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AI-Supported Gamified Training for Sharps Injury Prevention in Nurses

26. april 2026 opdateret af: İsmail Kuşoğlu, Baskent University

The Effect of An Artifıcial Intelligence-Supported Gamifıed Training Program on Nurses' Knowledge and Attitudes Toward The Prevention of Sharps Injuries

This study aims to evaluate the effect of a Health Belief Model (HBM)-based, artificial intelligence (AI)-supported gamified training program on nurses' knowledge and attitudes toward the prevention of sharps injuries. Sharps injuries remain a significant occupational risk for healthcare workers, particularly nurses, despite existing standard precautions.

The study will be conducted in two phases. In the first phase, the validity and reliability of the Sharps Injury Prediction Scale will be tested in a nurse population. In the second phase, a quasi-experimental pretest-posttest control group design will be used to assess the effectiveness of the intervention.

The study will be carried out in two hospitals from the same healthcare group located in different cities to prevent interaction between groups. A total of 36 nurses will be included, with 18 participants in the intervention group and 18 in the control group.

The intervention group will receive a structured, HBM-based training program consisting of seven sessions incorporating AI-supported content, gamified scenarios, interactive materials, and feedback mechanisms to enhance engagement and promote behavior change. The control group will receive routine institutional training on sharps injury prevention.

Data will be collected at baseline, immediately after the intervention, and two months later. Outcome measures include nurses' knowledge, attitudes toward safe sharps use, and sharps injury risk perception.

It is expected that the AI-supported gamified training program will significantly improve knowledge, attitudes, and risk awareness compared to routine training. The findings may support the integration of innovative, theory-based educational interventions into institutional training programs to enhance occupational safety.

Studieoversigt

Detaljeret beskrivelse

Sharps injuries are among the most common occupational hazards for healthcare workers, particularly nurses, due to their frequent exposure to invasive procedures and contact with blood and body fluids. These injuries are associated with the risk of transmission of serious infections such as hepatitis B, hepatitis C, and HIV. Despite the implementation of standard precautions and institutional training programs, the incidence of sharps injuries remains a significant concern, highlighting the need for more effective and behavior-focused educational interventions.

Traditional training methods are often limited in their ability to promote sustained behavioral change. In this context, theory-based and technology-supported approaches may provide more effective solutions. The Health Belief Model (HBM) is widely used to explain and predict health-related behaviors by focusing on individuals' perceptions of risk, benefits, barriers, and self-efficacy. Integrating HBM into educational interventions may enhance the effectiveness of training programs aimed at improving safe practices.

In addition, recent advances in artificial intelligence (AI) and gamification have introduced innovative opportunities in health education. AI-supported systems can provide personalized learning experiences, while gamification techniques, such as interactive scenarios, feedback, and rewards, can increase motivation, engagement, and knowledge retention. These approaches may be particularly beneficial in nursing education, where active participation and behavioral reinforcement are essential.

This study will be conducted in two phases. In the first phase, the validity and reliability of the Sharps Injury Prediction Scale will be evaluated in a nurse population. In the second phase, a quasi-experimental pretest-posttest control group design will be used to assess the effectiveness of an HBM-based, AI-supported gamified training program.

The study will be carried out in two hospitals within the same healthcare group located in different cities to minimize interaction between groups. A total of 36 nurses will be included. The intervention group will receive a structured training program consisting of seven sessions designed based on HBM constructs, incorporating AI-supported educational materials, gamified learning tools, and interactive components. The control group will receive routine institutional training.

Data will be collected at baseline, immediately after the intervention, and two months after the intervention. Outcome measures will include knowledge levels, attitudes toward safe use of sharps, and risk perception related to sharps injuries.

The findings of this study are expected to contribute to the development of innovative, theory-based educational strategies and support the integration of AI-supported and gamified training approaches into healthcare institutions to enhance occupational safety among nurses.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

36

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen
  • Ældre voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Registered nurses working in the participating hospitals
  • Working in the institution for at least 2 months (Phase 1) or newly employed within the last 1 month (Phase 2)
  • Willing to participate in the study
  • Able to use smartphone-based technologies
  • Providing written informed consent

Exclusion Criteria:

  • Having received prior training based on the Health Belief Model for sharps injury prevention
  • Previous professional nursing experience before current employment (for newly recruited nurses in Phase 2)
  • Being on leave during the data collection period
  • Failure to attend training sessions (intervention group)
  • Incomplete data collection forms
  • Withdrawal from the study at any stage

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Forebyggelse
  • Tildeling: Ikke-randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Intervention Group
Nurses in the intervention group will receive a Health Belief Model-based, AI-supported gamified training program designed to improve knowledge and attitudes toward sharps injury prevention.
A structured training program consisting of seven sessions, incorporating artificial intelligence-supported educational content, gamified scenarios, interactive videos, and digital feedback mechanisms to enhance learning and promote behavior change.
Aktiv komparator: Control Group
Standard training provided by the institution, including lectures and question-answer sessions on sharps injury prevention.
Standard training provided by the institution, including lectures and question-answer sessions on sharps injury prevention.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Nurses' knowledge level regarding sharps injury prevention
Tidsramme: Baseline (pretest), immediately after the intervention (posttest), and 2 months after the intervention
Knowledge level will be assessed using a structured knowledge questionnaire consisting of 25 items developed based on the literature. Higher scores indicate greater knowledge regarding sharps injury prevention.
Baseline (pretest), immediately after the intervention (posttest), and 2 months after the intervention

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Attitudes toward safe use of sharps
Tidsramme: Baseline, immediately after the intervention, and 2 months after the intervention
Attitudes will be measured using the "Attitude Scale for Safe Use of Sharps Medical Instruments," a validated Likert-type scale. Higher scores indicate more positive attitudes toward safe practices.
Baseline, immediately after the intervention, and 2 months after the intervention
Sharps injury risk perception and prediction score
Tidsramme: Baseline, immediately after the intervention, and 2 months after the intervention
Risk perception and prediction will be assessed using the adapted Sharps Injury Prediction Scale based on the Health Belief Model. Higher scores reflect increased perceived severity, benefits, and awareness of preventive behaviors.
Baseline, immediately after the intervention, and 2 months after the intervention

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Ziyafet Uğurlu, Professor, Baskent University

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Anslået)

1. juni 2026

Primær færdiggørelse (Anslået)

1. september 2026

Studieafslutning (Anslået)

1. juni 2027

Datoer for studieregistrering

Først indsendt

26. april 2026

Først indsendt, der opfyldte QC-kriterier

26. april 2026

Først opslået (Faktiske)

1. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

1. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

26. april 2026

Sidst verificeret

1. april 2026

Mere information

Begreber relateret til denne undersøgelse

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

IPD-planbeskrivelse

Individual participant data (IPD) will not be shared due to ethical and privacy considerations. The study involves human participants, and sharing individual-level data may pose a risk to confidentiality despite anonymization. Data will be used solely for research purposes in accordance with ethical approval and institutional regulations.

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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Kliniske forsøg med Experimental: Intervention Group

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