Hand Hygiene TrainingHANDHEARTNCT07280026
Effectiveness of an Edge AI-based Augmented Reality System for Hand Hygiene Training: a Multi-centre, Mixed-methods Cluster Randomised Controlled Trial
A study testing Instructional Video + Scanner Feedback and Edge AI-based AR Hand Hygiene Training System in people with Hand Hygiene Training and Infection Prevention and Control, run by The Hong Kong Polytechnic University at 3 sites in 2 countries.
Trial summary
This multi-centre, mixed-methods cluster randomised controlled trial (cRCT) aims to evaluate the effectiveness of an edge artificial intelligence (AI)-based augmented reality (AR) training and assessment system for improving hand hygiene knowledge and practice across healthcare and educational settings. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Hand Hygiene Training, Infection Prevention and Control, Healthcare-Associated Infections (HAIs)
- What is being tested?
- Instructional Video + Scanner Feedback and Edge AI-based AR Hand Hygiene Training System
- Type of treatment
- Medical device, Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1,000 participants
- Where
- 3 sitesin 2 countries
- Study dates
- 15 Dec 2025to 1 Sep 2027
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Undergraduate students enrolled in health-related disciplines (e.g., nursing, medicine, rehabilitation sciences, medical laboratory science) at participating universities
- Healthcare professionals or supporting staff working in participating hospitals
- Able to provide informed consent
- Willing to participate in both pre- and post-training assessments during the same study visit
- Aged 18 years or above
Who cannot join
- Known allergy or skin irritation to fluorescent powder or hand hygiene products
- Current visible skin conditions (e.g., dermatitis, eczema, open wounds) on hands that may interfere with handwashing assessment
- Unable to understand or follow the training instructions
- Refusal or inability to provide written informed consent
Trial locations and contacts
3 sites in 2 countries. Contact the study team or a site near you to ask about taking part.
3 sites in 2 countries
Hong Kong2 sites, 2 recruiting
- Recruiting
The Hong Kong Polytechnic University
Hung Hom, Hong Kong
Lin Yang, Doctor, +852 2766 6398, l.yang@polyu.edu.hk
- Not yet recruiting
The Chinese University of Hong Kong
Shatin, Hong Kong
Christopher K C Lai, Doctor, 852-35051523, chris.kclai@cuhk.edu.hk
China1 site, 1 recruiting
- Not yet recruiting
Tongji Hospital
Wuhan, Hubei
Lin Yang, Doctor, +852 2766 6398, l.yang@polyu.edu.hk
About this study
This multi-centre, mixed-methods cluster randomised controlled trial (cRCT) aims to evaluate the effectiveness of an edge artificial intelligence (AI)-based augmented reality (AR) training and assessment system for improving hand hygiene knowledge and practice across healthcare and educational settings. Hand hygiene remains one of the most effective measures to prevent healthcare-associated infections (HAIs), which cause substantial morbidity, mortality, and economic burden worldwide. Despite ongoing education efforts, conventional training methods-such as lectures and standard videos-often lack individualised feedback and interactivity, limiting behavioural improvement. The proposed AI-empowered AR system provides real-time assessment and personalised guidance, potentially transforming hand hygiene education into an adaptive, scalable, and evidence-driven learning experience.
The trial will be conducted at three centres: the Hong Kong Polytechnic University and the Chinese University of Hong Kong in Hong Kong SAR, and Tongji Hospital in Wuhan, China. Approximately 480 participants will be enrolled, including 240 undergraduate students in health-related disciplines and 240 healthcare professionals or supporting staff from hospitals. Cluster randomisation will be applied at the session level (6-25 participants per cluster). Randomisation will be performed by a statistician independent from recruitment, and allocation concealment will be maintained. The study will adopt a non-inferiority design, comparing the AI-based AR system against an existing validated educational program combining hand scanner feedback and instructional videos. Participants and assessors of handwashing quality will remain blinded to group allocation.
Read more
At baseline, participants will provide written informed consent and complete a standardized questionnaire assessing hand hygiene knowledge and practice. They will apply fluorescent powder to both hands and perform an initial handwashing attempt, recorded by an overhead camera. The percentage of fluorescent residue (measured by the Semmelweis Scanner™) will serve as an objective indicator of decontamination effectiveness, while trained infection prevention and control (IPC) experts will independently assess technique quality from anonymized video recordings. These evaluations will also be used as reference data for AI algorithm development.
In the intervention arm, participants will perform AI-based AR training sessions providing individualized feedback on handwashing performance. In the control arm, participants will receive feedback from the fluorescent scanner and watch a standard "seven-step" handwashing educational video. Following training, participants will repeat the handwashing procedure and post-intervention assessments, including fluorescent residue measurement and the same knowledge-practice questionnaire. The primary outcome is the improvement in decontamination effectiveness (reduction in fluorescent residue percentage between pre- and post-intervention). Secondary outcomes include correct performance of all seven handwashing steps, improvement in knowledge scores, and user satisfaction.
A qualitative component will complement the RCT to explore participants' experiences, attitudes, and perceived barriers toward AI-based AR hand hygiene training. A purposive subsample from both arms will be invited to participate in semi-structured interviews based on the Theoretical Domains Framework. Interviews will examine usability, motivation, learning experience, and perceived behavioral changes. Data will be audio-recorded, transcribed verbatim, and analyzed using thematic analysis with iterative coding to ensure credibility and consistency.
Ethical approval will be obtained from relevant institutional review boards. All participants will be informed of their rights, including voluntary participation and the ability to withdraw at any time without penalty. Potential risks are minimal, limited mainly to rare allergic reactions to fluorescent powder. All data, including video and image recordings, will be anonymised, stored securely, and deleted one year after project completion. No personally identifiable information will be collected.
This study will generate high-quality evidence on the feasibility and educational impact of integrating AI and AR technologies into hand hygiene training across academic and clinical settings. If proven effective, the system can be incorporated into health professional curricula and used at the point of care for real-time performance monitoring and auditing, contributing to sustainable infection prevention and control capacity building.
Read the detailed description
The importance of hand hygiene cannot be underestimated in both healthcare and community settings (Allegranzi et al., 2011; Mathur, 2011). The promotion of hand hygiene is the best practice in preventing health care-associated infection (WHO, 2009). It has been estimated that hand hygiene could reduce over 500 000 attributable deaths per year. It was found that the annual economic impact of health care-associated infection in the US was approximately US$6.5 billion in 2004 (WHO, 2009) and every US$1 spent on hand hygiene promotion could result in a US$23.7 benefit (Chen et al., 2011). Education plays a key role in setting a good practice base in hand hygiene.
The traditional training methods for hand hygiene include in-class lecture and practical, but they seldom receive individualised instructions and feedback due to limited manpower and facilities. Hence, there is an urgent need to design an automated and individualised training system. This proposed project aims to design and test an innovative education tool for hand hygiene, with the following specific objectives:
- develop a prototype of the AI-empowered AR system for hand hygiene training and assessment;
- conduct a multi-centre, mixed-methods non-inferiority randomised controlled trial (RCT) to test the effectiveness of this AI-based AR training system on knowledge and practice of hand hygiene in in in different populations in different settings, including undergraduate students of health-related disciplines, healthcare professionals and supporting staff in hospitals;
- evaluate the effects of the AI-based AR training system and collect feedback from participants.
- investigate participants' experiences, attitudes, and perceptions of hand hygiene training using user feedback survey and focus group interviews.
If demonstrated effective, this system can be integrated into the curriculum of students of health-related disciplines, healthcare professionals and supporting staff from hospitals as an e-learning approach. In future, this system can also be used at point-of-care for real-time monitoring and audit of healthcare workers in other healthcare settings. In addition to quantitative outcome measures, qualitative interviews will be conducted to explore students' learning experiences, attitudes, and perceived barriers regarding hand hygiene practice and the use of AI-based AR training tools.
Methods
Study design This is a mixed-methods study consisting of a multi-centre non-inferiority two-arm randomised controlled trial (RCT) and a qualitative component. The RCT will evaluate the effectiveness of the AI-based AR training system on students' knowledge and practice of hand hygiene, while the qualitative study will explore students' experiences, attitudes, and perceived barriers related to hand hygiene training through semi-structured interviews. There are three centres for this trial: the Hong Kong Polytechnic University, Chinese University of Hong Kong, and Tongji Hospital in Wuhan, China. We will recruit eligible undergraduates from two universities, and healthcare professionals/supporting staff from Tongji Hospital.
Subject recruitment We will recruit 480 undergraduate students from health-related disciplines from the Hong Kong Polytechnic University, and the Chinese University of Hong Kong (n=240); healthcare professionals and supporting staff in hospitals (n=240). Data collection will be conducted during September 2025 to December 2026. Participants will subscribe a time slot of training sessions (each session has up to 25 participants). All participants who attend the same session will be assigned to the same group by cluster randomisation. A statistician will assign the groups in advance by a random number generator. The participants will not be informed about their group before arriving the study sites.
We calculated the sample size for a cluster randomised controlled trial. We assume that the number of participants in each cluster ranges from 6 to 25, there will be approximately 10-30 clusters in each group. We also assume the standard deviation of subjects is 2.00, the intracluster correlation coefficient is 0.010, and the coefficient of variation of cluster sizes is 0.500 (Ahn et al. 2015). The total sample size of 480 can achieve >91% power to detect a difference between two group means (confidence interval -1.0 and 1.0) in a two-sided t-test with a significance level of 0.050.
Pre-intervention assessment During the site visit, the participants will be invited to sign a consent form first and fill in a questionnaire on knowledge and practice of hand hygiene (attached in Appendix 1).
Participants will need to put fluorescent powder on both of their hands and then perform hand washing using liquid soap without any instructions (1st HW attempt). The camera installed above the hand-wash basins will take videos of both hands (no face nor other parts of the body) during this procedure. After washing hands, participants will need to scan fluorescent powder remained on their hands in a hand scanner (The Semmelweis Scanner™). The recorded hand washing videos will be used to train the AI algorithms for automatic image processing and assessments. Two IPC experts will judge the quality of hand hygiene in these videos, which will be adopted as ground truth in image processing. The percentage of fluorescent gel residual on hands shown in the hand scanner will be used as an objective assessment for efficacy of hand washing in individual participants.
Interventions groups Group A (AI-based AR training system) Participants will use the AI-empowered AR training system to get individualised assessments of their hand wash performance. They will not be informed about the hand scanner results.
Group B (Hand scanner + Video training) Participants will use an existing education program that has been demonstrated effective in our previous study (unpublished). In brief, the participants will be informed about their hand scanner results during the first HW attempt. They will also watch a training video about the 7 steps of hand washing.
Post-intervention assessment The participants will take the second HW attempt by putting fluorescent powder on both of their hands again and then perform hand wash with videos recorded. After washing hands, participants will scan fluorescent powder remained on their hands again in a hand scanner.
Participants will also be asked to fill in a questionnaire on knowledge and practice of hand hygiene as part of post-intervention assessment.
Qualitative Study In addition to the randomised controlled trial, a qualitative component will be conducted to explore participants' experiences, attitudes, and perceived barriers toward hand hygiene training (see Appendix 2). A purposive subsample of participants from both intervention and control groups will be invited to join semi-structured interviews guided by the Theoretical Domains Framework (Cane et al., 2012). The interviews will cover topics such as learning experience, motivation, usability, knowledge, skills, and social influences. All interviews will be audio-recorded and transcribed verbatim. Data will be analysed using thematic analysis, with initial codes generated inductively and then organised into broader categories and themes. Themes will be iteratively reviewed and refined to ensure credibility and consistency. Written informed consent will be obtained prior to participation, and confidentiality and voluntary participation will be strictly observed. Each participant will get a 100 HKD coupon. The sample coupon signature form can be found in Appendix 3.
Randomisation, allocation concealment, and blinding Participants will be randomly assigned to the intervention groups through a process of randomisation performed by a statistician who will not be involved in subject recruitment. The participants will be blinded. The RAs involved in subject recruitment and the IPC experts who judge the quality of hand hygiene will be blinded to the groupings. The RAs and student assistants involved in hand hygiene video recording at the study site will not be blinded because they will be giving instructions to the participants.
Ethical consideration
It is anticipated that the education program will not pose any physical or psychological harm to the participants. There is a very low chance of skin allergy to fluorescent powder. If a participant shows any sign of skin allergy, she or he will instantly stop the trail. The contact details of either the ethical or the research in-charge personnel are clearly written in the information sheet.
Explanation of the study will be given to participants who are interested in participating in the study. Participants will also be given the opportunity to ask our project personnel questions. Furthermore, the information sheet including the purpose of the study, confidentiality of the data, and rights of the participants, will also be provided to the participants. The contact details of either the ethical or the research in-charge personnel are clearly written in the information sheet. If they agree to participate in the study, they are required to sign the consent form. Their participation is on a voluntary basis; they have the right to withdraw from the study at any time if they want to without consequence.
All the collected data will be kept confidentially, and only the research personnel can access and handle the data. No personal information of the participants will be collected except the student ID number. For the qualitative component, participants will also be asked for consent to participate in interviews. All interview data will be anonymised and handled confidentially.
Confidentiality and Security
Data collection will be anonymous, only analysed for specified purposes and based on the consent or other legitimate basis laid down by law. No personal information will be linked to image/video data. All the image/video data will be deleted one year after the project is completed. The Project will not involve any activities or results raising security issues.
References
Allegranzi, B., Bagheri Nejad, S., Combescure, C., Graafmans, W., Attar, H., Donaldson, L., \& Pittet, D. (2011). Burden of endemic health-care-associated infection in developing countries: systematic review and meta-analysis. Lancet, 377(9761), 228-241. https://doi.org/10.1016/S0140-6736(10)61458-4
Ahn, C., Heo, M., \& Zhang, S. (2015). Sample Size Calculations for Clustered and Longitudinal Outcomes in Clinical Research. CRC Press. New York.
Chen, Y. C., Sheng, W. H., Wang, J. T., Chang, S. C., Lin, H. C., Tien, K. L., Hsu, L. Y., \& Tsai, K. S. (2011). Effectiveness and limitations of hand hygiene promotion on decreasing healthcare-associated infections. PLoS One, 6(11), e27163. https://doi.org/10.1371/journal.pone.0027163
Mathur, P. (2011). Hand hygiene: back to the basics of infection control. Indian J Med Res, 134(5), 611-620. https://doi.org/10.4103/0971-5916.90985
WHO. (2009). In WHO Guidelines on Hand Hygiene in Health Care: First Global Patient Safety Challenge Clean Care Is Safer Care. https://www.ncbi.nlm.nih.gov/pubmed/23805438
Yang, L., Lu, Y., Cao, J., Huang, J., \& Zhang, M. (2020). E-Tree Learning: A Novel Decentralized Model Learning Framework for Edge AI. IEEE Internet of Things Journal.
Cane, J., O'Connor, D., \& Michie, S. (2012). Validation of the theoretical domains framework for use in behaviour change and implementation research. Implementation science, 7(1), 37.
- Conditions
- Hand Hygiene Training, Infection Prevention and Control, Healthcare-Associated Infections (HAIs), Health Education
- Being tested
- Instructional Video + Scanner Feedback, Edge AI-based AR Hand Hygiene Training System
- Keywords
- hand hygiene, health education, infection prevention and control
- Medical subject headings
- Cross Infection, Health Education
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Instructional Video + Scanner FeedbackBehavioural
Viewing quantified fluorescent residue from the first handwash plus a standard 7-step instructional video prior to the second handwash.
Edge AI-based AR Hand Hygiene Training SystemDevice
An edge AI + AR system using computer vision to assess handwashing performance and deliver real-time, individualized guidance before the second handwash.
| Study group | Role | What they receive |
|---|---|---|
| Scanner Feedback + Instructional Video | Active comparator | All participants first perform a baseline handwash with fluorescent powder (no guidance). In this arm, participants view their baseline fluorescent residue results (Semmelweis Scanner™) and then watch a standard 7-step instructional video. They immediately perform a second handwash (post-training). Outcomes include change in fluorescent residue (%) and technique quality. Receives: Behavioral: Instructional Video + Scanner Feedback |
| Edge AI-based AR Hand Hygiene Training | Experimental | All participants first perform a baseline handwash with fluorescent powder (no guidance). In this arm, participants do not view their baseline fluorescent residue. They proceed directly to AI-based AR training that provides real-time individualized feedback on the 7-step technique, then immediately perform a second handwash (post-training). Outcomes include change in fluorescent residue (%) and technique quality. Receives: Device: Edge AI-based AR Hand Hygiene Training System |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in decontamination effectiveness (percentage of fluorescent residue on both hands)
The main outcome assesses the effectiveness of hand hygiene training by measuring the change in residual fluorescent powder percentage between the first (pre-training) and second (post-training) handwashing attempts. Fluorescent residue will be quantified using the Semmelweis Scanner™ to objectively evaluate handwashing effectiveness.
Measured: Immediately after intervention (within the same study visit)
Secondary outcomes (1)
Change in hand hygiene knowledge and self-reported practice scores
Knowledge and self-reported practice of hand hygiene will be assessed using a standardized questionnaire administered before and after training. Scores will be compared to determine the change attributable to each intervention.
Measured: Immediately after intervention (within the same study visit)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Dec 2025
- Study start15 Dec 2025 (estimated)
- Primary completion1 Aug 2027 (estimated)
- Study completion1 Sep 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (4)Papers the sponsor has linked to this study.
- Other trials for Hand Hygiene TrainingStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 1,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- The Hong Kong Polytechnic University
- Sponsor type
- University, hospital or other
- Collaborators
- Chinese University of Hong Kong, Tongji Hospital
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07280026
- Sponsor's protocol ID
- HSEARS20250907003
- Acronym
- HANDHEART
- Status last verified
- Nov 2025
- First submitted
- 1 Dec 2025
- Last updated
- 12 Dec 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Publications
Cane J, O'Connor D, Michie S. Validation of the theoretical domains framework for use in behaviour change and implementation research. Implement Sci. 2012 Apr 24;7:37. doi: 10.1186/1748-5908-7-37.
PubMed 22530986Chen YC, Sheng WH, Wang JT, Chang SC, Lin HC, Tien KL, Hsu LY, Tsai KS. Effectiveness and limitations of hand hygiene promotion on decreasing healthcare-associated infections. PLoS One. 2011;6(11):e27163. doi: 10.1371/journal.pone.0027163. Epub 2011 Nov 16.
PubMed 22110610Shin J, Kang EM, Lee SH, Heo M, Lee YJ, Lee SJ, Hong SJ, Kim JS, Kim BK, Ko YG, Choi D, Hong MK, Jang Y, Ahn CM. Prognostic implication of venoarterial extracorporeal membrane oxygenation in acute myocardial infarction-related cardiogenic shock. J Intensive Care. 2025 Jul 2;13(1):38. doi: 10.1186/s40560-025-00807-w.
PubMed 40605095Allegranzi B, Bagheri Nejad S, Combescure C, Graafmans W, Attar H, Donaldson L, Pittet D. Burden of endemic health-care-associated infection in developing countries: systematic review and meta-analysis. Lancet. 2011 Jan 15;377(9761):228-41. doi: 10.1016/S0140-6736(10)61458-4. Epub 2010 Dec 9.
PubMed 21146207
Study at a glance
From the registry record, last updated by the sponsor on 12 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effectiveness of an Edge AI-based Augmented Reality System for Hand Hygiene Training: a Multi-centre, Mixed-methods Cluster Randomised Controlled Trial
- ClinicalTrials.gov ID
- NCT07280026
- Acronym / sponsor ID
- HANDHEART / HSEARS20250907003
- Conditions
- Hand Hygiene Training, Infection Prevention and Control, Healthcare-Associated Infections (HAIs), Health Education
- Keywords
- hand hygiene, health education, infection prevention and control
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 1,000 participants (estimated)
- Lead sponsor
- The Hong Kong Polytechnic UniversityUniversity, hospital or other
- Collaborators
- Chinese University of Hong Kong, Tongji Hospital
- Study start
- 15 Dec 2025 (estimated)
- Primary completion
- 1 Aug 2027 (estimated)
- Study completion
- 1 Sep 2027 (estimated)
- First posted
- 12 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This multi-centre, mixed-methods cluster randomised controlled trial (cRCT) aims to evaluate the effectiveness of an edge artificial intelligence (AI)-based augmented reality (AR) training and assessment system for improving hand hygiene knowledge and practice across healthcare and educational settings. Hand hygiene remains one of the most effective measures to prevent healthcare-associated infections (HAIs), which cause substantial morbidity, mortality, and economic burden worldwide. Despite ongoing education efforts, conventional training methods-such as lectures and standard videos-often lack individualised feedback and interactivity, limiting behavioural improvement. The proposed AI-empowered AR system provides real-time assessment and personalised guidance, potentially transforming hand hygiene education into an adaptive, scalable, and evidence-driven learning experience.
The trial will be conducted at three centres: the Hong Kong Polytechnic University and the Chinese University of Hong Kong in Hong Kong SAR, and Tongji Hospital in Wuhan, China. Approximately 480 participants will be enrolled, including 240 undergraduate students in health-related disciplines and 240 healthcare professionals or supporting staff from hospitals. Cluster randomisation will be applied at the session level (6-25 participants per cluster). Randomisation will be performed by a statistician independent from recruitment, and allocation concealment will be maintained. The study will adopt a non-inferiority design, comparing the AI-based AR system against an existing validated educational program combining hand scanner feedback and instructional videos. Participants and assessors of handwashing quality will remain blinded to group allocation.
At baseline, participants will provide written informed consent and complete a standardized questionnaire assessing hand hygiene knowledge and practice. They will apply fluorescent powder to both hands and perform an initial handwashing attempt, recorded by an overhead camera. The percentage of fluorescent residue (measured by the Semmelweis Scanner™) will serve as an objective indicator of decontamination effectiveness, while trained infection prevention and control (IPC) experts will independently assess technique quality from anonymized video recordings. These evaluations will also be used as reference data for AI algorithm development.
In the intervention arm, participants will perform AI-based AR training sessions providing individualized feedback on handwashing performance. In the control arm, participants will receive feedback from the fluorescent scanner and watch a standard "seven-step" handwashing educational video. Following training, participants will repeat the handwashing procedure and post-intervention assessments, including fluorescent residue measurement and the same knowledge-practice questionnaire. The primary outcome is the improvement in decontamination effectiveness (reduction in fluorescent residue percentage between pre- and post-intervention). Secondary outcomes include correct performance of all seven handwashing steps, improvement in knowledge scores, and user satisfaction.
A qualitative component will complement the RCT to explore participants' experiences, attitudes, and perceived barriers toward AI-based AR hand hygiene training. A purposive subsample from both arms will be invited to participate in semi-structured interviews based on the Theoretical Domains Framework. Interviews will examine usability, motivation, learning experience, and perceived behavioral changes. Data will be audio-recorded, transcribed verbatim, and analyzed using thematic analysis with iterative coding to ensure credibility and consistency.
Ethical approval will be obtained from relevant institutional review boards. All participants will be informed of their rights, including voluntary participation and the ability to withdraw at any time without penalty. Potential risks are minimal, limited mainly to rare allergic reactions to fluorescent powder. All data, including video and image recordings, will be anonymised, stored securely, and deleted one year after project completion. No personally identifiable information will be collected.
This study will generate high-quality evidence on the feasibility and educational impact of integrating AI and AR technologies into hand hygiene training across academic and clinical settings. If proven effective, the system can be incorporated into health professional curricula and used at the point of care for real-time performance monitoring and auditing, contributing to sustainable infection prevention and control capacity building.
Detailed description
The importance of hand hygiene cannot be underestimated in both healthcare and community settings (Allegranzi et al., 2011; Mathur, 2011). The promotion of hand hygiene is the best practice in preventing health care-associated infection (WHO, 2009). It has been estimated that hand hygiene could reduce over 500 000 attributable deaths per year. It was found that the annual economic impact of health care-associated infection in the US was approximately US$6.5 billion in 2004 (WHO, 2009) and every US$1 spent on hand hygiene promotion could result in a US$23.7 benefit (Chen et al., 2011). Education plays a key role in setting a good practice base in hand hygiene.
The traditional training methods for hand hygiene include in-class lecture and practical, but they seldom receive individualised instructions and feedback due to limited manpower and facilities. Hence, there is an urgent need to design an automated and individualised training system. This proposed project aims to design and test an innovative education tool for hand hygiene, with the following specific objectives:
- develop a prototype of the AI-empowered AR system for hand hygiene training and assessment;
- conduct a multi-centre, mixed-methods non-inferiority randomised controlled trial (RCT) to test the effectiveness of this AI-based AR training system on knowledge and practice of hand hygiene in in in different populations in different settings, including undergraduate students of health-related disciplines, healthcare professionals and supporting staff in hospitals;
- evaluate the effects of the AI-based AR training system and collect feedback from participants.
- investigate participants' experiences, attitudes, and perceptions of hand hygiene training using user feedback survey and focus group interviews.
If demonstrated effective, this system can be integrated into the curriculum of students of health-related disciplines, healthcare professionals and supporting staff from hospitals as an e-learning approach. In future, this system can also be used at point-of-care for real-time monitoring and audit of healthcare workers in other healthcare settings. In addition to quantitative outcome measures, qualitative interviews will be conducted to explore students' learning experiences, attitudes, and perceived barriers regarding hand hygiene practice and the use of AI-based AR training tools.
Methods
Study design This is a mixed-methods study consisting of a multi-centre non-inferiority two-arm randomised controlled trial (RCT) and a qualitative component. The RCT will evaluate the effectiveness of the AI-based AR training system on students' knowledge and practice of hand hygiene, while the qualitative study will explore students' experiences, attitudes, and perceived barriers related to hand hygiene training through semi-structured interviews. There are three centres for this trial: the Hong Kong Polytechnic University, Chinese University of Hong Kong, and Tongji Hospital in Wuhan, China. We will recruit eligible undergraduates from two universities, and healthcare professionals/supporting staff from Tongji Hospital.
Subject recruitment We will recruit 480 undergraduate students from health-related disciplines from the Hong Kong Polytechnic University, and the Chinese University of Hong Kong (n=240); healthcare professionals and supporting staff in hospitals (n=240). Data collection will be conducted during September 2025 to December 2026. Participants will subscribe a time slot of training sessions (each session has up to 25 participants). All participants who attend the same session will be assigned to the same group by cluster randomisation. A statistician will assign the groups in advance by a random number generator. The participants will not be informed about their group before arriving the study sites.
We calculated the sample size for a cluster randomised controlled trial. We assume that the number of participants in each cluster ranges from 6 to 25, there will be approximately 10-30 clusters in each group. We also assume the standard deviation of subjects is 2.00, the intracluster correlation coefficient is 0.010, and the coefficient of variation of cluster sizes is 0.500 (Ahn et al. 2015). The total sample size of 480 can achieve >91% power to detect a difference between two group means (confidence interval -1.0 and 1.0) in a two-sided t-test with a significance level of 0.050.
Pre-intervention assessment During the site visit, the participants will be invited to sign a consent form first and fill in a questionnaire on knowledge and practice of hand hygiene (attached in Appendix 1).
Participants will need to put fluorescent powder on both of their hands and then perform hand washing using liquid soap without any instructions (1st HW attempt). The camera installed above the hand-wash basins will take videos of both hands (no face nor other parts of the body) during this procedure. After washing hands, participants will need to scan fluorescent powder remained on their hands in a hand scanner (The Semmelweis Scanner™). The recorded hand washing videos will be used to train the AI algorithms for automatic image processing and assessments. Two IPC experts will judge the quality of hand hygiene in these videos, which will be adopted as ground truth in image processing. The percentage of fluorescent gel residual on hands shown in the hand scanner will be used as an objective assessment for efficacy of hand washing in individual participants.
Interventions groups Group A (AI-based AR training system) Participants will use the AI-empowered AR training system to get individualised assessments of their hand wash performance. They will not be informed about the hand scanner results.
Group B (Hand scanner + Video training) Participants will use an existing education program that has been demonstrated effective in our previous study (unpublished). In brief, the participants will be informed about their hand scanner results during the first HW attempt. They will also watch a training video about the 7 steps of hand washing.
Post-intervention assessment The participants will take the second HW attempt by putting fluorescent powder on both of their hands again and then perform hand wash with videos recorded. After washing hands, participants will scan fluorescent powder remained on their hands again in a hand scanner.
Participants will also be asked to fill in a questionnaire on knowledge and practice of hand hygiene as part of post-intervention assessment.
Qualitative Study In addition to the randomised controlled trial, a qualitative component will be conducted to explore participants' experiences, attitudes, and perceived barriers toward hand hygiene training (see Appendix 2). A purposive subsample of participants from both intervention and control groups will be invited to join semi-structured interviews guided by the Theoretical Domains Framework (Cane et al., 2012). The interviews will cover topics such as learning experience, motivation, usability, knowledge, skills, and social influences. All interviews will be audio-recorded and transcribed verbatim. Data will be analysed using thematic analysis, with initial codes generated inductively and then organised into broader categories and themes. Themes will be iteratively reviewed and refined to ensure credibility and consistency. Written informed consent will be obtained prior to participation, and confidentiality and voluntary participation will be strictly observed. Each participant will get a 100 HKD coupon. The sample coupon signature form can be found in Appendix 3.
Randomisation, allocation concealment, and blinding Participants will be randomly assigned to the intervention groups through a process of randomisation performed by a statistician who will not be involved in subject recruitment. The participants will be blinded. The RAs involved in subject recruitment and the IPC experts who judge the quality of hand hygiene will be blinded to the groupings. The RAs and student assistants involved in hand hygiene video recording at the study site will not be blinded because they will be giving instructions to the participants.
Ethical consideration
It is anticipated that the education program will not pose any physical or psychological harm to the participants. There is a very low chance of skin allergy to fluorescent powder. If a participant shows any sign of skin allergy, she or he will instantly stop the trail. The contact details of either the ethical or the research in-charge personnel are clearly written in the information sheet.
Explanation of the study will be given to participants who are interested in participating in the study. Participants will also be given the opportunity to ask our project personnel questions. Furthermore, the information sheet including the purpose of the study, confidentiality of the data, and rights of the participants, will also be provided to the participants. The contact details of either the ethical or the research in-charge personnel are clearly written in the information sheet. If they agree to participate in the study, they are required to sign the consent form. Their participation is on a voluntary basis; they have the right to withdraw from the study at any time if they want to without consequence.
All the collected data will be kept confidentially, and only the research personnel can access and handle the data. No personal information of the participants will be collected except the student ID number. For the qualitative component, participants will also be asked for consent to participate in interviews. All interview data will be anonymised and handled confidentially.
Confidentiality and Security
Data collection will be anonymous, only analysed for specified purposes and based on the consent or other legitimate basis laid down by law. No personal information will be linked to image/video data. All the image/video data will be deleted one year after the project is completed. The Project will not involve any activities or results raising security issues.
References
Allegranzi, B., Bagheri Nejad, S., Combescure, C., Graafmans, W., Attar, H., Donaldson, L., \& Pittet, D. (2011). Burden of endemic health-care-associated infection in developing countries: systematic review and meta-analysis. Lancet, 377(9761), 228-241. https://doi.org/10.1016/S0140-6736(10)61458-4
Ahn, C., Heo, M., \& Zhang, S. (2015). Sample Size Calculations for Clustered and Longitudinal Outcomes in Clinical Research. CRC Press. New York.
Chen, Y. C., Sheng, W. H., Wang, J. T., Chang, S. C., Lin, H. C., Tien, K. L., Hsu, L. Y., \& Tsai, K. S. (2011). Effectiveness and limitations of hand hygiene promotion on decreasing healthcare-associated infections. PLoS One, 6(11), e27163. https://doi.org/10.1371/journal.pone.0027163
Mathur, P. (2011). Hand hygiene: back to the basics of infection control. Indian J Med Res, 134(5), 611-620. https://doi.org/10.4103/0971-5916.90985
WHO. (2009). In WHO Guidelines on Hand Hygiene in Health Care: First Global Patient Safety Challenge Clean Care Is Safer Care. https://www.ncbi.nlm.nih.gov/pubmed/23805438
Yang, L., Lu, Y., Cao, J., Huang, J., \& Zhang, M. (2020). E-Tree Learning: A Novel Decentralized Model Learning Framework for Edge AI. IEEE Internet of Things Journal.
Cane, J., O'Connor, D., \& Michie, S. (2012). Validation of the theoretical domains framework for use in behaviour change and implementation research. Implementation science, 7(1), 37.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Scanner Feedback + Instructional Video | Active comparator | Behavioral: Instructional Video + Scanner FeedbackAll participants first perform a baseline handwash with fluorescent powder (no guidance). In this arm, participants view their baseline fluorescent residue results (Semmelweis Scanner™) and then watch a standard 7-step instructional video. They immediately perform a second handwash (post-training). Outcomes include change in fluorescent residue (%) and technique quality. |
| Edge AI-based AR Hand Hygiene Training | Experimental | Device: Edge AI-based AR Hand Hygiene Training SystemAll participants first perform a baseline handwash with fluorescent powder (no guidance). In this arm, participants do not view their baseline fluorescent residue. They proceed directly to AI-based AR training that provides real-time individualized feedback on the 7-step technique, then immediately perform a second handwash (post-training). Outcomes include change in fluorescent residue (%) and technique quality. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Undergraduate students enrolled in health-related disciplines (e.g., nursing, medicine, rehabilitation sciences, medical laboratory science) at participating universities
- Healthcare professionals or supporting staff working in participating hospitals
- Able to provide informed consent
- Willing to participate in both pre- and post-training assessments during the same study visit
- Aged 18 years or above
Key exclusion criteria (4 listed)
- Known allergy or skin irritation to fluorescent powder or hand hygiene products
- Current visible skin conditions (e.g., dermatitis, eczema, open wounds) on hands that may interfere with handwashing assessment
- Unable to understand or follow the training instructions
- Refusal or inability to provide written informed consent
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Instructional Video + Scanner FeedbackViewing quantified fluorescent residue from the first handwash plus a standard 7-step instructional video prior to the second handwash. | Behavioural | Scanner Feedback + Instructional Video |
| Edge AI-based AR Hand Hygiene Training SystemAn edge AI + AR system using computer vision to assess handwashing performance and deliver real-time, individualized guidance before the second handwash. | Device | Edge AI-based AR Hand Hygiene Training |
Primary outcome
Change in decontamination effectiveness (percentage of fluorescent residue on both hands)
Time frame: Immediately after intervention (within the same study visit)
The main outcome assesses the effectiveness of hand hygiene training by measuring the change in residual fluorescent powder percentage between the first (pre-training) and second (post-training) handwashing attempts. Fluorescent residue will be quantified using the Semmelweis Scanner™ to objectively evaluate handwashing effectiveness.
1 secondary outcome
Change in hand hygiene knowledge and self-reported practice scores
Time frame: Immediately after intervention (within the same study visit)
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Dec 2025.
- Background: PubMed 22530986Cane J, O'Connor D, Michie S. Validation of the theoretical domains framework for use in behaviour change and implementation research. Implement Sci. 2012 Apr 24;7:37. doi: 10.1186/1748-5908-7-37.
- Background: PubMed 22110610Chen YC, Sheng WH, Wang JT, Chang SC, Lin HC, Tien KL, Hsu LY, Tsai KS. Effectiveness and limitations of hand hygiene promotion on decreasing healthcare-associated infections. PLoS One. 2011;6(11):e27163. doi: 10.1371/journal.pone.0027163. Epub 2011 Nov 16.
- Background: PubMed 40605095Shin J, Kang EM, Lee SH, Heo M, Lee YJ, Lee SJ, Hong SJ, Kim JS, Kim BK, Ko YG, Choi D, Hong MK, Jang Y, Ahn CM. Prognostic implication of venoarterial extracorporeal membrane oxygenation in acute myocardial infarction-related cardiogenic shock. J Intensive Care. 2025 Jul 2;13(1):38. doi: 10.1186/s40560-025-00807-w.
- Background: PubMed 21146207Allegranzi B, Bagheri Nejad S, Combescure C, Graafmans W, Attar H, Donaldson L, Pittet D. Burden of endemic health-care-associated infection in developing countries: systematic review and meta-analysis. Lancet. 2011 Jan 15;377(9761):228-41. doi: 10.1016/S0140-6736(10)61458-4. Epub 2010 Dec 9.
- In WHO Guidelines on Hand Hygiene in Health Care: First Global Patient Safety Challenge Clean Care Is Safer Care.Link provided by the sponsor.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
3 sites in 2 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Instructional Video + Scanner Feedback and Edge AI-based AR Hand Hygiene Training System in people with Hand Hygiene Training and Infection Prevention and Control, run by The Hong Kong Polytechnic University at 3 sites in 2 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 12 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in Hong Kong, China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Lin Yang, Doctor (+852 2766 6398, l.yang@polyu.edu.hk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in decontamination effectiveness (percentage of fluorescent residue on both hands) (time frame: Immediately after intervention (within the same study visit)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07280026, which also lists 4 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Dec 2025.