- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06925620
Effectiveness of a Multimodal IT Enhanced Hand Hygiene Strategy on Healthcare Associated Infections in Nursing Homes
April 27, 2025 updated by: Kaohsiung Medical University Chung-Ho Memorial Hospital
Effectiveness of Multimodal Information Technology-enhanced Hand Hygiene Improvement Strategy on Healthcare-associated Infections in Nursing Homes
This study aims to evaluate the effectiveness of a multimodal hand hygiene improvement strategy, enhanced with information technology (IT), in reducing healthcare-associated infections (HAIs) in nursing homes.
The goal is to improve infection prevention practices and promote a safer environment for older adults living in long-term care facilities.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Hand hygiene is a key strategy for preventing healthcare-associated infections (HAIs), yet compliance among healthcare workers remains suboptimal due to knowledge gaps, limited resources, unfamiliarity with procedures, and poor adherence.
This study aims to assess the effectiveness of an IT-enhanced multimodal hand hygiene intervention in reducing HAIs within nursing homes, thereby improving infection control practices and promoting a safer environment for older adults in long-term care settings.
Study Type
Interventional
Enrollment (Actual)
91
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Kaohsiung, Taiwan
- Kaohsiung Nursing Home
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Pingtung, Taiwan
- Pingtung Nursing Home
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Full-time nurses or nursing assistants in the participating nursing homes
- Proficiency in Mandarin or Taiwanese
Exclusion Criteria:
• Confirmed or anticipated resignation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental group
received a three-month IT-enhanced program.
|
The intervention, adapted from the WHO's multimodal strategy, incorporated IT-based components to enhance hand hygiene compliance.
A one-time, 1-hour online education session via Google Meet covered the WHO's Five Moments and seven-step handwashing technique, with real-time feedback using fluorescent dye and UV light.
Post-session videos were available on tablets for review.
Visual reminders, such as screensavers and digital posters, reinforced learning.
Smart sanitizer dispensers with seven-step lights and a 20-second countdown were installed at five key sites, RFID-linked to staff badges for automatic tracking.
Monthly performance data were shared via bulletin boards and LINE, with SMS feedback to top and bottom performers.
Daily audio reminders played at 9 a.m. and 5 p.m., and high performers were recognized in monthly meetings.
|
|
No Intervention: Control group
Continued routine care and only took part in the same measurements
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hand hygiene Compliance Rates
Time Frame: 4 month
|
Hand hygiene compliance data were collected using the "Hand Hygiene Compliance Rate and Behavior Inspection Checklist for Long-term Care Facility Workers"(%)
|
4 month
|
|
Hand hygiene Accuracy Rates
Time Frame: 4 month
|
Hand hygiene Accuracy data were collected using the "Hand Hygiene Compliance Rate and Behavior Inspection Checklist for Long-term Care Facility Workers"(%)
|
4 month
|
|
Density of healthcare-associated infections
Time Frame: 4 month
|
A facility's "density of HAI" followed Taiwan's Centers for Disease Control (2012) guidelines(‰)
|
4 month
|
|
Hand Hygiene Knowledge
Time Frame: 1 month
|
Cognitive scores were obtained through a "Hand Hygiene Knowledge Questionnaire for Long-term Care Facility Workers" It comprised 15 items (12 true/false, 2 multiple-choice, 1 multiple-answer), awarding 1 point for each correct answer and 0 for incorrect or unsure response, with a total score ranging from 0 to 15.
Higher scores indicated greater hand hygiene knowledge.
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 17, 2022
Primary Completion (Actual)
December 1, 2022
Study Completion (Actual)
December 1, 2022
Study Registration Dates
First Submitted
April 7, 2025
First Submitted That Met QC Criteria
April 11, 2025
First Posted (Actual)
April 13, 2025
Study Record Updates
Last Update Posted (Actual)
April 30, 2025
Last Update Submitted That Met QC Criteria
April 27, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KMUHIRB-F(I)-20220007
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
for personal privacy reason
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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