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Water Exercise and Memory Training for Long COVID Recovery

Tests a water-based exercise and memory training program in adults with long COVID symptoms.

Plain-language title generated from the registry record
Registry title: Water-based Activity to Enhance Recovery in Long COVID-19

Key facts

Where
Palo Alto, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 89 years old?

Source: NCT06142253, who can take part

Where in United States

  • VA Palo Alto Health Care System, Palo Alto, CAPalo Alto, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
VA Office of Research and Development
Trial code
NCT06142253
Record updated
18 June 2026
Original description
This two-year study will evaluate the feasibility and safety of an exercise + cognitive training program to improve neurological symptoms of long-COVID. This is a two-phased trial: 1) an exercise phase and 2) a cognitive training phase. The exercise phase will be an aquatic based exercise program. A combination exercise + memory training programs designed for persons with cognitive impairment have significantly improved memory more than other single intervention groups (exercise only, cognitive training only) and given the success of combination training programs with healthy adults, it is important to adapt these programs for persons with neurological symptoms of long-COVID.Read full original descriptionShow less

Water-based Activity to Enhance Recovery in Long COVID

This two-year study will evaluate the feasibility and safety of an exercise + cognitive training program to improve neurological symptoms of long-COVID. This is a two-phased trial: 1) an exercise phase and 2) a cognitive training phase. The exercise phase will be an aquatic based exercise program. A combination exercise + memory training programs designed for persons with cognitive impairment have significantly improved memory more than other single intervention groups (exercise only, cognitive training only) and given the success of combination training programs with healthy adults, it is important to adapt these programs for persons with neurological symptoms of long-COVID.

Inclusion: Veterans, age 18 to 89, of any racial or ethnic group; Previous COVID-19 infection at least 6 months after diagnosis documented in clinical record; Persistent neurological symptoms (e.g., "brain fog", cognitive impairment) occurring within 3 months of onset of COVID-19 infection and lasting at least 8 weeks in duration; Visual and auditory acuity to allow neuropsychological testing; Willingness to participate in clinical trial for 8 months; Approval by Primary Care Provider to participate in water-based physical exercise.

Exclusion: Psychiatric Exclusions; Current, uncontrolled severe psychotic disorder determined by the Mini International Neuropsychiatric Interview (MINI) Medical Exclusions; History of neurological (e.g., multiple sclerosis, seizure disorder, stroke,) neurodegenerative (e.g., Parkinson's disease, Alzheimer's disease) or system illness affecting CNS function (e.g., liver failure, kidney failure, congestive heart failure, systemic cancer) occurring before COVID-19 diagnosis; Current severe cardiac disease (e.g., uncontrolled atrial fibrillation, defined as mean 24 hour heart rate >85 beats/min, or 24 hour maximal ventricular rate >150 beats/min; uncontrolled ventricular arrhythmias, defined as recurrent ventricular tachycardia >3 beats in succession, or 24 hour PVC count >20%; active pericarditis or myocarditis; Class III/IV heart failure and / or ejection fraction < 20%; thrombophlebitis; pulmonary disease with a drop in O2 Sat with exercise to 90% without oxygen; embolism within past 6 months); Inability to participate in an exercise stress test; Inability to read, verbalize understanding and voluntarily sign the Informed Consent.

ClinicalTrials.gov NCT06142253