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

30 de octubre de 2026 actualizado por: 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.

Descripción general del estudio

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Actual)

46

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

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.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Otro
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Único

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.

Comparador activo: 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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Surgical Hand Antisepsis Skill Performance
Periodo de tiempo: 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

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Surgical Hand Antisepsis Knowledge
Periodo de tiempo: 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
Periodo de tiempo: 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)

Colaboradores e Investigadores

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Publicaciones y enlaces útiles

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Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

30 de noviembre de 2024

Finalización primaria (Actual)

30 de diciembre de 2024

Finalización del estudio (Actual)

30 de diciembre de 2024

Fechas de registro del estudio

Enviado por primera vez

30 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

30 de octubre de 2026

Publicado por primera vez (Actual)

5 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

5 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

30 de octubre de 2026

Última verificación

1 de octubre de 2026

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • GLOGERM SURGİCAL HAND WASHING

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Descripción del plan IPD

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.

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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