Could a High-Fat diet reset energy in long COVID?
NCT ID NCT07745699
First seen Aug 04, 2026 · Last updated Aug 07, 2026 · Updated 3 times
Summary
This trial tests whether a 12-week ketogenic diet program, delivered entirely online, is practical and acceptable for adults with Long COVID who also have ME/CFS and dysautonomia. Participants follow a low-carb, high-fat diet with vitamin B1 and electrolyte support, plus weekly virtual nutrition coaching. The study tracks adherence, safety, and satisfaction, and also measures changes in fatigue, sleep, mood, and daily functioning. The goal is to see if this remote approach could be a viable way to ease symptoms and improve quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ketogenic metabolic therapy (a low-carb, high-fat diet with vitamin B1 and electrolyte support, delivered via telehealth)
- What this could lead to
- If successful, this could point toward a practical, home-based dietary approach to ease fatigue and autonomic symptoms in Long COVID, potentially improving daily functioning and quality of life.
- What could go wrong
- This is a small feasibility study with only 11 participants, so results may not apply broadly. The diet is restrictive and may be hard to follow, and benefits are not guaranteed.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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11 people
The number who actually took part.
- Started
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Dec 2024
- Finished
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Jun 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Age 18 years or older English-speaking Suspected, probable, or confirmed SARS-CoV-2 infection as defined by the Pan American Health Organization Long COVID diagnosed via structured clinical interview, consistent with the World Health Organization clinical case definition and the National Academies of Sciences, Engineering, and Medicine (2024) definition Physician-confirmed diagnosis of post-infectious dysautonomia and ME/CFS; OR self-reported dysautonomia symptoms with a Malmö POTS Score Assessment (MAPS) score greater than 40 Met the National Academy of Medicine diagnostic criteria for ME/CFS Exclusion Criteria: * Known pregnancy or planning pregnancy during the study period Active cancer diagnosis Renal or liver failure Pancreatitis Atrial fibrillation or significant cardiac arrhythmia Significant atherosclerotic disease Uncontrolled hypertension or hypertriglyceridemia Active or recent thrombosis Use of antiepileptic medications Use of SGLT-2 inhibitors Substance use disorder Type I diabetes History of inborn errors of metabolism Previous completion of a nutritional and lifestyle program for this condition
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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National University of Natural Medicine
Portland, Oregon, 97229, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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