The study protocol was reviewed and approved by the Ethics Committee of Guangzhou Panyu Shiqiao Hospital (Approval Number: ASJIO729). Because the study strictly used routinely collected, de-identified ward-level quality-improvement and infection-control indicators, the ethics committee explicitly waived the requirement for individual informed consent. No patient names, staff names, medical record numbers, or other directly identifiable information were included in the analytical dataset, and data access was restricted to authorized members of the study team.
Study design
This controlled before-and-after study evaluated the effect of a PDCA-based hand hygiene governance bundle on hand hygiene compliance, hospital-acquired infection rates, and nursing management quality in inpatient wards. The study used the ward-month as the main analytical unit and compared changes between intervention wards and control wards across a pre-intervention and post-intervention period. The methodological structure followed quality improvement reporting principles described in SQUIRE 2.013.
The study workflow is shown in Figure 1, including ward selection, group allocation, baseline observation, intervention implementation, monthly outcome assessment, and repeated PDCA cycles. Baseline ward-level characteristics during the pre-intervention period are summarized in Table 1.
Setting and study period
The study was conducted in 16 inpatient wards of a general hospital, which comprises a total of 32 inpatient wards. Eight wards were assigned to the intervention group, and eight to the control group. Ward allocation was based on the hospital's administrative and infection-control implementation planning rather than individual randomization. Strict randomization was not practically feasible for two primary reasons. First, the PDCA governance bundle required intensive logistical coordination, including specialized observer training and targeted management feedback, which necessitated a guided, phased rollout rather than random assignment. Second, purposeful non-random allocation allowed hospital administrators to group wards in a manner that minimized the risk of structural and administrative cross-contamination between the intervention and control units. To reduce selection bias, intervention and control wards were selected to achieve approximate balance in ward type, baseline patient-days, baseline hand hygiene compliance, baseline hospital-acquired infection rate, and baseline nursing management quality.
The observation period covered 12 consecutive months. The first 6 months were defined as the pre-intervention period, during which both groups received routine hand hygiene management. The following 6 months were defined as the post-intervention period. During the post-intervention period, the intervention wards received the PDCA-based hand hygiene governance bundle, while the control wards continued routine infection-control management. The ward selection, exposure definition, outcome specification, and group comparison structure were organized according to observational study reporting principles14.
The ward-month was selected as the analytical unit because hand hygiene compliance, hospital-acquired infection counts, patient-days, nursing management quality scores, and process indicators were collected and summarized monthly at the ward level. Each of the 16 wards contributed 12 monthly records, resulting in 192 ward-month observations.
Study units and eligibility criteria
A ward-month record was eligible for analysis if the ward remained open for the full calendar month, admitted inpatients during that month, had complete patient-day records, had available hand hygiene observation data, and had a completed nursing management quality assessment for the same month.
Ward-month records were excluded if the ward was temporarily closed, merged with another ward, converted to another clinical function, or experienced a major service disruption that made monthly infection surveillance incomplete. Records were also excluded if any core outcome variable was missing, including hand hygiene opportunities, hand hygiene actions, patient-days, hospital-acquired infection counts, or nursing management quality scores.
Healthcare workers included in hand hygiene observation were nurses, physicians, and care assistants who provided direct patient care in the participating wards. Observations involving administrative personnel, visitors, students without independent clinical duties, temporary visitors, or staff not involved in direct patient care were not included.
Intervention: PDCA-based hand hygiene governance bundle
The intervention was a structured hand hygiene governance bundle implemented through repeated Plan–Do–Check–Act cycles. The bundle combined baseline gap analysis, staff training, workflow reminders, supply monitoring, direct observation of hand hygiene, audit feedback, ward-level accountability, and targeted corrective actions. The intervention structure followed the core components of multimodal hand hygiene improvement, including system change, education, evaluation and feedback, reminders, and safety climate reinforcement6.
During the Plan phase, the infection-control team reviewed baseline hand hygiene compliance, hand hygiene opportunities, hospital-acquired infection rates, alcohol-based hand rub consumption, and nursing management quality scores in each intervention ward. The team identified ward-specific problems, including low compliance before patient contact, missed hand hygiene before aseptic procedures, inconsistent use of alcohol-based hand rub, delayed feedback after audit, and incomplete linkage between hand hygiene performance and nursing management review. Each intervention ward developed a monthly improvement plan specifying the target problem, the person responsible, the expected completion time, the follow-up method, and the measurable target.
During the Do phase, the planned improvement measures were implemented. Each intervention ward received one structured training session at the beginning of the intervention period and one brief refresher session each month. Each session lasted approximately 20–30 min and was delivered by infection-control nurses. Training covered hand hygiene indications, correct use of alcohol-based hand rub, handwashing technique, glove use, and infection-control risk points. Visual reminders were placed near patient bedsides, treatment rooms, medication preparation areas, nursing stations, and ward entrances. The accessibility of alcohol-based hand rub was checked weekly. Empty, misplaced, or poorly accessible dispensers were corrected within 24 h by the ward nursing team. Head nurses organized short ward-level briefings to reinforce hand hygiene requirements during routine nursing management.
During the Check phase, trained observers conducted monthly hand hygiene observations. Observers recorded approximately 180–260 hand hygiene opportunities per ward per month, depending on ward workload and patient care activities. To systematically mitigate the Hawthorne effect, these observations were not conducted in single, prolonged blocks. Instead, they were divided into unannounced, short-duration sessions (typically 15–20 min) that were randomly distributed across various days of the week, including weekends, and across multiple working shifts. A ward-month was considered observation-complete when at least 150 valid hand hygiene opportunities were recorded. If fewer than 150 valid opportunities were recorded because of low activity or incomplete observation coverage, an additional observation session was arranged within the same month. Each observation recorded the professional role of the healthcare worker, the hand hygiene moment, the number of opportunities, and whether the required hand hygiene action was performed. Hand hygiene opportunities were classified according to the five indications of hand hygiene: before touching a patient, before clean or aseptic procedures, after body fluid exposure risk, after touching a patient, and after touching patient surroundings1.
During the Act phase, the intervention team used monthly findings to revise the next improvement cycle. Each intervention ward received a monthly feedback report that included overall hand hygiene compliance, compliance by professional role, compliance by hand hygiene moment, alcohol-based hand rub consumption, hospital-acquired infection rate, and nursing management quality score. Corrective action was triggered when any of the following criteria were met: monthly hand hygiene compliance below 80%, compliance for any professional group below 75%, compliance for any hand hygiene moment below 70%, hospital-acquired infection rate increasing by at least 20% compared with the ward’s pre-intervention mean, or repeated documentation problems in nursing management quality assessment. Wards meeting any trigger criterion completed a corrective action form within 7 days and received focused supervision in the following month. If a specific hand hygiene moment or professional group showed lower compliance, corrective actions were directed to that problem rather than repeated as general education. The next PDCA cycle then began with an updated problem list and revised ward-level improvement target.
Control condition and contamination control
Control wards continued routine hand hygiene management during the same study period. Routine management included standard infection-control policies, availability of alcohol-based hand rub, routine hand hygiene reminders, and regular infection-control supervision. Control wards did not receive the structured monthly PDCA cycle, ward-specific feedback reports, corrective action forms, intensified observation feedback, or targeted governance meetings used in the intervention wards.
To reduce contamination between groups, intervention-specific feedback reports, corrective action forms, ward-level PDCA records, and monthly improvement meetings were not circulated to control wards during the study period. Hospital-wide infection-control policies that applied to all wards were maintained consistently in both groups.
Outcome measures
The primary outcome was monthly hand hygiene compliance, assessed via direct human observation. Compliance was calculated at the individual ward-month level as the total number of observed hand hygiene actions within a specific ward during a given month divided by the corresponding total number of observed hand hygiene opportunities, multiplied by 100%. A hand hygiene action was counted as valid when the healthcare worker performed hand hygiene using alcohol-based hand rub or soap-and-water handwashing immediately after a defined opportunity occurred and before moving to the next care activity. Actions performed too early, too late, or unrelated to the observed opportunity were not counted as compliant actions.
The main secondary outcome was the hospital-acquired infection rate. Hospital-acquired infections were identified through the hospital infection-control surveillance system according to institutional surveillance criteria aligned with healthcare-associated infection monitoring practice. To ensure clarity and international comparability, the composite HAI rate in this study specifically included central line-associated bloodstream infections (CLABSI), catheter-associated urinary tract infections (CAUTI), surgical site infections (SSI), hospital-acquired/ventilator-associated pneumonia (HAP/VAP), and infections caused by targeted multidrug-resistant organisms (e.g., methicillin-resistant Staphylococcus aureus and Clostridioides difficile). Suspected cases were reviewed by infection-control practitioners, and monthly ward-level counts were finalized after verification with clinical records, microbiology reports, antimicrobial use records, temperature charts, imaging reports where applicable, and ward infection-control logs. The monthly hospital-acquired infection rate was calculated as the number of hospital-acquired infection cases divided by total patient-days and multiplied by 1,000. Patient-days were used as the denominator because they represent cumulative inpatient exposure time and are commonly used in healthcare-associated infection surveillance15.
Another secondary outcome was nursing management quality. Nursing management quality was assessed monthly using a structured ward-level assessment form. The assessment covered hand hygiene governance, infection-control documentation, availability of supplies, staff training completion, audit feedback, environmental management, and corrective action implementation. Scores ranged from 0 to 100, with higher scores indicating better nursing management quality. A monthly score below 80 was treated as a management-warning value and required review by the head nurse. A score below 75 triggered a written corrective action plan.
Additional process indicators included hand hygiene knowledge score and alcohol-based hand rub consumption. Hand hygiene knowledge was assessed using a structured knowledge test, with scores ranging from 0 to 100. A score of 80 or above was considered satisfactory. Staff with scores below 80 received additional brief training before the next monthly assessment. Alcohol-based hand rub consumption was calculated as milliliters per patient-day and was evaluated as a supporting process measure to objectively corroborate the direct observation findings of hand hygiene compliance. Detailed operational definitions, thresholds, and calculation formulas are provided in Supplementary Table 1.
Data collection procedures
Data were collected monthly from each participating ward. Hand hygiene observation data were collected by trained infection-control observers using a standardized observation form. Observers recorded the ward code, month, professional role, hand hygiene moment, number of opportunities, and number of performed actions. The same observation rules were applied to intervention and control wards.
Prior to formal data collection, all observers completed standardized calibration training and achieved ≥90% inter-rater agreement using standardized clinical scenarios. Detailed protocols regarding observer training, the five indications classification, and validation criteria are provided in Supplementary File 1.
Hospital-acquired infection cases and patient-day counts were obtained from routine infection-control surveillance records. Monthly admission counts and patient-days were checked against ward administrative records before analysis. Nursing management quality scores were obtained from monthly nursing quality assessments. Alcohol-based hand rub consumption was obtained from ward supply records and standardized by patient-days.
For each ward-month, the final analytical dataset included ward code, group assignment, month, study period, PDCA stage, admissions, patient-days, hand hygiene opportunities, hand hygiene actions, hand hygiene compliance, hospital-acquired infection cases, hospital-acquired infection rate per 1,000 patient-days, nursing management quality score, hand hygiene knowledge score, and alcohol-based hand rub consumption.
Data quality control and missing data handling
Rigorous data quality control procedures were implemented to minimize measurement bias and ensure data integrity. These included concurrent temporal observations for both groups, monthly data aggregation to reduce daily fluctuation noise, and strict predefined screening for logical inconsistencies or out-of-range values. A comprehensive description of the specific data-checking algorithms, flagging thresholds, and missing data handling procedures is detailed in Supplementary File 1.
Because direct observation of hand hygiene inherently risks altering staff behavior (the Hawthorne effect), the data collection protocol mandated strictly unpredictable observation schedules. By utilizing unobtrusive, brief monitoring windows randomly dispersed across different weekdays, weekends, varied shifts (morning, afternoon, and night), professional roles, and hand hygiene moments, the study sought to capture routine clinical practice rather than conditioned compliance. The identical observation protocol was applied equally to both groups to prevent differential measurement bias (i.e., ensuring observers did not apply differing levels of scrutiny between the intervention and control wards), whereas the aforementioned randomized scheduling was explicitly implemented to minimize sampling bias.
All included ward-month records contained complete core outcome variables. Therefore, no imputation was performed. Although predefined exclusion criteria were established a priori to handle potential ward closures or missing variables, no ward-month records actually met these criteria during the study. Consequently, zero records were excluded, and all 192 planned ward-month observations were completely retained, thereby ensuring that both intervention and control groups were continuously evaluated across the exact same 12-month calendar period.
Statistical analysis
Statistical analysis was performed using SPSS and R16. Descriptive tables were generated accordingly. Specific modeling approaches were tailored to the distribution of each outcome: logistic regression for hand hygiene compliance, Poisson or negative binomial regression for hospital-acquired infection rates, and linear regression for continuous nursing management quality and knowledge scores. All statistical estimations, incorporating the difference-in-differences framework and clustered standard error computations, were executed in R utilizing the stats, MASS, sandwich, and lmtest packages. Figures were prepared using GraphPad Prism and checked against the final statistical output.
Continuous variables were summarized as mean and standard deviation when approximately normally distributed, and as median and interquartile range when the distribution was skewed. The normality of continuous variables for descriptive summaries, as well as the normality of model residuals for linear regression analyses, was assessed using histograms, Q–Q plots, and the Shapiro–Wilk test. Categorical variables were summarized as counts and percentages. Baseline comparability between intervention and control wards was assessed using pre-intervention ward-level indicators, including admissions, patient-days, hand hygiene opportunities, hand hygiene compliance, hospital-acquired infection rate, nursing management quality score, hand hygiene knowledge score, and alcohol-based hand rub consumption.
The main analysis compared pre-intervention to post-intervention changes between intervention and control wards. For hand hygiene compliance, the model incorporated the number of hand hygiene actions as the outcome of interest, while explicitly specifying the varying number of observed hand hygiene opportunities per ward-month as the binomial denominator. This specification functionally accounts for the differential observation volumes across units in a manner analogous to an offset. The intervention effect was estimated using a logistic regression model within a difference-in-differences framework, incorporating group, period, and group-by-period interaction terms. Throughout the manuscript, the term 'adjusted' applied to effect estimates (e.g., adjusted odds ratios or incidence rate ratios) explicitly denotes that these parameters were derived from these fully specified multivariable models—mathematically adjusting for the study group main effect, period main effect, variable exposure volumes, and ward-level clustering—rather than implying the inclusion of additional clinical covariates. To prevent over-parameterization, the specific calendar month was not included as a continuous or categorical covariate in these primary models, as the binary 'period' variable sufficiently captured the overarching temporal shift. However, to ensure our findings were not confounded by seasonal fluctuations, calendar month was explicitly incorporated as an additional covariate within our predefined sensitivity analyses.
To formally validate the parallel trends assumption inherent to difference-in-differences modeling, pre-intervention monthly outcomes were visually inspected to confirm that the temporal slopes for the intervention and control wards were parallel prior to implementation. Statistically, this assumption was evaluated by introducing a group-by-month interaction term into the specific regression models tailored to each respective outcome (i.e., logistic, count, and linear models) restricted solely to the pre-intervention period; a non-significant interaction (P ≥ 0.05) confirmed that the pre-intervention trends (slopes) between the two groups did not significantly diverge, irrespective of any constant absolute differences in their baseline levels. The primary models reported effect estimates with 95% confidence intervals rather than relying only on P values.
For hospital-acquired infection rates, monthly infection counts were analyzed using a count model. Specifically, these models incorporated the study group, period, and the group-by-period interaction as fixed effects. To rigorously adjust for varying baseline exposure volumes across units, the natural logarithm of monthly patient-days was defined and entered as the offset term. In alignment with our overarching analysis strategy, ward-level clustering was accounted for using cluster-robust standard errors, and thus explicit random-effects parameters were not included in the model. The final choice between the Poisson and negative binomial specifications was explicitly determined by evaluating the dispersion parameter (θ) estimated from the initial negative binomial model. The simpler Poisson model was deemed appropriate when this parameter indicated no substantial overdispersion; otherwise, the negative binomial specification was retained to account for the excess variance. The effect estimate was reported as an incidence rate ratio with 95% confidence interval. Hospital-acquired infection rates were also described as cases per 1,000 patient-days.
For nursing management quality scores and hand hygiene knowledge scores, linear regression models were used with group, period, and group-by-period interaction terms; the resulting interaction coefficient (β) represents the adjusted mean difference in score improvements between the two groups. To rigorously account for ward-to-ward variability and the non-independence of monthly data, observations were strictly not treated as independent. Across all models—including those for hand hygiene compliance, hospital-acquired infections, nursing management quality, alcohol-based hand rub consumption, and all subgroup analyses—the fixed effects consistently comprised the study group, the intervention period, and their interaction. Rather than fitting generalized linear mixed models (GLMMs) with random effects, clustering was explicitly addressed by computing cluster-robust standard errors at the ward level for every model. This approach appropriately adjusts all P values and widens the confidence intervals to correct for intra-class correlation, directly ensuring that the inferential statistics are robust and not optimistically narrow. Alcohol-based hand rub consumption was analyzed quantitatively to serve as an objective proxy measure, triangulating the behavioral changes observed in hand hygiene compliance.
Subgroup analyses were conducted by professional role and hand hygiene moment. The professional role was categorized as nurse, physician, or care assistant. Hand hygiene moment was categorized as before touching a patient, before clean or aseptic procedures, after body fluid exposure risk, after touching a patient, and after touching patient surroundings. These analyses were considered supportive because the study was primarily designed to evaluate ward-level changes rather than individual-level staff effects.
Extensive sensitivity analyses were conducted to confirm the robustness of our primary models. These included excluding the initial implementation transition month to account for phase-in effects and explicitly incorporating the calendar month as an additional covariate to adjust for potential seasonal variations. To streamline the main text, the detailed methodologies and complete results for these sensitivity analyses are provided exclusively in Supplementary File 2.
Although the intervention was hypothesized to yield beneficial outcomes, all statistical tests remained two-sided to conservatively allow for the detection of any unintended negative effects (e.g., paradoxical decreases in compliance or increases in infection rates), aligning with standard epidemiological reporting practices. A P value below 0.05 was considered statistically significant. No adjustment for multiple comparisons was applied across the primary and secondary outcomes, as these endpoints represented distinct, pre-specified domains of the intervention's impact (i.e., behavioral, clinical, and administrative dimensions) rather than multiple tests of a single hypothesis. Similarly, no adjustment was applied to the supportive subgroup analyses, which were strictly interpreted as exploration. The analysis file included data import, variable checking, descriptive summaries, baseline comparison, difference-in-differences models, count models for hospital-acquired infection rates, sensitivity analyses, subgroup analyses, and figure-ready output tables.