Bachelor's Thesis: System and Methods to Determine ME/CFS & Long COVID Disease Severity Using Wearable Sensor & Survey Data
This post is an introduction to my bachelor's thesis background information, related work done before writing the final thesis. The results of this study are included in the final thesis, if you want to read about it, visit this page (opens in a new tab).
The University of Utah
The research project I'm in is a joint study between the University of Utah and the Bateman Horne Center and I am using this project as my bachelor's thesis under Dr. Shad Roundy (opens in a new tab)'s supervision and co-advised by Dr. Tucker Hermans (opens in a new tab).
The purpose of this research project is to find and prove digital bio-marker(s) that can be used to diagnose and measure the severity of myalgic encephalomyelitis/chronic fatigue syndrome (opens in a new tab) (ME/CFS) and Long COVID.
Before I join this study, Turner Palombo (opens in a new tab) already did his master's thesis titled "Development of an Inertial Measurement-Based Assessment of Disease Severity in Chronic Fatigue Syndrome (opens in a new tab)"  and a large portion of my work is based on his.
Originally, I am doing this research project just for fun as a research assistant, but further into the study, I found the project quite interesting and useful, so I decided to use this project for my senior thesis instead of doing a capstone project.
If you don't know what ME/CFS is, CDC has a pretty good overview (opens in a new tab) of it.
Based on a research paper published in 2013 (opens in a new tab) that discusses how the severity of ME/CFS is measured:
CFS symptom severity score: The CFS Severity Score was a self-administered, recall-biased assessment of overall complaints for the previous 6 month period. Fatigue and the 8 minor criteria were scored as none (score = 0), trivial (score = 1), mild (score = 2), moderate (score = 3) and severe (score = 4). 
The method discussed in the paper is still a mainstream method to measure the severity of ME/CFS, but it is relying on patients' subjective, unreliable self-reporting, which is not ideal for medical diagnosis.
If you don't know what Long COVID is, this article (opens in a new tab) from CDC is a good overview of it.
In a recent post (opens in a new tab) (August 8, 2022) published by the National Institute of Health, they mentioned:
In 2015, researchers estimated that ME/CFS affected between 900,000 and 2.5 million people in the United States, most of them undiagnosed. Other symptoms include sleeping issues, problems with memory and cognition, and muscle soreness.
If these symptoms sound familiar, it is because ME/CFS shares symptoms in common with long COVID, a group of symptoms some people who have had COVID-19 experience for weeks or months after their initial illness. Symptoms of long COVID include fatigue, post-exertional malaise, breathing problems, and heart palpitations.
Also, in multiple other studies in symptomatology relating with ME/CFS and Long COVID  (keyword: "ME/CFS", "Long COVID", "Post-COVID CFS", "Symptomatology"), researchers found that the symptoms of ME/CFS and Long COVID are very similar.
Since ME/CFS and Long COVID share multiple similar syndromes, it is reasonable to assume that the same digital bio-marker(s) can be used to diagnose and measure the severity of both diseases.
In Upright Activity and Exercise Intolerance: Critical Concepts in the Evaluation of Chronic Fatigue (opens in a new tab), and also in Clinically accessible tools for documenting the impact of orthostatic intolerance on symptoms and function in ME/CFS (opens in a new tab), the researchers mentioned Orthostatic Intolerance (OI) is correlated with the severity of ME/CFS and Long COVID, and patients' HUA can be statistically quantified with UpTime (but what is UpTime? we define UpTime as the time when the patient's lower leg, the lower part of the leg from the knee to the ankle, is in an upright position).
UpTime definition, screenshot taken from a slide for initial study's presentation
To measure UpTime, we use wearable devices to gather sensor data (accelerometer, gyroscope) and calculate leg angles using Kalman Filtered data points and quaternion, then for each calculated angle, we compare it with a threshold angle (in this case, 39 degrees, see Turner's thesis (opens in a new tab)) to determine if the leg is in an upright position or not.
Since OI refers to the inability to remain upright, with common symptoms such as lightheadedness, and UpTime is measuring patients' HUA, we have high confidence that patients' severe OI would have less HUA thus lower UpTime percentage, thus UpTime is a good candidate to be an objective measure of OI then infers the severity of patients' ME/CFS and Long COVID.
Moreover, since we will already be collecting patients' UpTime data through raw sensor data, why not explore other potential digital bio-markers that can be used to diagnose and measure the severity of ME/CFS and Long COVID? Since people's daily activity level is somewhat related to the steps they take, StepsPerDay is used as a companion digital bio-marker to UpTime.
Even though we're confident UpTime can be a valid digital-biomarker to measure severity of ME/CFS and Long COVID, we still need to prove that through data and evidence.
In an initial study undertaken by Turner Palombo showed a correlation between UpTime and ME/CFS disease severity. However, this result is preliminary as the study that showed the correlation only had 15 subjects. Therefore, we are collaborating with the Bateman Horne Center on a larger study (the ongoing study) with 75 participants which has a ME/CFS cohort, a Long COVID cohort, and a healthy control cohort.
The first objective of this ongoing study will be to verify the finding from the preliminary study. Second we will evaluate UpTime and StepsPerDay as measures of disease severity for ME/CFS and Long COVID. Finally we will explore other potential biomarkers.
I mentioned we used wearable devices to gather accelerometer and gyroscope data, and those data points are coming from IMUs (Inertial Measurement Units).
In the original study, Turner analyzed sensor data generated by Shimmer (opens in a new tab), when I got my hand on the project, we switched to MMS (opens in a new tab), the sensor data format generated by the above two sensors is the same.
Shimmer 3 IMUs on both legs, screenshot taken from a slide for initial study's presentation
The main reason for the switch is due to battery life and participants' comfortness: Shimmer IMUs are big but they only last around 3 days, we found it not ideal for mid-term monitoring (which usually lasts about 1 week), so we switched to MMS IMUs (lightweight, water-proof with our band), which can last up to 2 weeks with our data collection parameters.
MMS IMUs setup
The nice thing about MMS is that they provide very comprehensive APIs for almost all mainstream programming languages and user platforms, I extended their C++ and Python library to allow us to have concurrent serial data transfer from the sensor to Raspberry Pi (or any other Linux-based system).
For each study participant, they will wear the MMS device on one of their lower leg for a week, and send the device back to BHC for data collection through a terminal interface on Raspberry Pi. In addition to wearing the IMUs for a week, participants in the study completed questionnaires including RAND36, OISA, and OIDAS.
All code used for the study will be available as artifacts after our study result is published, and overall workflow is on this simple data flow diagram.
|----------------------------| issue download command |--------| | Terminal (deployed at BHC) | -----------------------> | AWS S3 | |----------------------------| |--------| | |-> watcher | | | |<----------| no change | | change detected | | |--------------| | |----- | preprocessor | <----------- | |--------------| | |--------------------> download | unzip | trim | error check | uptime | steps | notify investigator <--------------| processed data
After study participants send back the MMS device, the data will be downloaded from the device on a Raspberry Pi, compressed, then uploaded to AWS S3. A "watcher" (a cron-job running on local server keeps checking AWS S3 bucket directory) will be triggered to check if there is any new data, if there is, the preprocessor will be triggered to process the data, and finally the processed data will be sent to the investigator.
For data security, the raw sensor data transported from Terminal and AWS S3 (Python Boto3), from AWS S3 to the processing server (Python Boto3) is encrypted with TLS, and data backed up on AWS S3 have AWS-managed encryption with encryption key rotation. Other than that, all data is transported within a local network formed between Tailscale (opens in a new tab) nodes.
Since we collect both accelerometer and gyroscope data at 25Hz for a week for each study participant (~2.5GB per recording session), it would be a waste just to use such comprehensive data to calculate UpTime. So we added StepsPerDay as another digital bio-marker, not quite proven yet, but it is a good candidate (ME/CFS or Long COVID -> possible Orthostatic Intolerance -> not as active -> low step count).
UpTime and StepsPerDay are the two digital bio-markers that are being analyzed now. Methods used are described in Turner's thesis (opens in a new tab). I was able to replicate Turner's results using the same methods in Python (his original code is in MATLAB).
Other than UpTime and StepsPerDay, we also have standardized survey data for each participant (RAND36, OISA, OIDAS, etc.), we are also working on a way (linear/quadratic regression, unsupervised ML, etc.) to combine those data with UpTime and StepsPerDay to get a more accurate diagnosis.
2021-08 ~ 2022-07
- MMS and Raspberry Pi setup
- MMS hardware interface with Raspberry Pi
- Custom library for our specific use case
- Pre-processing pipeline
- UpTime and StepsPerDay calculation
2022-08 ~ 2022-12
- Does UpTime predicts the existence of ME/CFS?
- Does UpTime predicts the existence of Long COVID?
- Does StepsPerDay predicts the existence of ME/CFS?
- Does StepsPerDay predicts the existence of Long COVID?
- Check standardized survey data's correlation with UpTime and StepsPerDay (RAND36, OISA, OIDAS)
2022-12 ~ 2022-05
- Explore multi-regression models
- Explore other digital bio-markers
- Explore ML approach
A meeting note laying out my current research roadmap
After gathering terabytes worth of sensor data, we used the raw data to determine UpTime and StepsPerDay, then evaluate UpTime and StepsPerDay and linear combination of the two as a predictor for ME/CFS disease severity. The final step of our analysis will seek to find a more accurate predictor of ME/CFS disease severity using the data in these questionnaires. We will pursue multi-linear and polynomial regression and an unsupervised machine learning approach to find a classifier for ME/CFS disease severity.
Results of this research are included in the final thesis, if you want to read about it, visit this page (opens in a new tab).
 Palombo T, Vernon S, Roundy S. Development of an Inertial Measurement-Based Assessment of Disease Severity in Chronic Fatigue Syndrome. Master's Thesis, The University of Utah Department of Mechanical Engineering, August 2020.
 Baraniuk JN, Adewuyi O, Merck SJ, Ali M, Ravindran MK, Timbol CR, Rayhan R, Zheng Y, Le U, Esteitie R, Petrie KN. A Chronic Fatigue Syndrome (CFS) severity score based on case designation criteria. Am J Transl Res. 2013;5(1):53-68. Epub 2013 Jan 21. PMID: 23390566; PMCID: PMC3560481.
 Wong TL, Weitzer DJ. Long COVID and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS)-A Systemic Review and Comparison of Clinical Presentation and Symptomatology. Medicina (Kaunas). 2021 Apr 26;57(5):418. doi: 10.3390/medicina57050418. PMID: 33925784; PMCID: PMC8145228.
 Lee, Jihyun et al. ‘Clinically Accessible Tools for Documenting the Impact of Orthostatic Intolerance on Symptoms and Function in ME/CFS’. 1 Jan. 2020 : 257 – 263.
 Stewart JM. Common syndromes of orthostatic intolerance. Pediatrics. 2013 May;131(5):968-80. doi: 10.1542/peds.2012-2610. Epub 2013 Apr 8. PMID: 23569093; PMCID: PMC3639459.