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Fluorescent Hand Hygiene Training and Long-Term Effects in First-Year Nursing Students

10. august 2026 opdateret af: Powiślańska Academy of Applied Sciences

Durability of Fluorescent Hand Hygiene Training Effects Among First-Year Nursing Students: A Single-Group Quasi-Experimental Before-After Study With Repeated Measures of Knowledge and Technique

This single-group quasi-experimental study will evaluate the effectiveness and durability of a fluorescent hand hygiene training program for first-year nursing students at a Polish university. Students will complete the WHO Hand Hygiene Knowledge Questionnaire and undergo Glo Germ-based fluorescent assessment of handwashing technique at baseline, immediately after the training, approximately two weeks later, at the end of the first semester, and just before their first clinical placements. The primary objective is to determine whether the training improves and sustains hand hygiene technique quality over time, while secondary objectives include changes in hand hygiene knowledge and the relationship between knowledge and technique

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

80

Fase

  • Ikke anvendelig

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

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • First-year nursing students enrolled at Powiślańska Academy of Applied Sciences in Kwidzyn during the study period.
  • Aged 18 years or older.
  • Able to provide written informed consent.
  • Able to participate in the planned educational activities.

Exclusion Criteria:

  • Known allergy or skin intolerance to Glo Germ™ /gel or similar products.
  • Current dermatological condition of the hands that precludes the use of fluorescent lotion/gel or repeated handwashing (e.g., severe eczema or open wounds).
  • Previous participation in a pilot study or an earlier version of the same fluorescent hand-hygiene training at this institution.

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: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Fluorescent Hand Hygiene Training Arm
First-year nursing students receive a standardized fluorescent hand hygiene training session using Glo Germ lotion and UV light. The session includes a brief review of WHO hand hygiene indications, demonstration of proper handwashing technique, application of fluorescent lotion, handwashing by the student, and visual feedback of missed areas under UV illumination. Students repeat handwashing until adequate coverage is achieved. This training is delivered early in the first semester and its effects are assessed at immediate, short-term, semester-end, and pre-clinical time points

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Quality of hand hygiene technique assessed with fluorescent Glo Germ
Tidsramme: Baseline, immediately post-training, approximately 2 weeks post-training, end of first semester, and just before first clinical placements
Baseline, immediately post-training, approximately 2 weeks post-training, end of first semester, and just before first clinical placements
Quality of hand hygiene technique assessed with fluorescent Glo Germ
Tidsramme: Baseline, immediately post-training, approximately 2 weeks post-training, end of first semester, and just before first clinical placements
Hand hygiene technique will be evaluated at five time points using Glo Germ fluorescent lotion and UV light. After applying fluorescent lotion, students wash their hands as usual; residual fluorescence indicating missed areas is recorded by the investigator on a standardized checklist (e.g., fingertips, thumbs, interdigital spaces, dorsal surfaces). The primary outcome will be the proportion of students achieving adequate technique (no or minimal missed areas) and changes in individual technique scores over time
Baseline, immediately post-training, approximately 2 weeks post-training, end of first semester, and just before first clinical placements

Samarbejdspartnere og efterforskere

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

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)

15. oktober 2026

Primær færdiggørelse (Anslået)

30. juni 2027

Studieafslutning (Anslået)

30. juni 2027

Datoer for studieregistrering

Først indsendt

3. august 2026

Først indsendt, der opfyldte QC-kriterier

10. august 2026

Først opslået (Faktiske)

11. august 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

11. august 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

10. august 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • PANS-HH-EDU-2026
  • 1/2026 (Powiślańska Akademia Nauk Stosowanych w Kwidzynie)

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

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