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S.1.02 Novel accelerometer data processing methods for quantifying movement behaviors in free living environments

Tracks
Room: Hunua #2 Level 1
Thursday, June 18, 2020
8:30 AM - 9:45 AM
Hunua #2 Level 1

Details

Purpose: This symposium will focus on the application of advanced accelerometer data processing methodologies for human activity recognition with an emphasis on monitoring movement behaviours in true free living scenarios. Rationale: Accelerometer-based monitoring of movement behaviours has become popular among researchers and consumers. However, the research potential of accelerometers has been severely under-utilised, with analysis restricted to the application of simple cut-points methods. Machine learning (ML) approaches to accelerometer data reduction have emerged as a more accurate and versatile alternative to cut-points; however, most models have been developed in the laboratory using structured activity trials. Validating models in the laboratory is unrealistic because only a limited number of activities are included; and fixed duration activity trials fail to replicate the episodic nature of movement behaviours over a 24 hour cycle. If ML approaches are to be implemented in free-living studies, it is critically important to evaluate the performance of activity classification models in new data and/or different population groups under true free-living conditions. Objectives: · To increase knowledge of ML approaches to accelerometer data processing. · To highlight the performance differential between models trained using data collected in controlled laboratory environments and models trained on free living data. · To provide guidance on the implementation of classification algorithms in free living studies involving pre-schoolers, school-aged youth, and adults with chronic health conditions. · To identify current gaps in knowledge and future research priorities. Summary: The symposium will focus on the challenges associated with developing ML activity classification models for free living environments. The three presenters will address the topic in a different study population – pre-schoolers, school-aged youth, and adults with a chronic health condition. The similarities and differences in findings will be highlighted and discussed. Format Chair: Introduction and rationale (Stewart Trost) – 10 minutes Oral 1: Evaluation and comparison of laboratory-based and free-living activity recognition models for preschool-aged children under free-living conditions (Matthew Ahmadi) – 15 minutes (10 + 5) Oral 2: Activity classification models for children: how well do lab-developed models generalise to free-living conditions? (Tom Stewart) - 15 minutes (10 + 5) Oral 3: Can free-living activity classification models developed in healthy adults be used in a dialysis patient population? (Rosemary Walmsley) – 15 minutes (10 + 5) Discussant: Wrap up (Scott Duncan) – 5 minutes Panel questions and guided discussion (Scott Duncan) – 15 minutes


Speaker

Mr. Matthew Ahmadi

Evaluation and comparison of laboratory-based and free-living activity recognition models for preschool-aged children under free-living conditions

Abstract

Machine learning activity recognition models provide researchers with alternative activity metrics in addition to intensity. However, existing algorithms for preschool children have been trained on data from laboratory-based activity trials and their performance has not been investigated under free-living conditions.

Purpose:  To evaluate the accuracy of laboratory trained hip and wrist Random Forest (RF) classifiers for automatic recognition of five activity classes: sedentary, light household activities and games, moderate-to-vigorous sports and games, walking, and running in preschool children under free-living conditions. In addition, the performance of the laboratory trained models was benchmarked against models trained on free-living data.

Methods:  31 children (4.0 ± 0.9 yrs) were video recorded using a GoPro during a 20-minute unstructured active play session. Participants wore an ActiGraph GT3X+ on their right hip and non-dominant wrist. A bespoke two-stage direct observation scheme was used to continuously code ground truth activity class, and to identify which movement behaviours contributed to misclassification errors, the specific activity types occurring within each class.

Twenty-one of the children were randomly selected to train free-living RF classifiers for the hip and wrist. Performance of the laboratory and free-living classifiers was subsequently assessed in the hold-out ten children by calculating overall recognition accuracy, kappa statistics, and generating confusion matrices summarising class level accuracy.

Results:  Accuracy for the hip and wrist laboratory trained RF classifiers was 67.5% (κ = 0.42) and 56.9% (κ = 0.32) respectively. In comparison, accuracy for the free-living trained hip and wrist RF classifiers was 83.1% (κ = 0.70) and 79.7% (κ = 0.64), respectively. The free-living RF classifiers provided substantial improvement for classification of sedentary (5.6% - 11.3%), light household activities and games (10.2% - 26.7%), walking (43.5% - 65.0%) and running (16.6% - 22.2%).

Conclusions:  Laboratory trained activity recognition models for preschool aged children do not perform well when implemented in new data collected under true free-living conditions. In contrast, classifiers trained on free living data perform well.  These findings support the view that machine learning activity recognition models be trained under free-living conditions.

Dr Tom Stewart
Research Fellow
AUT University

Activity classification models for children: how well do lab-developed models generalise to free-living conditions?

Abstract

Purpose: Classification of activity behaviours using raw accelerometer data is becoming more prominent. Almost all activity classification algorithms are developed using data collected in controlled laboratory environments which may not be generalisable to free-living settings. This study examined how machine learning models trained on laboratory data performed in free-living settings, and how the accuracy changed when the models were retrained with additional free-living data.

Methods: In a lab setting 40 children (19 males, aged 10.1 ± 1.7 years) were equipped with two Axivity AX3 accelerometers worn on their thigh and lower back. They performed a series of activities (e.g., sitting, standing, walking, running, lying) that were captured by video camera (criterion measure). Fifteen new children (10 male, aged 10.0 ± 2.6) wore the same two accelerometers and a small wearable video camera that captured their free-living movement behaviours.

Using the lab dataset, a random forest was trained to classify each activity using several features of the accelerometer data (e.g. axis means). After this model was evaluated in the lab setting, it was used to predict activity type in the free-living dataset. As a last step, the model was retrained with both the lab and free-living data together, and the accuracy was estimated using leave-one-subject-out-cross validation.

Results: The accuracy of the lab-trained model was 97.8% (95% CI: 97.6–98), kappa κ = 0.98. This dropped to 92% (91.6–92.5), κ = 0.88, when applied to the free-living data. Retraining the model with additional free-living data improved the free-living accuracy to 97.2% (97–97.4), κ = 0.96.

Conclusions: Activity classification models developed in a laboratory setting showed a ~6% reduction in accuracy (10% reduction in κ) when applied in a free living setting. Accuracy improved when models were retrained with additional free-living data. Future studies should include free-living data when developing classification models to ensure their generalisability.

Ms Rosemary Walmsley
Phd Student
University Of Oxford

Can free-living activity classification models developed in healthy adults be used in a dialysis patient population?

Abstract

Purpose: Machine learned (ML) models developed to classify activity behaviours from raw accelerometer data in free-living were shown to be accurate (82.7%, kappa κ=0.74) and demonstrated epidemiological utility in over 90,000 UK Biobank participants. However, it is unknown how well these ML models generalise to inactive diseased populations. We therefore examined if ML models trained on free-living data from healthy adults could be used in a dialysis patient population.

Methods: 153 healthy UK adults were asked to wear an Axivity AX3 accelerometer on the dominant wrist for 24 hours and a Vicon Autographer wearable camera to capture their free-living movement behaviours. In a separate study, 25 adults with end-stage kidney disease on maintenance dialysis were asked to undergo the same accelerometer and wearable camera protocol. Camera data was labelled by trained annotators into four classes: sedentary behaviour, light tasks, moderate activity, and walking.

Random Forest models were trained to classify activity type from 132 time and frequency domain features for each 30 second epoch, with a Hidden Markov model used to smooth predictions. The models developed in healthy adults were then applied to data from dialysis patients. Models were then retrained using dialysis patients’ data only. Finally, models were retrained with a mix of healthy and dialysis patient data together.

ResultsWhen the model trained in healthy adults was applied to dialysis patients, accuracy was 74.3% (κ=0.16). When trained in dialysis patients only, models achieved accuracy of 72.5% (κ=0.19). When trained in healthy adults and dialysis patients, models achieved accuracy of 74.4% (κ=0.15) on dialysis patients only. 

Conclusions: Activity classification models developed in a healthy population achieved substantially lower accuracy and kappa statistics when applied to a highly inactive dialysis population. While retraining with data from dialysis patients improved the kappa statistics, classification performance remained much lower than in the healthy population. Future studies should be aware of population-specific challenges in machine-learned activity classification, and where possible collect relevant training and validation data in the disease populations of interest. 

 


Chair

Stewart Trost
Associate Director Ihbi
Queensland University Of Technology


Discussant

Scott Duncan
Associate Professor
Auckland University Of Technology

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