MedTrace Logo

Education Program of Hand Hygiene for Nursing Students

NCT05872581 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 280

Last updated 2023-09-21

No results posted yet for this study

Summary

The goal of this observational study is to design and test a multicomponent education program of hand hygiene in nursing students. The main aims are:

1. conduct a randomized controlled trial (RCT) to test the effectiveness of this program on knowledge and practice of hand hygiene in nursing students;
2. evaluate the effects of each component and collect feedbacks from participants.

Participants will be randomly assigned into the three intervention: Group A (Hand scanner instant feedback) , Group B (Video training), Group C (Hand scanner + Video training) , and Group D (Control group without intervention). Pre- and post-intervention assessment will be used to evaluate the effectiveness of the program and individual components.

Conditions

  • Hand Hygiene

Interventions

BEHAVIORAL

Hand scanner instant feedback

Participants will be informed about their hand scanner results of the first hand washing attempt to get individualized feedback about their hand wash performance.

BEHAVIORAL

Video training

Participants will watch a training video about the 7 steps of hand washing after the first hand washing attempt.

Sponsors & Collaborators

  • The Hong Kong Polytechnic University

    lead OTHER

Principal Investigators

  • Lin Yang, PhD · The Hong Kong Polytechnic University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-06-01
Primary Completion
2023-07-31
Completion
2023-07-31

Countries

  • Hong Kong

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05872581 on ClinicalTrials.gov