Anti-inflammatory Actions of Osteopathic Manipulative Treatment (OMT_taVNS)
Inflammation
About this trial
This is an interventional basic science trial for Inflammation focused on measuring osteopathic manipulative treatment, transcutaneous auricular vagus nerve stimulation, cytokines, immune cells, parasympathetic nervous system, heart rate variability
Eligibility Criteria
Inclusion Criteria:
- Age of 18 year or above.
Exclusion Criteria:
- Age under 18 years
- Pregnancy
- Any findings on the osteopathic screening/evaluation that would hinder the effectiveness - of the occipito-atlantal decompression or splenic lymphatic pump technique
- Any medication that interferes with the autonomic nervous system function or the immune system (e.g., beta-blockers, steroids, TNF-α inhibitors)
- Any medical condition that affects the autonomic nervous system or the immune system (e.g., splenomegaly, Epstein-Barr infection within the last 6 months, autonomic neuropathy, pure autonomic failure, rheumatic or autoimmune diseases, acquired autoimmune deficiency syndrome)
- Any chronic diseases, such as diabetes and hypertension
- Current drug or alcohol abuse.
Sites / Locations
- Burrell College of Osteopathic MedicineRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
No Intervention
Osteopathic Manipulative Treatment (OMT)
Transcutaneous Auricular Vagus Nerve Stimulation (taVNS)
Time Control
In 4 randomized study sessions, combinations of two different osteopathic manipulative treatment (OMT) techniques (occipito-atlantal decompression [OA DC] and splenic lymphatic pump technique [SpLPT]) or their respective sham interventions will be performed. The 4 study sessions are at least one month apart and consist of 3 consecutive study days on which the same combination of OMT techniques or sham interventions will be performed.
In 4 randomized study sessions, combinations of non-invasive transcutaneous auricular vagus nerve stimulation (taVNS), osteopathic splenic lymphatic pump technique (SpLPT) or their respective sham interventions will be performed. The 4 study sessions are at least one month apart and consist of 3 consecutive study days on which the same combination of taVNS, SpLPT, or sham interventions will be performed.
In 4 study sessions, no intervention will be performed. As with the two experimental arms, the 4 study sessions are at least one month apart and consist of 3 consecutive study days on which no intervention will be performed. This arm serves as a time control group.