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

F

Fidan Balkaya

Status

Not yet enrolling

Conditions

SLEEP QUALITY
MOBILE WEB-BASED INTERVENTION PROGRAM
NURSING EDUCATION STRESS

Treatments

Behavioral: Mobile based intervention program

Study type

Interventional

Funder types

Other

Identifiers

NCT07138703
Nursing

Details and patient eligibility

About

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.

Enrollment

116 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • PUKI total score above 5
  • Individuals with internet access
  • Owning an Android or iOS phone
  • Those who are open to communication and collaboration

Exclusion criteria

  • Individuals with a psychiatric diagnosis and use of psychiatric medications, according to ASM records,
  • who sleep less than four hours a day, who consume more than four cups of coffee a day
  • who have hearing or balance problems (orthopedic or neurological) will not be included in the study.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

116 participants in 2 patient groups

Intervention Group
Experimental group
Description:
The participants in this group will be using the mobile application
Treatment:
Behavioral: Mobile based intervention program
Control Group
No Intervention group
Description:
The participants in this group will not be using the mobile application

Trial contacts and locations

0

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Central trial contact

Fidan BALKAYA, Research Asistant

Data sourced from clinicaltrials.gov

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