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ICU Survivors' brain health under the microscope
NCT ID NCT00392795
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study follows 826 ICU survivors to understand why some develop long-term thinking and memory problems. Researchers will look at factors like delirium and sedative use during the ICU stay. The goal is to find modifiable risks that could lead to better prevention and recovery strategies.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could identify which factors in the ICU cause long-term brain problems, pointing toward ways to prevent or treat them.
- What could go wrong
- This is an observational study, not a treatment trial. It may only find associations, not causes, and results might not apply to all ICU patients.
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.
- Participants
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826 people
The number who actually took part.
- Start date
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Jan 2007
- Expected to finish
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Dec 2026
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.
Who is studied
Medical and Surgical ICUs
- 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: * Patients will be included if they are adult, patients in a medical and/or surgical ICU receiving treatment for any of the following: respiratory failure or cardiogenic or septic shock. Exclusion Criteria: Patients who meet the inclusion criteria will be excluded if they meet any of the following criteria: * Cumulative ICU time \>5 days in the past 30 days, not including the current ICU stay, as this might create a state of flux regarding patients' cognitive baseline * Severe cognitive or neurodegenerative diseases that prevent a patient from living independently at baseline, including mental illness requiring institutionalization, acquired or congenital mental retardation, known brain lesions, traumatic brain injury, cerebrovascular accidents with resultant moderate to severe cognitive deficits or ADL dependency, Parkinson's disease, Huntington's disease, severe Alzheimer's disease or dementia of any etiology * ICU admission post cardiopulmonary resuscitation with suspected anoxic injury * An active substance abuse or psychotic disorder, or a recent (within the past 6 months) serious suicidal gesture necessitating hospitalization. This exclusion will enrich follow-up rates by avoiding patients with whom it is particularly challenging to maintain long-term contact * Blind, deaf, or unable to speak English, as these conditions would preclude our ability to perform the follow-up evaluation interviews. * Overly moribund and not expected to survive for an additional 24 hours and / or withdrawing life support to focus on comfort measures only. * Prisoners. * Patients who live further than 200 miles from Nashville and who do not regularly visit the Nashville area. * Patients who are homeless and have no secondary contact person available. This exclusion will enrich follow-up rates by avoiding patients with whom it is particularly challenging to maintain long-term contact * The onset of the current episode of respiratory failure, cardiogenic shock, or septic shock was \> 72 hours ago. * Patients who have had cardiac bypass surgery within the past 3 months (including the current hospitalization)
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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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Saint Thomas Hospital
Nashville, Tennessee, 37205, United States
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Vanderbilt University Medical Center
Nashville, Tennessee, 37232, United States
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