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Effect of a Mobile-Based Anti-Smoking Nursing Intervention on Nursing Students (HDDN)

NCT07429825 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 43

Last updated 2026-02-24

No results posted yet for this study

Summary

This clinical trial aims to understand whether a mobile-based anti-smoking nursing intervention can help nursing students change their smoking-related intentions, attitudes, and decision-making. The study focuses on nursing students who currently smoke.

The main questions this study aims to answer are:

Does the mobile-based nursing intervention reduce nursing students' intention to smoke?

Does the intervention change students' attitudes toward smoking?

Does the intervention affect how students weigh the benefits and harms of smoking when making decisions?

Researchers will compare nursing students who receive the mobile-based anti-smoking nursing intervention with students who do not receive this intervention.

Participants will use a mobile application developed by nurses. Through the application, participants will receive structured nursing support related to smoking prevention. Participants will complete questionnaires about their smoking intentions, attitudes, and decision-making at different time points during the study.

Conditions

  • Tobacco Abuse Cigarette

Interventions

DEVICE

HDDN Mobile Application

The intervention is a mobile-based nursing intervention designed to prevent smoking and support positive health behavior change among nursing students. It is delivered through a smartphone application compatible with iOS and Android operating systems. The intervention includes structured educational modules, motivational messages, and self-monitoring activities focused on smoking-related intention, attitudes, and decision-making balance. Participants receive reminder notifications twice daily during the intervention period. In addition, the application provides nurse-guided support through a messaging feature that allows participants to ask questions and receive guidance. The content of the intervention is based on established behavior change theories and is standardized to ensure that all participants receive the same intervention

Sponsors & Collaborators

  • THE SCİENTİFİC AND TECHNOLOGİCAL RESEARCH COUNCİL OF TURKEY (TUBITAK)

    collaborator UNKNOWN

  • LÜTFİYE GÖKÇE

    lead OTHER

Principal Investigators

  • Şafak Dağhan, PhD, Prof. · Ege University Faculty of Nursing

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
17 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-01
Primary Completion
2025-08-25
Completion
2025-08-25

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 NCT07429825 on ClinicalTrials.gov