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Published on in Vol 11 (2024)

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/57658, first published .
Evaluating the Construct Validity of the Charité Alarm Fatigue Questionnaire using Confirmatory Factor Analysis

Evaluating the Construct Validity of the Charité Alarm Fatigue Questionnaire using Confirmatory Factor Analysis

Evaluating the Construct Validity of the Charité Alarm Fatigue Questionnaire using Confirmatory Factor Analysis

Authors of this article:

Maximilian Markus Wunderlich1 Author Orcid Image ;   Henning Krampe2 Author Orcid Image ;   Kristina Fuest3 Author Orcid Image ;   Dominik Leicht4 Author Orcid Image ;   Moriz Benedikt Probst5 Author Orcid Image ;   Julian Runge6 Author Orcid Image ;   Sebastian Schmid7 Author Orcid Image ;   Claudia Spies2 Author Orcid Image ;   Björn Weiß2 Author Orcid Image ;   Felix Balzer1 Author Orcid Image ;   Akira-Sebastian Poncette1, 2 Author Orcid Image ;   Study Group1 ;   CAFQa Study Group Germany
Article Authors Cited by Tweetations Metrics

    1Institute of Medical Informatics, Charité–Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, , Charitéplatz 1, Berlin, , Germany

    2Department of Anesthesiology and Intensive Care Medicine CVK/CCM, Charité–Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, , Berlin, , Germany

    3Department of Anaesthesiology & Intensive Care Medicine, Klinikum Rechts der Isar, School of Medicine, Technical University Munich, , Munich, , Germany

    4Department for Anaesthesiology, Intensive Care Medicine and Pain Therapy, Justus Liebig University, , Giessen, , Germany

    5Department for Anaesthesiology, Intensive Care Medicine and Pain Therapy, Vivantes Klinikum im Friedrichshain, , Berlin, , Germany

    6Department for Anesthesiology, Surgical Intensive Care, Pain and Palliative Medicine, Marien Hospital Herne–Universitätsklinikum der Ruhr-Universität Bochum, , Herne, , Germany

    7Department of Anesthesiology and Intensive Care Medicine, University Hospital Ulm, Ulm University, , Ulm, , Germany

    8Aghamov Mirza, Blobner Manfred, Frey Ulrich, Heymann Christian von, Holan Jacqueline, Jungwirth Bettina, Popovic Dragutin, Sander Michael

    *these authors contributed equally

    Corresponding Author:

    Akira-Sebastian Poncette, PD, Dr med


    Background: The Charité Alarm Fatigue Questionnaire (CAFQa) is a 9-item questionnaire that aims to standardize how alarm fatigue in nurses and physicians is measured. We previously hypothesized that it has 2 correlated scales, one on the psychosomatic effects of alarm fatigue and the other on staff’s coping strategies in working with alarms.

    Objective: We aimed to validate the hypothesized structure of the CAFQa and thus underpin the instrument’s construct validity.

    Methods: We conducted 2 independent studies with nurses and physicians from intensive care units in Germany (study 1: n=265; study 2: n=1212). Responses to the questionnaire were analyzed using confirmatory factor analysis with the unweighted least-squares algorithm based on polychoric covariances. Convergent validity was assessed by participants’ estimation of their own alarm fatigue and exposure to false alarms as a percentage.

    Results: In both studies, the χ2 test reached statistical significance (study 1: χ226=44.9; P=.01; study 2: χ226=92.4; P<.001). Other fit indices suggested a good model fit (in both studies: root mean square error of approximation <0.05, standardized root mean squared residual <0.08, relative noncentrality index >0.95, Tucker-Lewis index >0.95, and comparative fit index >0.995). Participants’ mean scores correlated moderately with self-reported alarm fatigue (study 1: r=0.45; study 2: r=0.53) and weakly with self-perceived exposure to false alarms (study 1: r=0.3; study 2: r=0.33).

    Conclusions: The questionnaire measures the construct of alarm fatigue as proposed in our previous study. Researchers and clinicians can rely on the CAFQa to measure the alarm fatigue of nurses and physicians.

    Trial Registration: ClinicalTrials.gov NCT04994600; https://www.clinicaltrials.gov/study/NCT04994600

    JMIR Hum Factors 2024;11:e57658

    doi:10.2196/57658

    Keywords

    patient monitoring; intensive care unit; alarm; alarms; validity; validation; safety; intensive; care; alarm fatigue; alarm management; patient safety; ICU; alarm system; alarm system quality; medical devices; clinical alarms; questionnaire; questionnaires; warning; factor analysis 


    Background

    Alarm fatigue is a phenomenon where health care workers in intensive care units (ICUs) become desensitized to alarms of medical devices [1]. It can make ICU staff feel stressed, and it is a substantial risk to patient safety, as it can lead to alarms being missed or acknowledged with delay [2]. When implementing interventions or IT solutions [3] that try to remedy alarm fatigue, clinicians and clinical alarm researchers need a reliable way to assess whether they were successful. However, they have not yet agreed on a standardized way of measuring alarm fatigue [4,5], even though it was recognized more than 2 decades ago [6].

    Solely analyzing an ICU’s alarm log data cannot serve as a measure of staff’s alarm fatigue. While it is a valuable method for designing alarm management interventions [7], there is no clear association between the number of alarms on an ICU and staff’s subjective alarm fatigue. For example, simply focusing on the number of alarms disregards their temporal distribution (eg, it might fatigue staff more if alarms came in random bursts than if they were evenly spaced out [8]). This could be one of the reasons why in their intervention study, Sowan et al [9] did not find that staff’s alarm fatigue improved despite having managed to significantly reduce the number of alarms on their ICU.

    Therefore, we recently developed the Charité Alarm Fatigue Questionnaire (CAFQa), which is a 9-item questionnaire that measures alarm fatigue in nurses and physicians [10]. Using exploratory factor analysis, we identified 2 correlated factors: one revolving around the psychophysiological effects of alarms (eg, headaches and feelings of distraction), and one revolving around ICU staff’s alarm management strategies (eg, customization of alarm limits). We named the former the “alarm stress scale” and the latter the “alarm coping scale.” The alarm coping scale consists of items that are reversely scored. Hence, a high score on either scale is indicative of alarm fatigue.

    When developing a new questionnaire, it is essential to establish construct validity, that is, whether the questionnaire truly measures what it attempts to measure. One way to test an instrument’s construct validity is to administer it to a different sample and test whether the originally proposed factor structure reemerges using confirmatory factor analysis [11,12] (for a recent example see Canivez et al [13]).

    Aim

    We aim to validate the exploratively derived factor structure of the CAFQa and thus underpin the instrument’s construct validity.


    Ethical Considerations

    The ethical approval for this study was granted by the ethics committee of the Charité–Universitätsmedizin Berlin (EA4/218/20) and, if required, confirmed by the local ethics committee at the participating hospital. This study was conducted in compliance with the relevant guidelines and regulations. All participants voluntarily agreed to take part after being fully informed about the study. In study 1, as a reward for completing the questionnaire, we offered participants the chance to enter a draw where they could win a €50 (US $53) voucher for online shopping. Participants were asked to consent to have their data collected, analyzed, and stored anonymously.

    Participants

    In both studies, we included nurses, physicians, and nurses in training, while excluding other professions and non-ICU staff.

    Study 1

    We recruited participants from 9 ICUs of 5 large German hospitals. The questionnaire was administered on the web using REDCap (Research Electronic Data Capture; Vanderbilt University) between October 2021 and July 2022.

    Study 2

    Using a mailing list, we invited all members of the German Society of Anaesthesiology and Intensive Care Medicine [14] to fill out the web-based questionnaire (again using REDCap) between March 2023 and July 2023.

    Questionnaire

    The questionnaire used in both studies was identical and consisted of all 9 items from the CAFQa [10] and 5 general questions about the alarm situation in participants’ ICUs. These general questions were not part of the analysis for this report. All 14 items were pseudorandomly arranged and required responses on a Likert scale ranging from −2 (indicating “I do not agree at all”) to 2 (indicating “I very much agree”). Items with negative valences were reverse scored. Demographic items asked participants about their average number of workdays in an intensive care or monitoring area, their number of years and months of ICU experience, their workplace (campus and unit), and their profession. We made small adjustments to the original wording of 2 items (items 8 and 9) to improve readability: In item 8 we used “situation” instead of “urgency.” In item 9 we used the phrase “clinical pictures” instead of “clinical symptoms.”

    Statistical Analysis

    All analyses were conducted in R (version 4.2.1; R Foundation for Statistical Computing) using the following packages: Tidyverse [15], reshape2 [16], psych, semPlot [17], and lavaan [18]. For study 1, we pooled the data from the participating hospitals.

    Missing Data

    In accordance with Heymans and Eekhout [19], we used predictive mean matching via the mice package [20] to impute missing data that were assumed to be missing at random (MAR). We did not impute questionnaires that were either completely empty or terminated prematurely (presumably due to survey fatigue), as the assumption of MAR was not met in these cases. We assumed that survey fatigue occurred if a participant failed to respond to at least the final 20% of the questionnaire (ie, the last 3 or more of the 9 items of the CAFQa plus the 5 general questions). In total, 0.3% of the data were MAR.

    Testing Assumptions of Confirmatory Factor Analysis

    In both studies, the results of the Mardia test indicated that the multivariate skew did not come from a normal distribution with P<.001. Outliers were identified using Mahalanobis distances, with none being detected in study 1 and 4 being detected in study 2 (for both studies: χ29 cutoff=27.9; P<.001). Visual inspection of the data from all 4 cases revealed no unusual response patterns. Given the large sample size, we decided not to remove any outliers. The Kaiser-Meyer-Olkin statistic [21] in study 1 was 0.76, and in study 2 it was 0.8. In both studies, the Bartlett test of sphericity [22] rejected the null hypothesis that the correlation matrix was an identity matrix (study 1: χ236=438.3; P<.001; study 2: χ236=2495.4). There was no evidence of multicollinearity in either study as the determinant of both R matrices was greater than 0.00001 [23] and no correlations were greater than |0.7|. Overall, these results suggest that the data of both studies were suitable for factor analysis.

    Confirmatory Factor Analysis

    For both studies, we specified the model in line with our previous findings [10], with 2 correlated latent factors, labeled “alarm stress” and “alarm coping.” Items 1‐5 were assigned to “alarm stress.” Items 5‐9 were assigned to “alarm coping.” Since all CAFQa items are ordered categorical variables (due to being measured on a 5-point Likert scale) and because the Mardia tests indicated that the multivariate skew of both studies did not come from a normal distribution, we used the unweighted least-squares (ULS) algorithm based on polychoric covariances for estimating factor loadings [24-26]. We assessed the goodness-of-fit of the model using χ2, and the following fit indices in line with the cutoff criteria defined by Hu and Bentler [27]: root mean square error of approximation (RMSEA), relative noncentrality index (RNI), Tucker-Lewis index (TLI), standardized root mean squared residual (SRMR), and comparative fit index (CFI).

    Convergent Validity

    At the end of the questionnaire in both studies, we provided participants with a brief description of alarm fatigue and asked them to estimate their personal alarm fatigue as a percentage (0% indicating no alarm fatigue and 100% indicating extreme alarm fatigue). We also asked participants to provide their perceived rate of false alarms in their ICU as a percentage (0% indicating no false alarms, 100% indicating no true alarms). To measure convergent validity, we correlated the participants’ mean scores on the questionnaire with the self-provided alarm fatigue and false alarm rate estimations (in total and per factor).

    Internal Consistency

    As a measure of internal consistency, we report Cronbach coefficient α, the McDonald coefficient ω [28], and the mean interitem correlation for both factors.


    Participants

    Study 1

    We received 363 submissions. Among these, 23 came from participants who did not consent to have their data analyzed, 67 questionnaires were empty, and 8 showed signs of survey fatigue. Therefore, the sample size for this study was 265. The number of participants was roughly similar for each hospital (Giessen: n=43; Herne: n=50; Munich: n=64; Ulm: n=57; Vivantes: n=51). Most participants were nurses (n=150, 56.6%) and 35.8% (n=95) were physicians. A few participants (n=9, 3.4%) were supporting nurses, nurses in training, medical students, or interns, while 4.2% (n=11) did not state their profession.

    Study 2

    Of the 1564 submissions we received, 69 came from participants who refused to consent to have their data processed and 223 were empty questionnaires. We suspected survey fatigue in 60 cases. Hence, the sample size of study 2 was 1212. Contrary to study 1, more participants were physicians (n=1002, 82.7%) than nurses (n=186, 15.3%). Again, the group of supporting nurses, nurses in training, medical students, and interns was a minority (n=6, 0.5%). Among the participants, 1.5% (n=18) did not state their profession.

    Confirmatory Factor Analysis

    Descriptive statistics of both studies are presented in Table 1 for each item.

    Table 1. Descriptive statistics for each item and the pattern coefficients found in the confirmatory factor analysis of the 2-factor model in both studies. All loadings were statistically significant at P<.001.
    ItemDescriptionStudy 1Study 2
    Factor 1 (95% CI)Factor 2 (95% CI)Mean (SD)KurtosisSkewFactor 1 (95% CI)Factor 2 (95% CI)Mean (SD)KurtosisSkew
    1With too many alarms on my ward, my work performance, and motivation decrease.0.730 (0.643‐0.818)—a0.47 (1.01)–0.62–0.30.677 (0.636‐0.717)—0.51 (1.08)–0.63–0.37
    2Too many alarms trigger physical symptoms for me, e.g., nervousness, headaches, and sleep disturbances.0.706 (0.612‐0.800)—0.23 (1.26)–1.13–0.160.694 (0.653‐0.735)—0.22 (1.20)–1.00–0.14
    3Alarms reduce my concentration and attention.0.725 (0.635‐0.814)—0.43 (1.07)–0.91–0.210.813 (0.779‐0.846)—0.63 (1.03)–0.59–0.39
    4My or neighboring patients’ alarms or crisis alarms frequently interrupt my workflow.0.432 (0.318‐0.547)—0.87 (0.83)–0.41–0.390.519 (0.469‐0.570)—0.70 (0.87)–0.28–0.37
    5There are situations when alarms confuse me.0.488 (0.384‐0.593)—0.08 (1.09)–0.73–0.090.634 (0.592‐0.676)—0.19 (1.07)–0.85–0.04
    6In my ward, procedural instruction on how to deal with alarms is regularly updated and shared with all staff.b—0.434 (0.270‐0.598)0.77 (1.24)–0.68–0.7—0.449 (0.375‐0.5231.10 (1.02)0.44–1.06
    7Responsible personnel respond quickly and appropriately to alarms.b—0.587 (0.424‐0.750)-0.32 (0.82)–0.12–0.12—0.639 (0.567‐0.711–0.39 (0.90)–0.050.19
    8The acoustic and visual monitor alarms used on my ward floor and in my nurses’ station allow me to assign the patient, the device, and the situation clearly.b—0.349 (0.182‐0.517)-0.46 (1.06)–0.520.36—0.428 (0.359‐0.498–0.36 (1.15)–0.660.32
    9Alarm limits are regularly adjusted based on patients’ clinical pictures (e.g., blood pressure limits for conditions after bypass surgery).b—0.581 (0.428‐0.734)-0.38 (0.93)–0.240.26—0.575 (0.508‐0.641–0.35 (0.94)–0.120.40

    aNot applicable.

    bItem with a negative valence that is reversely scored.

    Study 1

    While the χ2 test was significant at α=.05 with χ226=44.9 (P=.01), indicating that the model did not fit the data, all fit indices suggested a good model fit: RMSEA=0.03, SRMR=0.052, RNI=0.989, TLI=0.985, and CFI=0.989. All items loaded onto their hypothesized factors as expected, with factor loadings that were statistically significant at P<.001, ranging from 0.35 to 0.73. The factors were moderately correlated at 0.4 (95% CI 0.21‐0.59; P<.001).

    Study 2

    As in study 1, the χ2 test was significant (χ226=92.4; P<.001), indicating that the model did not fit the data, while the fit indices showed a good model fit: RMSEA=0.046, SRMR=0.041, RNI=0.982, TLI=0.975, and CFI=0.982. Again, all items loaded onto their hypothesized factors as expected, with factor loadings that were statistically significant at P<.001, ranging from 0.43 to 0.81. The factors were moderately correlated at 0.44 (95% CI 0.36‐0.51; P<.001) (Figure 1).

    ‎
    Figure 1. Diagram of the final model from each study. Factors are shown in circles (factor 1: alarm stress; factor 2: alarm coping), and items 1‐9 in squares. In both studies, the variance of the factors was constrained to 1. The arrows connecting the factors with the items are the factor loadings and arrows pointing toward the items show the residuals. The arrows between the factors show their correlation.

    Convergent Validity

    In study 1, the participants’ mean scores on the questionnaire correlated moderately with self-reported alarm fatigue (r242=0.45, 95% CI 0.34-0.54; P<.001) and weakly with the perceived percentage of false alarms (r247=0.3, 95% CI 0.18 to –0.41; P<.001). Similar patterns were observed in study 2 (Table 2 provides full details).

    Table 2. Correlation coefficients, P values, and CIs used to investigate the convergent validity in each study.
    Study and correlation measurer (df; 95% CI)P value
    Study 1
    MS-SRAFab0.45 (242; 0.34‐0.54)<.001
    F1S-SRAFc0.42 (242; 0.31‐0.52)<.001
    F2S-SRAFd0.29 (242; 0.17‐0.4)<.001
    MS-PPFAe0.30 (247; 0.18‐0.41)<.001
    F1S-PPFA0.20 (247; 0.08‐0.32).002
    F2S-PPFA0.29 (247; 0.17‐0.4)<.001
    Study 2
    MS-SRAF0.53 (1180; 0.49‐0.57)<.001
    F1S-SRAF0.49 (1180; 0.45‐0.53)<.001
    F2S-SRAF0.34 (1180; 0.29‐0.39)<.001
    MS-PPFA0.33 (1182; 0.28‐0.38)<.001
    F1S-PPFA0.26 (1182; 0.21‐0.32)<.001
    F2S-PPFA0.28 (1182; 0.23‐0.33)<.001

    aMS: mean score on the questionnaire.

    bSRAF: self-reported alarm fatigue.

    cF1S: scores on factor 1.

    dF2S: scores on factor 2.

    ePPFA: perceived percentage of false alarms.

    Internal Consistency

    In study 1, the Cronbach α of factor 1 was 0.72, and it was 0.49 for factor 2. Cronbach α across factors was 0.67. The mean interitem correlation on factor 1 was 0.38, and it was 0.23 on factor 2. The McDonald coefficient ω for factor 1 was 0.77, and for factor 2 it was 0.55. The overall coefficient ω for the assessment was 0.8.

    Results were similar in study 2: the Cronbach α was 0.77 for factor 1 and 0.55 for factor 2. Cronbach α across factors was 0.72. The mean interitem correlation was 0.44 on factor 1 and 0.27 on factor 2. The McDonald coefficient ω was 0.8 for factor 1 and 0.59 for factor 2. The overall coefficient ω for the assessment was 0.85.


    We aimed to underpin the construct validity of the CAFQa by submitting the exploratively derived factor structure from our previous study to confirmatory factor analysis in 2 independent studies. While the χ2 test rejected the model in both studies, all fit indices indicated a good model fit. The factor loadings ranged from 0.35 to 0.73 in study 1 and from 0.43 to 0.81 in study 2; all were statistically significant. Overall, these results support the hypothesized factor structure. The questionnaire seems to measure the construct of alarm fatigue as proposed in our previous work [10].

    The χ2 test is known to be sensitive to large sample sizes [29], which might explain its statistical significance. We did not modify the model because all fit indices indicated a good fit and because model modifications, no matter how small or plausible, can make a model less generalizable.

    In both studies, the first factor, that is, the alarm stress scale, and the overall questionnaire were internally consistent. However, the second factor, that is, the alarm coping scale, seems to have issues with its internal consistency. Here, Cronbach α and McDonald ω were 0.49 and 0.55 in study 1, respectively, and 0.55 and 0.59 in study 2, respectively. A similar pattern can be found in our previous study, where the Cronbach α of factor 2 was 0.57 [10]. An internally consistent questionnaire is desirable. However, it can also mean that items are very similar. It was our ambition to create a questionnaire that is brief while measuring the many facets of alarm fatigue. Future studies using the CAFQa should routinely assess the internal consistency of both factors. If the second factor continues to show medium internal consistency, research should be done on how it can be improved (eg, by adding additional items, which would come at the cost of a longer questionnaire).

    Because no other measures of alarm fatigue exist that would allow us to estimate the CAFQa’s convergent validity, we asked participants to rate their own alarm fatigue as well as the rate of false alarms they perceived in their daily work. Participants who had a high mean score on the questionnaire also rated themselves as more alarm fatigued (r=0.45 in study 1 and r=53 in study 2). This positive correlation indicates the convergent validity of the questionnaire. Similarly, both studies demonstrated that participants with a high mean score on the questionnaire perceived more alarms to be false in their ICU. In study 1 this association was stronger for factor 2 than for factor 1. This makes sense since a high score on factor 2 (ie, the alarm coping scale) indicates that alarms are not properly managed (eg, by means of patient-specific threshold customizations), which typically leads to more false alarms [30]. However, study 2 could not replicate this pattern. Future research should find an answer to this question: Do ICU staff with a high perceived percentage of false alarms tend to develop stronger alarm fatigue, or do staff that are more alarm fatigued tend to perceive more alarms as being false?

    Limitations

    The fit indices RMSEA, CFI, and TLI have been shown to overestimate model fit when using the ULS estimator [31,32], potentially leading researchers to accept a bad-fitting model. Yet, in our case, other fit indices indicated a good model fit. As in our previous work [10], the assumption that participants can accurately reflect and express their own alarm fatigue as a percentage is likely flawed (otherwise, it would not be necessary to develop a questionnaire in the first place). However, most ICU nurses and physicians have heard of alarm fatigue, and we provided them with a brief recapitulation on the concept before having them answer the self-report item in each study. Likewise, it is also probably a flawed assumption that participants can accurately report the rate of false alarms, though Bliss et al [33] showed that participants were able to adapt their response frequencies to alarms based on to the perceived probability that an alarm was not false, thus suggesting that people might have an intuitive grasp of the rate of false alarms in their unit. All in all, we believe that asking these self-rating questions is a valuable method for assessing convergent validity when no other instrument is available.

    Conclusion

    Our results from 2 independent studies underpin the construct validity of the CAFQa. All items consistently loaded onto the factors, as we proposed in a previous publication [10]. When conducting research or quality improvement projects in ICUs, clinical alarm researchers and clinicians can rely on this instrument to measure, compare, and benchmark the alarm fatigue of nurses and physicians.

    Acknowledgments

    ASP is a participant in the Charité Digital Clinician Scientist Program funded by the Charité–Universitätsmedizin Berlin and the Berlin Institute of Health. We are grateful to Nicolas Frey for supervising the logistical aspects of the survey distribution, to Sandro Amende-Wolf for his valuable clinical insights, and to Daniel Schulze for his critical examination of our statistical analysis. We are grateful to the German Society of Anaesthesiology and Intensive Care Medicine for the distribution of the questionnaire to its members. This article was extracted from the doctoral thesis of MMW.

    Data Availability

    The data sets generated and analyzed during the current study are available in the Zenodo repository [34].

    Authors' Contributions

    MMW, CS, FB, and ASP conceptualized the study. MMW, KF, DL, MBP, JR, and SS conducted the investigation. MMW and HK developed the study design and ensured methodological rigor. MMW, BW, and ASP contributed to the formal data analysis. MMW and ASP drafted the initial manuscript and contributed to its revision. MMW created all figures and tables and managed the project together with ASP. HK, KF, DL, MBP, JR, SS, CS, BW, FB, and ASP reviewed the manuscript. FB and ASP provided oversight and leadership throughout the study.

    Ulrich Frey (Department for Anesthesiology, Surgical Intensive Care, Pain and Palliative Medicine, Marien Hospital Herne–Universitätsklinikum der Ruhr-Universität Bochum, Herne, Germany), Christian von Heymann (Department for Anaesthesiology, Intensive Care Medicine and Pain Therapy, Vivantes Klinikum im Friedrichshain, Berlin, Germany), Jacqueline Holan (Department for Anaesthesiology, Intensive Care Medicine and Pain Therapy, Vivantes Klinikum im Friedrichshain, Berlin, Germany), Bettina Jungwirth (Department of Anesthesiology and Intensive Care Medicine, University Hospital Ulm, Ulm University, Ulm, Germany), Dragutin Popovic (Department for Anaesthesiology, Intensive Care Medicine and Pain Therapy, Vivantes Klinikum im Friedrichshain, Berlin, Germany ), and Michael Sander (Department for Anaesthesiology, Intensive Care Medicine and Pain Therapy, Justus Liebig University, Giessen, Germany).

    Conflicts of Interest

    None declared.

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    ‎
    CAFQa: Charité Alarm Fatigue Questionnaire
    CFA: confirmatory factor analysis
    CFI: comparative fit index
    EFA: exploratory factor analysis
    ICU: intensive care unit
    MAR: missing at random
    REDCap: Research Electronic Data Capture
    RMSEA: root mean square error of approximation
    RNI: relative noncentrality index
    SRAF: self-reported alarm fatigue
    SRMR: standardized root mean squared residual
    TLI: Tucker-Lewis index
    ULS: unweighted least-squares

    Edited by Daniel Gooch; submitted 28.02.24; peer-reviewed by Joseph Schlesinger, Kaio Bin, Keisuke Takano; final revised version received 02.05.24; accepted 02.05.24; published 08.08.24.

    Copyright

    © Maximilian Markus Wunderlich, Henning Krampe, Kristina Fuest, Dominik Leicht, Moriz Benedikt Probst, Julian Runge, Sebastian Schmid, Claudia Spies, Björn Weiß, Felix Balzer, Akira-Sebastian Poncette, CAFQa Study Group Germany. Originally published in JMIR Human Factors (https://humanfactors.jmir.org), 8.8.2024.

    This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR Human Factors, is properly cited. The complete bibliographic information, a link to the original publication on https://humanfactors.jmir.org, as well as this copyright and license information must be included.