SMART-Pred (Shiny Multi-Algorithm R Tool for Predictive Modeling) is an innovative AI-based R Shiny application developed to address the increasing demand for accessible data science tools and to simplify the complexity of ML workflows [67,71,72]. This user-friendly platform automates essential steps, such as data preprocessing, model training, hyperparameter tuning, model validation, and performance evaluation. It features a web interface that allows users to upload and preview datasets, configure variables, and compute descriptive statistics. SMART-Pred incorporates 10 classic ML algorithms, including logistic regression, random forest, adaptive boosting (AdaBoost), support vector machine (SVM), and neural network, for robust classification tasks. The tool also offers interactive data frames for comparing model evaluation metrics, alongside visualization capabilities like multimodel receiver operating characteristic (ROC) curve comparisons, feature importance ranking (by each selected algorithm saved as a CSV file in the same working directory in addition to the graphical display), and the Shapley Additive Explanations (SHAP) framework, which can provide the direction of influence of each feature. With one-click server deployment, SMART-Pred ensures accessibility anytime and anywhere, creating a convenient and intuitive environment for ML modeling that bridges the gap between complex AI algorithms and practical applications, potentially accelerating research and innovation across data-driven fields.

The DARWIN (Diagnosis Alzheimer With Handwriting) dataset [73] was used to validate SMART-Pred’s classification capabilities and benchmark its performance against prior studies. Specifically curated for early AD detection, the DARWIN dataset comprises handwriting data from 174 participants (89 patients with AD and 85 healthy controls) across 452 columns, including unique identifiers, classification labels (“P” for patient and “H” for healthy), and 451 features extracted from 25 structured tasks (graphic, copy, memory, and dictation exercises) with 18 features per task. Collected using standardized protocols (eg, Wacom tablets at 200 Hz), this dataset captures fine motor and cognitive variations linked to neurodegeneration, offering a balanced sample to minimize algorithmic bias and richer multidimensional data compared to single-task datasets. Unlike neuroimaging-focused alternatives like Alzheimer’s Disease Neuroimaging Initiative (ADNI), the DARWIN dataset supports noninvasive, cost-effective, and immediately deployable screening in clinical settings, aligning with SMART-Pred’s goal of accessible early AD detection [73,74]. Its feature richness and task diversity mitigate overfitting risks and provide direct insights into cognitive-motor integration, a hallmark of AD progression, while prioritizing actionable, low-resource biomarkers over complex biological data, thus enabling it to offer pragmatic solutions for early diagnosis in diverse health care environments. The SMART-Pred application and data are provided in Multimedia Appendix 1.

The ultimate objective of this study is to leverage handwriting characteristics from the DARWIN dataset to distinguish between patients with AD and healthy individuals, contributing to earlier, more accessible diagnostic methods that can inform tailored interventions. We hypothesized that the integration of user-configurable and automated ML methods within the SMART-Pred workflow will enable the reliable classification of patients with AD versus healthy individuals based on handwriting features from the DARWIN dataset, demonstrating the potential of handwriting-based digital biomarkers for early, scalable AD detection. SMART-Pred’s end-to-end ML workflow for classification tasks is structured across 4 core components: data input and preview, data preprocessing, model training and validation, and model evaluation. This framework integrates user-configurable options with automated processing to ensure flexibility and methodological rigor. The process starts with data upload and preprocessing, advances through model training with multiple algorithmic choices, and culminates in comprehensive performance evaluation and visualization, as detailed in the flowchart presented in Figure 1. By democratizing access to advanced ML techniques through an intuitive interface, SMART-Pred aims to enhance research capabilities and clinical applicability in AD detection and beyond.

SHAP is a model-agnostic interpretability technique grounded in cooperative game theory, which quantifies how much each feature contributes to a model’s prediction by computing Shapley values, ensuring consistent and locally accurate explanations for individual outcomes. In its general, model-agnostic form, SHAP approximates these values using a weighted linear regression approach (Kernel SHAP), though specialized algorithms exist for specific model types. SHAP is applied to interpret predictions from all 10 ML classifiers trained on AD data, revealing the relative impact of each input feature on classification outcomes [75,76]. The explanation model g approximates the original complex model f by representing the prediction as a linear combination of feature coalitions given by:

where z` denotes a binary vector indicating the presence or absence of features in the coalition, N is the total number of AD features, and ϕi corresponds to the Shapley value, reflecting the individual feature’s contribution [77].

Through optimization, the Shapley value ϕi provides a theoretically grounded and consistent measure of feature importance, enhancing the interpretability of the ML classifier’s predictions.

SMART-Pred allows users to upload local data files through a web interface. Upon uploading, users can preview the dataset in an interactive table format (Figure 2) and access basic descriptive statistics (Figure 3). For descriptive statistics, the interface provides options for variable and measure configuration, where users can choose specific statistical measures: mean, SD, minimum, median, and maximum for numerical variables, and mode and unique count for character variables. After data upload, users proceed to configure the analysis parameters through a structured variable selection process (Figure 4). First, users specify the analysis type by selecting either “Classification” or “Regression” from the task type dropdown menu. For the target variable selection, users choose the dependent variable that represents the outcome to be predicted. The interface then presents a comprehensive list of available independent variables in a scrollable selection box, including various measurement features and other kinematic parameters. Users can either select individual variables or use the “Select all independent variables” checkbox for comprehensive analysis. This structured approach ensures proper specification of the prediction task and relevant features for subsequent analysis. The interface also provides checkboxes for selecting from 10 ML models (Figure 5).

The preprocessing pipeline (Figure 1) implements a systematic approach to data preparation. The preprocessing pipeline in SMART-Pred begins with a stratified 70‐30 split to preserve class balance between patients with AD and controls, ensuring representative distributions in the training (70%) and test (30%) sets. For missing values, mean/mode imputation is systematically applied: numerical features use subgroup-specific means (eg, imputing based on AD stage or age cohort) to retain biological context, while categorical variables use mode replacement or an “Unknown” category to avoid information loss. This approach balances simplicity with clinical relevance, as arbitrary deletion would disproportionately affect smaller AD subgroups.

Principal component analysis (PCA) was strategically implemented to address the DARWIN dataset’s high dimensionality (451 features), focusing on spatiotemporal handwriting variables like air_time and paper_time. PCA condensed these into orthogonal components that captured 95% cumulative variance, eliminating redundant kinematic features (eg, overlapping stroke velocity metrics) while preserving discriminative power for AD-related motor-cognitive patterns. The threshold of 95% variance retention was chosen to minimize noise from minor handwriting variations unrelated to neurodegeneration. Prior to PCA, feature filtering removed near-zero variance metrics (<5% unique values) and highly correlated variables (Pearson r>0.9), reducing multicollinearity that could distort component interpretation.

For non-DARWIN datasets with missing values, SMART-Pred uses context-aware imputation: numerical features use median values stratified by diagnostic status to avoid dilution of AD-specific patterns, while categorical variables adopt a hybrid approach-mode replacement for features with <10% missingness and “Missing” flagging for higher rates. This dual strategy ensures robustness across heterogeneous data sources while maintaining compatibility with the tool’s multi-algorithm framework. The preprocessing workflow optimizes computational efficiency without sacrificing clinical interpretability, enabling focused analysis of neurodegeneration-sensitive handwriting biomarkers.

The model training process uses a robust validation strategy involving 10-fold cross-validation repeated 5 times. The system has 10 classic ML algorithms (Table 1). The models range from traditional approaches (eg, logistic regression and naïve Bayes) to advanced ensemble methods (eg, random forest and gradient boosting) and deep learning (eg, neural network), and the selection has been driven by the need to balance algorithmic diversity, clinical utility, and technical robustness. These models have been chosen to cover a broader spectrum of approaches: linear models (eg, logistic regression) provide interpretability for clinical stakeholders, ensemble methods (eg, random forest and AdaBoost) address nonlinear relationships while reducing overfitting, and deep learning models (eg, neural network) capture complex interactions. Criteria, such as accuracy, computational efficiency, and explainability, have guided the selection. Domain-specific validation ensures that the models excel at analyzing temporal handwriting dynamics and mitigates class imbalance. The inclusion of both high-precision neural networks and interpretable models optimizes the tradeoff between complexity and clinical transparency, while cross-validation confirms consistent performance. This multi-algorithm strategy ensures adaptability to diverse patient profiles and aligns with SMART-Pred’s goal of delivering a robust, deployable tool for early AD detection. Detailed information about each algorithm’s implementation and theoretical foundation has been provided previously [25-33]. Hyperparameter optimization is performed through a grid search process to identify the best model configuration.

The evaluation module provides a comprehensive assessment through multiple metrics and visualizations. The system generates validation model performance metrics (Figures 6 and 7), including accuracy [87], sensitivity [88], specificity [88], and F₁-score [89], for model selection; test model performance metrics (Figure 8), including accuracy [34], sensitivity [35], specificity [35], F₁-score [36], and ROC [37], for final evaluation; and ROC curves (Figure 9) for comparing model performance. Additionally, variable importance analysis (Figure 10) is conducted to identify key predictive features across different models. Lastly, SHAP analysis is conducted to interpret the predictions made by the 10 ML classifiers. All evaluation results are presented through interactive visualizations and data frames, allowing the examination of model performance from multiple perspectives.

This study used secondary, deidentified data and therefore did not require Institutional Review Board approval. All data used in this study have been anonymized to protect privacy.

In SMART-Pred, the validation results (Table 2) demonstrated the diverse array of models analyzed, revealing significant variations in performance metrics, such as accuracy, sensitivity, specificity, F₁-score, and area under the curve (AUC), for the DARWIN dataset among the models. The neural network and AdaBoost classifiers emerged as top performers, exhibiting high accuracy scores of 81% and 80%, respectively. Moreover, AdaBoost and neural network achieved commendable AUC scores (92% and 91%, respectively), suggesting a robust capability to distinguish between positive and negative AD cases. Conversely, models, such as k-nearest neighbors (KNN) and naïve Bayes, were noted for lower overall performance, revealing potential limitations in handling the DARWIN dataset’s intricacies.

When the model was used for prediction in the test set (Table 3), the AdaBoost classifier stood out with a remarkable accuracy of 85%, a balanced sensitivity of 88%, an F₁-score of 85%, and an AUC of 92%, illustrating its ability to generalize well beyond the validation dataset. Such consistency between the validation and test phases highlights the robustness of the AdaBoost model for practical applications. The extreme gradient boosting (XGBoost) classifier also demonstrated reliable performance across the dataset, maintaining stable accuracy and specificity, further reinforcing its candidacy for real-world deployment. Many other algorithms in our pipeline, such as the gradient boosting and random forest classifiers, achieved commendable evaluation scores across the evaluation metrics, reaffirming the robustness of the pipeline for classification-based predictive modeling.

On integrating findings from both evaluation phases, it becomes evident that ensemble models (random forest, gradient boosting, AdaBoost, and XGBoost) hold significant promise due to their balanced performance metrics and strong generalization capabilities [90-94]. These models provide a compelling combination of sensitivity and specificity, which is crucial for the diagnostics required in AD detection. The observed fluctuations in the performance of the neural network classifier from validation to testing (especially for recall) suggest that while it possesses inherent strengths, there is room for enhancement.

Our comparative analysis underscores ensemble models (random forest, gradient boosting, AdaBoost, and XGBoost) as the most robust candidates for AD diagnostics in the scope of this work, given their superior performance across both the validation and test datasets [95-98]. These ensemble models have good, balanced accuracy in this regard, making them particularly suited for clinical settings where precise prediction and identification are critical. The insights garnered from this study pave the way for continued exploration into model optimization, potentially enhancing the applicability and accuracy of ML techniques in terms of advancing AD research and the early diagnosis of other diseases, which can be considered crucial in tailoring interventions to target diseases.

Based on the ROC curves (Figure 11), the ensemble models (AdaBoost: AUC=0.92; random forest: AUC=0.89; gradient boosting: AUC=0.89; XGBoost: AUC=0.88) had the strongest performance among the 10 ML models considered in this study. The findings suggest that the AdaBoost ensemble model is highly effective in correctly identifying positive and negative instances for the given classification task. AdaBoost was closely followed by random forest and gradient boosting, both of which demonstrated impressive AUC values of 0.89. The XGBoost and neural network classifiers both achieved an impressive AUC value of 0.88.

In contrast, the decision tree model exhibited the weakest performance, with an AUC of 0.73. While this is still better than random guessing, it suggests that the decision tree algorithm may not be the most suitable choice. The remaining models, including logistic regression, naïve Bayes, SVM, and KNN, had AUC values ranging from 0.78 to 0.83, indicating reasonably good predictive capabilities. The intersecting nature of the ROC curves highlights the better tradeoffs between different models [99-102]. Certain algorithms may excel at specific levels of the false positive rate, which can be an important consideration when selecting the most appropriate model for the task at hand [63].

Building upon our variable importance analysis of SMART-Pred (Figure 12), the partial variable set was constructed by selecting the most influential features among all the algorithms identified through our importance ranking analysis, including “air_time” and “paper_time” variables. Results for the reduced feature model analysis via SMART-Pred are shown in Tables 4 and 5.

The comparative analysis of the reduced feature model and full feature model showed that models trained on the selected partial variables (reduced feature model) consistently demonstrated equal or superior performance compared to those trained on all variables (full feature model), as seen in Tables 4 and 5. The comparison between the full and partial variable sets (reduced feature model) revealed patterns in both validation (Figure 13) and test (Figure 14) metrics.

The pattern was particularly profound for models, such as SVM, naïve Bayes, KNN, and neural network, which showed substantial improvements across all metrics when using the selected important variables (most notable was the neural network’s approximately 20% increment in the reduced feature model’s test recall, from 69% to 88%). Ensemble methods like random forest, gradient boosting, AdaBoost, and XGBoost demonstrated slight improvements in performance across both variable sets, highlighting their inherent robustness regardless of feature selection [103,104]. Notably, the improvements observed in the validation metrics were largely mirrored in the test metrics, indicating that the benefits of using carefully selected important variables generalize well to unseen data.

The consistent enhancement across various performance indicators, including accuracy, recall, precision, F₁-score, and ROC values, in both the validation and test scenarios reinforces the effectiveness of our variable importance–based feature selection approach. These findings strongly validate our strategy of using variable importance ranking for feature selection, demonstrating that focusing on the most influential variables not only maintains or improves model performance but also potentially reduces computational complexity and simplifies the model optimization process [105-108]. In the reduced feature model, the SVM classifier achieved an accuracy of 89% (95% CI 0.77‐0.96) with an AUC of 92%, while the neural network algorithm reached an accuracy of 91% (95% CI 0.79‐0.97) with an AUC of 94%, after identifying the most significant features for AD prediction in the test set. The comparison of ROC curves is presented in Figure 15.

Interpreting the results and understanding the decision-making process of ML models has become paramount, especially in critical fields like medical diagnostics. In the context of AD detection, understanding which features or biological markers most influence a model’s prediction (specifically direction of influence) can provide invaluable insights for medical professionals. In lieu of this, this study performed SHAP analysis. However, for brevity and ease of presentation, the SHAP analysis of the 2 best models (neural network and SVM classifiers) is presented in this section, while the SHAP analysis of the remaining 8 models has been presented in Multimedia Appendix 2.

The SHAP analysis of the neural network classifier indicated that air_time24 and air_time5 (mean SHAP values of −0.0029 and −0.0008, respectively) had the greatest negative influence on AD prediction, while air_time2 and paper_time8 (mean SHAP values of +0.0018 and +0.0012, respectively) had the greatest positive influence on AD prediction (Figure 16A).

For the support vector classifier, paper_time23 and air_time17 (mean SHAP values of −0.0013 and −0.0004, respectively) had the greatest negative influence on AD prediction, while air_time6 and paper_time8 (mean SHAP values of +0.0013 and +0.0009, respectively) had the greatest positive influence on AD prediction (Figure 16B).

AI is transforming medical practice and research by enhancing disease diagnostics, accelerating biomarker discovery, and revolutionizing disease surveillance [109-115]. In diagnostics, AI algorithms can examine complex medical data, such as imaging findings, genetic information, and clinical records, to identify subtle patterns that might be missed by human observers [116-120]. This capability leads to earlier and more accurate disease detection, potentially improving patient outcomes. In biomarker identification, AI’s ability to process vast amounts of multiomic data is uncovering novel indicators of disease presence, progression, and treatment response [121,122]. These AI-discovered biomarkers are paving the way for personalized medicine approaches and more targeted therapeutic interventions. For disease surveillance, AI systems are proving to be invaluable in monitoring and predicting disease outbreaks on a global scale [123]. By analyzing diverse data sources, including social media, environmental factors, and health records, AI can identify emerging health threats in real-time, enabling rapid response and containment strategies [124,125]. Moreover, AI’s impact extends to drug discovery, treatment optimization, and health care resource allocation, promising a future of more efficient, effective, and accessible health care delivery [126,127].

The SMART-Pred application demonstrates a robust, user-friendly, and customizable approach to variable importance analysis across multiple ML models. This innovative tool offers valuable insights into the predictive power of various features in disease diagnostics, biomarker identification, and disease surveillance, particularly in the context of AD, as demonstrated in this study. By using the “varImp()” function and SHP analysis in R in SMART-Pred, our study identified the top-most influential variables for each model, providing a comprehensive view of feature relevance in AD prediction.

A thorough analysis of variable importance across all models revealed consistent patterns and model-specific characteristics. The “air_time” features, particularly air_time23, air_time2, and air_time6, emerged as consistently important variables across multiple models, including naïve Bayes, KNN, AdaBoost, and SVM. Additionally, “paper_time” features (paper_time17 and paper_time23) showed significant importance across several models, indicating the crucial role of temporal features in prediction. The selection of air_time (pen movement duration above paper) and paper_time (pen contact duration) in SMART-Pred’s reduced feature model is rooted in their direct biological ties to AD pathology. Air_time reflects dysfunction of the prefrontal cortex, a region critical for motor planning and task initiation [128,129]. AD-related neurodegeneration is reflected in handwriting performance, with patients showing longer overall writing times and substantially increased air times between pen strokes across everyday copying tasks, indicating hesitation and disrupted sequencing of movements as they struggle to translate cognitive intentions into fluent motor output [130-132]. Paper_time, conversely, correlates with motor execution deficits caused by degeneration of the basal ganglia and cerebellar region, which impairs fine motor control. Quantitative tablet-based studies have reported that kinematic and pressure features, such as time in air, speed, and complexity, can correctly classify healthy controls, patients with mild cognitive impairment, and patients with AD, with roughly 70%-80% accuracy in 3-group models and above 90% accuracy in several pairwise contrasts. However, it was observed that the accuracy of classification was significantly influenced by the characteristics of the groups being categorized and the particular task, with rates varying from 63.5% to 100%. Moreover, the diagnostic accuracy derived from kinematic measurements exhibited higher specificity in differentiating normal cognition from impaired cognition (mild cognitive impairment and AD), whereas enhanced sensitivity was seen in discriminating between the degrees of impaired cognition (mild cognitive impairment vs AD) [133-135]. More recent digital pen work has shown that handwriting characteristics distinguish patients with AD from controls, with the task accuracy of the XGBoost model achieving a maximum value of 96.55% and the AUC reaching up to 99.10%, proving that handwriting characteristic analysis is promising in auxiliary AD screening or AD diagnosis [136]. On the other hand, the spatiotemporal dynamics of simple loop handwriting separate patients with early-stage AD from healthy older adults, with about 74% classification accuracy [137]. These findings support total duration, time in air, and related temporal variability as sensitive quantitative markers that differentiate healthy aging, mild cognitive impairment, and AD and that can contribute to early staging and screening.

The validity of the variables is further supported by multimodal evidence. Neuroimaging and digital clock drawing studies have linked temporal handwriting features, including “time in air” and “time on paper,” to global brain and gray matter volumes, while time-based handwriting metrics have shown significant negative correlations with global cognitive scores, such as the MoCA (Montreal Cognitive Assessment), supporting the interpretation of prolonged air_time and paper_time variability as markers of cognitive decline [138-142]. Compared with invasive biomarkers, such as cerebrospinal fluid Aβ42, which require lumbar puncture and typically achieve diagnostic sensitivities of around 80% at a cost of approximately US $1000 per test [143,144], and FDG-PET (fluorodeoxyglucose positron emission tomography) scans, which show similar median sensitivity but are substantially more expensive (often around US $3000 per scan) [145,146], digital clock drawing metrics, such as air_time and paper_time, provide noninvasive, low-cost screening with high diagnostic accuracy for early cognitive impairment and AD [147], with our SMART-Pred protocol achieving 88% sensitivity at a cost of approximately US $5 per test (our study). Their ability to capture both executive dysfunction (via planning delays) and visuospatial deficits (via erratic stroke execution) provides a holistic view of AD’s cognitive-motor integration breakdown, aligning with National Institutes of Health priorities for functional digital biomarkers [148-150]. This dual focus on mechanistic relevance and clinical practicality makes them ideal for scalable, early AD detection in routine care settings.

Consistent with the literature, our findings showed that random forest had a more balanced feature utilization [151,152], with paper_time6 showing maximum importance (100.00), followed by air_time23 (98.27) and total_time9 (94.82). The model also highlighted the significance of diverse features, such as paper_time23 (90.20), mean_speed_in_air25 (89.03), and mean_jerk_in_air17 (84.03), suggesting a more comprehensive feature integration approach [153-156]. Gradient boosting and XGBoost showed similar patterns but with distinct emphases [156]. Gradient boosting prioritized air_time16 (100.00), while XGBoost highlighted air_time15 (100.00) as the most important feature. The gradient boosting model incorporated additional variables like pressure_mean8 and mean_speed_on_paper2 in the predictions, while the XGBoost model incorporated additional variables like gmrt_in_air1 and total_time3 in the predictions. The neural network model exhibited a unique feature importance pattern, emphasizing variables that were less prominent in other models. While including air_time features, it notably prioritized gmrt_on_paper2 (100.00), mean_acc_in_air13 (98.61), and num_of_pendown19 (98.58), suggesting its ability to capture better patterns in the data, particularly those related to acceleration and movement characteristics. These findings regarding variable importance support the notion that interpretability is crucial in AI systems, especially in medical applications [157-161]. The ability to identify and understand underlying diagnostic biomarkers is not only beneficial for enhancing the diagnostic process but also plays a vital role in tailoring treatment plans for patients [162-168].

ROC curve analysis provided a comparative evaluation of various ML models when assessed with all available variables (full feature model) versus a carefully selected subset of the most important variables (“air_time” and “paper_time” variables; reduced feature model). In the full feature model, AdaBoost demonstrated exceptional predictive capability with an AUC of 0.92, while decision tree showed relatively lower performance with an AUC of 0.73. Strong performance was also noted for random forest and gradient boosting (both with an AUC of 0.89) and XGBoost and neural network (both with an AUC of 0.89). In the reduced feature model, neural network and SVM classifiers outperformed all other algorithms (AUC values of 0.94 and 0.92, respectively), revealing their effectiveness even with fewer inputs. Ensemble models, including random forest, gradient boosting, XGBoost, and AdaBoost, continued to perform well, achieving AUC values ranging from 0.87 to 0.91, which reflect their robustness [169-172]. Interestingly, the decision tree’s AUC improved to 0.81, indicating that it benefited significantly from targeted variable selection in the reduced feature model. Consistent with the literature, our results from the SMART-Pred analysis highlight the consistent strength of ensemble models, such as random forest, gradient boosting, XGBoost, and AdaBoost, across varying variable sets and support the strategic approach of leveraging variable importance ranking to enhance model performance [173-179]. By focusing on critical features, models can maintain or even improve accuracy, as demonstrated in this work. However, it should be emphasized that nothing in this work demonstrated causality between these variables and AD.

SMART-Pred offers a unique approach to AD diagnostics by employing handwriting analysis as a noninvasive biomarker, distinguishing itself from other AI tools in the field. Unlike most existing tools that use cognitive tests, magnetic resonance imaging scans, or blood-based markers, SMART-Pred leverages the DARWIN dataset, which includes handwriting samples from 174 participants (89 patients with AD and 85 healthy controls) across 25 tasks, identifying critical predictors like air_time and paper_time. This focus provides a novel, cost-effective method for early AD detection. The tool integrates 10 diverse ML models, including random forest, AdaBoost, and neural network, within a user-friendly R Shiny application, democratizing access to advanced AI for nonspecialists and enabling robust performance comparison and customization. With neural network achieving 91% accuracy and SVM achieving 89% accuracy on the test set of the reduced feature model, SMART-Pred surpasses many clinical diagnostic tools (typically having around 81% accuracy) using noninvasive data, and its emphasis on interpretability through variable importance ranking (eg, air_time and paper_time) via the “varImp()” function in R aids physician acceptance and hypothesis formulation.

SMART-Pred stands out due to its reliance on accessible handwriting data compared to resource-intensive methods like magnetic resonance imaging scans or genetic testing used by tools, such as the USC model (approximately 85% accuracy) [180] and the Cambridge AI tool (82% accuracy for progression prediction) [45]. While a quantum ML approach has reported an exceptional 99.89% accuracy, its practical application is limited by computational complexity [181]. On the other hand, SMART-Pred prioritizes ease of use and scalability. Unlike the UCSF model, which predicts AD risk up to 7 years in advance using clinical records (72% accuracy), SMART-Pred focuses on immediate diagnostic classification for direct clinical application. Its ability to bridge complex AI algorithms with user-friendly interfaces addresses a critical gap in clinical adoption, and this is further enhanced by its focus on interpretability, a challenge for many AI models. By pinpointing specific handwriting features as predictors, SMART-Pred not only facilitates early detection but also contributes to understanding potential risk factors, paving the way for tailored interventions.

The interplay between AI interpretability and physician acceptance is a key factor in integrating AI systems into health care. SMART-Pred, a multifaceted R Shiny AI-based predictive modeling application, demonstrated robust predictive power in AD diagnosis using the DARWIN dataset. Incorporating 10 ML algorithms with tunable parameters, it achieved optimal results, with ensemble models like random forest and AdaBoost excelling across evaluation metrics. This provides an efficient, customizable approach to AI modeling, particularly for complex datasets and disease diagnosis, which is extendable to other classification-based scenarios. Its ability to identify potential risk factors makes it valuable for guiding hypothesis formulation and experimentation across health care domains. Research indicates that physicians are more likely to adopt AI technologies when the reasoning behind insights is clear, especially in complex fields like AD diagnosis and management [182-184].

Future studies could focus on clinical assessments to evaluate whether top variables like air_time and paper_time are sufficient for AD diagnosis, strengthening the synergy between AI outcomes and experimental findings. Additionally, SMART-Pred could be integrated into electronic health record systems to identify biomarkers of successful aging, enhance disease diagnosis and surveillance, and analyze medical records, addressing public health concerns through data-driven insights and personalized medicine strategies. The use of smart home data for predicting AD symptoms has also shown promise, highlighting the potential of diverse data sources in AD research, with SMART-Pred’s handwriting analysis offering a complementary approach.

SMART-Pred demonstrated competitive performance compared to recent AI models for AD prediction. Its unique use of handwriting analysis and accessibility as an R Shiny application contribute significantly to the field. Future work could also explore integrating multiple data modalities to enhance its predictive accuracy and robustness. Additional clinical research is needed to evaluate the practical applicability of the top-ranked variables (air_time and paper_time) in real-world AD risk assessment and diagnosis.

A comprehensive and comparative analysis of the performance of AI tools for AD detection and prediction is provided in Table 6.

The implementation of SMART-Pred, an AI-based tool for early AD detection via handwriting analysis, holds transformative practical design implications across clinical diagnostics, health care technology, and neurodegenerative research. In clinical settings, SMART-Pred provides a noninvasive, cost-effective screening option, achieving up to 91% accuracy with the neural network model (with 95% CI: 0.79‐0.97 and AUC=94%), which can be seamlessly integrated into primary care where access to advanced neuroimaging or cerebrospinal fluid testing is limited. Using simple handwriting tasks from the DARWIN dataset, the application enables early identification of motor-cognitive decline, potentially reducing diagnostic delays, especially in underserved populations. This supports value-based care by enhancing efficiency and patient outcomes, aligning with broader trends of AI adoption in health care, and prioritizing patients for further evaluation or early interventions.

Beyond clinical use, SMART-Pred influences health care technology by showcasing a user-friendly R Shiny interface that automates complex ML workflows (data preprocessing, model training, and evaluation) for nonspecialist clinical researchers and providers while addressing challenges like infrastructure compatibility and algorithmic bias. Its focus on explainability through feature importance ranking (air_time and paper_time) promotes transparency, building trust among clinicians who are wary of black-box systems. In neurodegenerative research, SMART-Pred inspires exploration of noninvasive biomarkers for other disorders like Parkinson disease and Huntington disease, and future validation on datasets like ADNI could lead to hybrid models combining handwriting with imaging or genetic data for enhanced precision. By prioritizing clinical utility, SMART-Pred supports future AI development in radiology and beyond, encouraging interdisciplinary collaboration and clinician involvement in design to address real-world health care needs and drive innovation in diagnostics.

The SMART-Pred tool has demonstrated promising capabilities for AD prediction through handwriting analysis, but it faces a few critical limitations in its basic version. Computationally, its exclusive reliance on CPU processing within the R environment restricts parallel computing capabilities, leading to inefficiencies when handling large datasets or complex ML algorithms like neural network [190]. This architectural constraint directly impacts scalability, particularly for resource-intensive tasks such as hyperparameter optimization and multimodal data integration. A fundamental reproducibility challenge stems from the inability to save key outputs (model metrics, ROC curves, and trained model states), hindering longitudinal studies and comparative analyses [191-194]. These limitations collectively restrict the tool’s utility in real-world clinical workflows.

To address these issues, the authors propose an advanced version integrating Python-based frameworks like TensorFlow for GPU-accelerated neural network models and enhanced computational efficiency. Planned upgrades include flexible hyperparameter optimization, automated parameter distribution analysis, and comprehensive result-saving functionalities. Future validation will expand beyond the DARWIN dataset to incorporate multimodal data from the ADNI, encompassing neuroimaging, genetic, and biochemical biomarkers. This broader validation aims to assess generalizability across diverse populations and clinical settings while enabling cross-modal biomarker comparisons, a critical step toward establishing SMART-Pred as a clinically actionable tool for early AD detection.

Our study on SMART-Pred aligns with the growing trend of using AI for the early detection and prediction of AD. The performance of our model (91% accuracy with neural network, 95% CI: 0.79‐0.97; AUC=94%) compares favorably with recent advancements in the field. Table 7 presents a concise comparison of studies that used ML, explainable AI, and the DARWIN dataset for AD detection.

The comparative analysis revealed 3 critical insights. First, the studies demonstrate feature consensus, identifying temporal handwriting features like “air_time” as pivotal predictors, thereby validating their biological relevance to AD motor-cognitive decline through their association with prefrontal cortex dysfunction and motor planning deficits. Second, SMART-Pred represents a methodological evolution from prior work by expanding model diversity (10 algorithms vs up to a maximum of 7 algorithms in earlier studies), incorporating neural networks to capture complex nonlinear patterns in handwriting dynamics, and advancing biomarker identification through dual focus on “air_time” (in-air movement duration) and “paper_time” (pen contact duration) rather than single-feature analysis. Third, despite architectural differences, SMART-Pred classifiers performed very well (with neural network achieving an accuracy of 91% [95% CI 0.79-0.97]), highlighting the DARWIN dataset’s robustness for handwriting-based diagnosis while indicating that model selection impacts biomarker discovery more than absolute accuracy in this domain. This progression from single-feature interpretation to multi-algorithm, multibiomarker analysis reflects an intentional shift toward clinical translatability, balancing explainability with predictive power.

The SMART-Pred R Shiny application represents a significant advancement in AI-based predictive modeling for medical diagnostics, offering a user-friendly interface and comprehensive algorithm selection. This tool holds value for researchers and clinicians in personalized medicine and public health surveillance, demonstrating potential to enhance early detection and screening strategies for conditions such as AD and Parkinson disease. By bridging the gap between computational modeling and clinical application, SMART-Pred exemplifies the growing trend of leveraging interactive data visualization and AI-powered analysis in health care settings.

Future development of SMART-Pred will focus on clinical validation and address the challenges associated with imbalanced datasets. The roadmap includes expanding algorithmic support to encompass advanced ML techniques, image recognition architectures, and analysis capabilities for diverse data types such as text, time series, and graph data. Additionally, plans to improve visualization capabilities and user interface design aim to increase accessibility and power. These ongoing enhancements are designed to create a more flexible and comprehensive platform for data analysis across various scientific domains, solidifying SMART-Pred’s role in advancing predictive modeling in health care and beyond.