this group will be using the mobile application

Sponsors & Collaborators

  • Inonu University

    collaborator OTHER

  • Fidan Balkaya

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-10-01
Primary Completion
2025-11-30
Completion
2026-06-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07138703 on ClinicalTrials.gov