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AI-Supported Gamified Training for Sharps Injury Prevention in Nurses

26. april 2026 oppdatert av: 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.

Studieoversikt

Detaljert 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.

Studietype

Intervensjonell

Registrering (Antatt)

36

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
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
Tiltaksbeskrivelse
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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Ziyafet Uğurlu, Professor, Baskent University

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. juni 2026

Primær fullføring (Antatt)

1. september 2026

Studiet fullført (Antatt)

1. juni 2027

Datoer for studieregistrering

Først innsendt

26. april 2026

Først innsendt som oppfylte QC-kriteriene

26. april 2026

Først lagt ut (Faktiske)

1. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

1. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

26. april 2026

Sist bekreftet

1. april 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

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.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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