Can computer games clear the fog? new study tests brain training for ME/CFS
NCT ID NCT07523113
First seen Jun 24, 2026 · Last updated Aug 14, 2026 · Updated 2 times
Summary
This study compares two brain-training programs for adults with ME/CFS who experience brain fog. Both programs include computer games and a mild nerve stimulation device, but one focuses on processing speed and daily tasks while the other emphasizes relaxation and healthy habits. Thirty participants will train remotely over 2-4 weeks and be followed for 6 months to see if their thinking and daily activities improve.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- brain training (computer games and lifestyle coaching) plus non-invasive vagus nerve stimulation
- What this could lead to
- If it works, this could point toward a practical, at-home way to reduce brain fog and improve daily functioning for people with ME/CFS.
- What could go wrong
- This is a very small, early-stage study with only 30 participants. The two approaches are compared head-to-head, so neither may prove clearly better. Results may not apply to everyone with brain fog.
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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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Jun 2028
An estimate. End dates often move.
- 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.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * diagnosis of ME/CFS that preceded cognitive complaints * mild or greater cognitive impairment * moderate or greater brain fog * some impairment in the performance of daily activities * ≥ 18 years, no upper limit if medically stable * reside in the community (as opposed to a hospital or skilled nursing facility) * able to travel to the laboratory on multiple occasions * has Internet service * has a personal computer, laptop, or tablet that can access the Internet * sufficiently fit, from both a physical and mental health perspective, to take part in the study * adequate sight and hearing to complete the UFOV test * adequate thinking skills, e.g., ability to follow directions and retain information to complete UFOV and CTAL, as marked by the judgement of the screener that the candidate is able to adequately complete the UFOV and CTAL * sufficient English proficiency (i.e., ability to speak, understand, read, and write to take part in study activities) Exclusion Criteria: * cognitive impairment due to a developmental disability, psychiatric disorder, or substance abuse, or due to another type of brain injury, such as traumatic brain injury, stroke, or a progressive brain disease, such as Alzheimer's Dementia * current substance abuse disorder * diagnosis of postural orthostatic tachycardia syndrome (POTS) by a healthcare provider * prior cognitive processing speed training on DoubleDecision or a similar program * cannot tolerate taVNS * prior history of heart attack or other serious cardiac events * implanted medical device of any type * vasovagal syncope or history of fainting * history of seizures or epilepsy * temporomandibular Joint (TMJ) syndrome or other conditions that cause substantial jaw pain * history of peripheral nerve injury to the head, neck, or face * pregnant or breastfeeding * not able or willing to get an MRI scan * not able or willing to get a blood draw
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Alabama at Birmingham
RECRUITINGBirmingham, Alabama, 35294, United States
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