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Effect of Glo Germ Visual Feedback on Surgical Hand Antisepsis in Nursing Students (GLO-SHA)

30. oktober 2026 oppdatert av: Dilek YILDIRIM TANK, Zonguldak Bulent Ecevit University

Beyond Checklists: Glo Germ Feedback Improves Anatomical Surgical Hand Antisepsis

This randomized controlled study evaluated the effect of Glo Germ-based visual feedback on surgical hand antisepsis performance among undergraduate nursing students.

A total of 46 third-year nursing students enrolled in an Operating Room Nursing course were randomly assigned to an intervention group (n=23) or a control group (n=23). Both groups received theoretical instruction and conventional practical training in surgical hand antisepsis. In addition, the intervention group received individualized visual feedback using Glo Germ fluorescent training lotion and ultraviolet light to identify areas requiring improvement in hand antisepsis technique.

The primary outcome was surgical hand antisepsis skill performance. Secondary outcomes included knowledge of surgical hand antisepsis and anatomical hand cleanliness. Outcomes were evaluated at the designated assessment points, including a one-month follow-up.

The study aimed to determine whether incorporating fluorescence-based visual feedback into conventional training improves surgical hand antisepsis education among nursing students.

Studieoversikt

Detaljert beskrivelse

Surgical hand antisepsis is an essential component of infection prevention in perioperative settings. Effective surgical hand antisepsis requires both theoretical knowledge and the correct application of antisepsis procedures, including adequate coverage of anatomical hand and forearm surfaces. Traditional educational methods may not provide sufficient visual information to help students recognize areas missed during hand antisepsis.

This study was designed as a prospective, parallel-group randomized controlled educational trial to evaluate the effectiveness of Glo Germ-based visual feedback in surgical hand antisepsis training among undergraduate nursing students.

The study included 46 third-year nursing students enrolled in an Operating Room Nursing course at a university in Zonguldak, Türkiye. Participants were randomly allocated to an intervention group (n=23) or a control group (n=23) using a computer-generated randomization sequence. Allocation concealment was implemented using sequentially numbered, opaque, sealed envelopes.

Both groups received a 45-minute theoretical educational session and conventional practical instruction on surgical hand antisepsis. Students in the control group received conventional verbal feedback during practical training.

In addition to conventional training, students in the intervention group received Glo Germ-based visual feedback. A fluorescent training lotion and ultraviolet light were used to visualize anatomical areas requiring improvement. Participants received individualized feedback and repeated the hand antisepsis procedure to reinforce correct technique.

The primary outcome was surgical hand antisepsis skill performance, assessed using an 18-item observational checklist. Secondary outcomes included surgical hand antisepsis knowledge, assessed using a 15-item knowledge assessment form, and anatomical hand cleanliness, evaluated through fluorescence-based visual assessment.

Knowledge was assessed at baseline, immediately after training, and at the one-month follow-up. Skill performance was assessed immediately after training and at the one-month follow-up. Fluorescence-based anatomical cleanliness assessment was conducted at the assessment points specified in the study protocol.

Outcome assessments were performed by independent assessors who were blinded to group allocation. The study investigated whether adding individualized fluorescence-based visual feedback to conventional surgical hand antisepsis education improves students' knowledge, practical skills, and anatomical cleanliness.

Studietype

Intervensjonell

Registrering (Faktiske)

46

Fase

  • Ikke aktuelt

Kontakter og plasseringer

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

Studiesteder

      • Zonguldak, Tyrkia (Türkiye), 67600
        • Zonguldak Bülent Ecevit University

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

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

Being a third-year undergraduate nursing student enrolled in the Operating Room Nursing course.

Voluntarily agreeing to participate in the study. Providing written informed consent.

Exclusion Criteria:

Having open wounds, cuts, or skin lesions on the hands that could interfere with surgical hand antisepsis procedures.

Having hand eczema or other dermatological conditions affecting the hands that could interfere with training or assessment.

Declining to participate in the study.

Studieplan

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

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Annen
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Glo Germ Visual Feedback Group

Participants received a 45-minute theoretical session and conventional practical training on surgical hand antisepsis. In addition, they received individualized visual feedback using Glo Germ fluorescent training lotion and ultraviolet light to identify areas requiring improvement in hand antisepsis technique. Participants repeated the procedure following visual feedback.

An educational intervention incorporating Glo Germ fluorescent training lotion and ultraviolet light to provide individualized visual feedback during surgical hand antisepsis training. The intervention enabled participants to identify anatomical areas requiring improvement and repeat the antisepsis procedure following feedback.

Aktiv komparator: Conventional Training Group

Participants received a 45-minute theoretical session and conventional practical training on surgical hand antisepsis. Conventional verbal feedback was provided during practical training. Participants did not receive Glo Germ-based visual feedback.

Participants received a 45-minute theoretical educational session covering the principles, importance, and correct procedures of surgical hand antisepsis. This was followed by conventional practical training, including demonstration and supervised practice of surgical hand antisepsis techniques. Verbal feedback was provided to support correct technique and improve participants' practical skills. This standard educational intervention was provided to both the experimental and control groups.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Surgical Hand Antisepsis Skill Performance
Tidsramme: Immediately after training and at 1-month follow-up

Surgical hand antisepsis skill performance was assessed using an 18-item observational checklist evaluating the correct execution of surgical hand antisepsis procedures. Each correctly performed step was scored as 1, and each incorrectly performed or omitted step was scored as 0. Total scores ranged from 0 to 18, with higher scores indicating better surgical hand antisepsis performance. Assessments were conducted immediately after training and at the one-month follow-up.

Immediately after training and at 1-month follow-up

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Surgical Hand Antisepsis Knowledge
Tidsramme: Baseline, immediately after training, and at 1-month follow-up

Knowledge of surgical hand antisepsis was assessed using a 15-item knowledge assessment form. Total scores ranged from 0 to 15, with higher scores indicating greater knowledge of surgical hand antisepsis. Knowledge was assessed at baseline, immediately after training, and at the one-month follow-up.

Baseline, immediately after training, and at 1-month follow-up
Percentage of Anatomical Hand Cleanliness
Tidsramme: Immediately after training (intervention group only) and at 1-month follow-up (both groups)

Anatomical hand cleanliness was assessed using Glo Germ fluorescent training lotion and ultraviolet light. The anatomical regions of the hands and forearms were examined to identify areas with inadequate coverage during surgical hand antisepsis training. The assessment results were calculated and expressed as percentages. Higher percentages indicated better anatomical hand cleanliness. Assessments were performed immediately after training in the intervention group and at the one-month follow-up in both groups.

Immediately after training (intervention group only) and at 1-month follow-up (both groups)

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Publikasjoner og nyttige lenker

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Generelle publikasjoner

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 (Faktiske)

30. november 2024

Primær fullføring (Faktiske)

30. desember 2024

Studiet fullført (Faktiske)

30. desember 2024

Datoer for studieregistrering

Først innsendt

30. oktober 2026

Først innsendt som oppfylte QC-kriteriene

30. oktober 2026

Først lagt ut (Faktiske)

5. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

5. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

30. oktober 2026

Sist bekreftet

1. oktober 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 will not be made publicly available. The study data will be maintained confidentially and used in accordance with the approved research protocol, institutional policies, and applicable data protection regulations.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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