Can a scented massage boost brain function in ICU patients?
NCT ID NCT07593430
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will test whether a daily aromatherapy massage, combined with a sensory stimulation program, can improve cognitive function in intensive care patients with brain injuries. Sixty adults on ventilators or oxygen will be randomly assigned to receive the treatment from a family member, a nurse, or standard care. The goal is to see if this gentle approach can help patients become more aware and responsive.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- aromatherapy massage with orange, patchouli, and rosemary oils
- What this could lead to
- If it works, this could offer a simple, drug-free way to help ICU patients regain awareness and shorten their hospital stay.
- What could go wrong
- This is a small, early-stage study with only 60 people. It is not yet recruiting, so results are unknown. The effect may be small or no different from standard care.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
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 to 90 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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 diagnosed with acute brain injury, * Glasgow Coma Score (GCS) between 6 and 12, * Intubated or monitored on oxygen, * 18 years of age or older, * Between 24 and 48 hours after hemodynamic vital signs stabilized and without a history of delirium, * Patients without a history of diseases that increase the risk of odor sensitivity, such as epilepsy or asthma, Exclusion Criteria: * Glasgow Coma Score (GCS) below 6, * Hemodynamic instability, * Continuously using neuromuscular blocking agents during the study, * Changes in treatment schedule during the study, * History of diseases that increase the risk of odor sensitivity, such as epilepsy or asthma,
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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 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.
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