Effects of Osteopathic Manipulative Therapy on Long COVID symptoms
Official title: Osteopathic Manipulative Therapy(OMT) Effects on Post-Acute Sequalae of COVID-19(PASC)
Run by University of Louisville · NCT06883513 · Data updated 2026-11-12
This study is testing whether Osteopathic Manipulative Therapy can help people with Long COVID feel better by reducing their symptoms over eight weeks.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 20 (estimated) |
| Sponsor | University of Louisville Academic / other |
| Locations | 1 site (Louisville, Kentucky) |
| Status | Recruiting |
| Started | May 1, 2025 |
| Main results expected | July 3, 2025 |
| Study ends | July 3, 2025 |
| Registry record updated | March 19, 2025 |
| Trial ID | NCT06883513 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals who have tested positive for SARS-CoV-2 at least 6 weeks prior and are experiencing persistent Long COVID symptoms affecting their daily life.
✕Probably not a fit
Patients who do not have a history of COVID-19 or those whose symptoms have resolved may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the impact of Osteopathic Manipulative Therapy (OMT) on individuals suffering from Long COVID, specifically focusing on whether OMT can alleviate various symptoms beyond olfactory dysfunction. Participants will complete digital surveys regarding their symptoms over an 8-week period, receiving either OMT or a placebo treatment. The study aims to determine if multiple OMT sessions yield greater improvements compared to a single session. The research builds on previous pilot data that indicated OMT may improve smell in Long COVID patients.
Why it matters
Potential benefit: If successful, this treatment could provide a non-pharmacological option for alleviating a range of Long COVID symptoms.
How similar studies have gone: Previous studies have shown promising results for OMT in treating specific Long COVID symptoms, but this approach is still being explored for broader symptom relief.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * \- Individuals must claim they have had a prior positive SARS-CoV-2 test at least 6-weeks before the consenting process to proceed with the study * Individuals must claim they have at least one of the following symptoms greater than 6-weeks post infection that is affecting their daily life(these symptoms correlate with the SBQ™-LC): Symptoms of Long Covid Inclusion Criteria: * Shortness of breath or Difficulty Breathing * Difficulty with Movement (balance or tremor) * Muscle Pain or stiffness * Changes in sexual desire * Worsening Generalized Pain * Difficulty with Sleep * Changes in Mood (anxiety or depression) * Changes in Erectile function (Biological males only) * Palpations (irregular heart beats) * Altered Taste * Changes in your Hair * Changes in urination * Dizziness * Altered Smell * Changes in Skin * Changes in bowels * Fatigue * Indigestion * Dry or irritated eyes * Changes in sweating * Difficulty with Cognition (memory or thinking) * Stomach Pain * Changes in menstruation (Biological females only) * Chills or shivering Exclusion Criteria: * If anyone denies they have any of the above symptoms before consent, they will be excluded from the trial * They will also be excluded from the trial if they have suffered any fractured bones in the last 3 months (this will further decrease risk to the patient as the patient will be moved by the physician during the treatment protocol) * Participants who are enrolled in other Long-COVID trials that have an intervention during their participation in this trial will be excluded. However, if they have a history of enrollment in a long-covid trial that has no interventions during this trial, they will not be excluded based on their history of acquiring experimental treatment.
Where it's running
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University of Louisville Outpatient Care Center
Louisville, Kentucky, United States Recruiting
Study contacts
- Principal investigator: Darryl Kaelin, MD, Medical Doctorate (US) — University of Louisville School of Medicine Chair of PM&R Division of the Department of Neurological Surgery
- Study coordinator: Michael E Stenta, DO, Doctor of Osteopathic Medicine
- Email: michael.stenta@uoflhealth.org
- Phone: 15137289344
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Magnetic resonance and rapid brain stimulation for Long COVID cognitive and mood symptoms
This trial will test whether an accelerated outpatient magnetic brain stimulation (iTBS) can help reduce brain fog, depression, and anxiety in adults with Long COVID.
-
Immunoadsorption blood filter for autoimmune long COVID
We will test a blood-filter treatment called immunoadsorption in people with long COVID who have specific autoantibodies to see if their fatigue and daily functioning get better.
-
Anktiva for treating Long COVID symptoms
This will test whether Anktiva helps adults aged 18–69 who had confirmed COVID-19 and now have persistent or worsened Long COVID symptoms.
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Analyzing MicroRNAs and Vitamin B12 in Long COVID Patients with Neurological Symptoms
This study is testing if changes in certain microRNAs and vitamin B12 levels in the blood can help understand and treat neurological symptoms like depression and fatigue in people who have long COVID.
-
Improving life for patients with chronic fatigue syndrome
This study is testing if two medications can help people aged 18-65 with chronic fatigue syndrome feel better and manage their symptoms.
-
Whole-body Cryotherapy for Fatigue in ME/CFS, Fibromyalgia, Long COVID
This study tests whether brief, repeated exposure to extreme cold can help reduce fatigue and related symptoms in adults with ME/CFS, fibromyalgia, or Long COVID compared to healthy controls.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.