The goal of this clinical trial is to test the feasibility and effectiveness of transcutaneous vagus nerve stimulation (tVNS) to the ear on pain and autonomic function in people with knee osteoarthritis (OA). The main questions it aims to answer are: 1) whether tVNS is feasible to be used in people with knee OA; 2) whether tVNS demonstrates the trend in improving knee pain; and 3) whether tVNS has physiological effects on autonomic function (e.g., parasympathetic function) and pain perception in the central nervous system such as brain (i.e., central pain mechanisms). Participants will be asked to complete a battery of self-reported questionnaires about their demographic and behavioral information, ethnicity, pain, sleep, psychological/emotional symptoms. Subsequently, participants will complete baseline assessment where investigators will assess their knee pain severity, central pain sensitivity, and heart rate variability (a measurement for autonomic function). Then participants will receive a 60-minute tVNS. Investigators will redo the same assessment as baseline assessment after tVNS intervention to see the degree of knee pain, central pain sensitivity, and autonomic function changes. At the end of the study, investigators will assess their satisfaction level with the tVNS intervention and the feasibility of the intervention (e.g., completion rate, side effects).
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Change in Pressure Pain Threshold
Timeframe: Same day assessment with 3 data points: baseline, immediately after- and 15 minutes after tVNS intervention
Change in Conditioned Pain Modulation
Timeframe: Same day assessment with 3 data points: baseline, immediately after- and 15 minutes after tVNS intervention
Change in Temporal Summation
Timeframe: Same day assessment with 3 data points: baseline, immediately after- and 15 minutes after tVNS intervention
Change in Parasympathetic Function
Timeframe: Same day assessment with 3 data points: baseline, immediately after- and 15 minutes after tVNS intervention
Change in knee pain
Timeframe: Same day assessment with 3 data points: baseline, immediately after- and 15 minutes after tVNS intervention
Change in and The Western Ontario McMaster Universities Osteoarthritis Index
Timeframe: Same day assessment with 3 data points: baseline, immediately after- and 15 minutes after tVNS intervention
Safety about tVNS intervention
Timeframe: At the end of the study visit
Satisfaction Level
Timeframe: At the end of the study visit