Introduction: With advancements in personalised medicine, healthcare delivery systems have moved away from the one-size-fits-all approach, towards tailored treatments that meet the needs of individuals and specific subgroups. As nearly one-third of those diagnosed with epilepsy are classed as refractory and are resistant to antiepileptic medication, there is need for a personalised method of detecting epileptic seizures. Epidemiological studies show that up to 91% of those diagnosed identify one or more epilepsy related trigger as the causation behind their seizure onset. These triggers are person-specific and affect those diagnosed in different ways dependent on their idiosyncratic tolerance and threshold levels. Whilst these triggers are known to induce seizure onset, only a few studies have even considered their use as a preventive component, and whether they could be used as an additional sensing modality for non-EEG detection mechanisms. Objectives: 1. To record person-specific triggers (PST) from participants using IoT-enabled sensors and smart devices. 2. To train and test several dedicated machine learning models using a single participants data, 3. To conduct a comparative analysis and evaluate the performance of each model, 4. Formulate a conclusion as to whether PST could be used to improve on current methods of non-EEG seizure detection. Methodology: This study uses a precision approach combined with machine learning, to train and test several dedicated algorithms that can predict epileptic seizures. Each model is designed for a single participant, enabling a personalised method of classification unseen in non-EEG detection research. Results: Our results show accuracy, sensitivity, and specificity scores of 94.73%, 96.90% and 93.33% for participant 1 and 96.87%, 96.96% and 96.77% for participant 2, respectively. Conclusion: To conclude, this preliminary study has observed a noticeable correlation between the documented triggers and each participants seizure onset, indicating that PST have the potential to be used as an additional non-EEG sensing modality when classifying epileptic seizures.