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Floating away trauma: could Sensory-Deprivation tanks ease PTSD in healthcare heroes?
NCT ID NCT07710417
First seen Jul 17, 2026 · Last updated Jul 17, 2026
Summary
This early-stage trial tests whether Floatation-REST — floating in a shallow, soundproof, light-free pool of Epsom salt water — can safely reduce post-traumatic stress symptoms and burnout in frontline healthcare workers and first responders. Fifteen participants will be randomly assigned to either float sessions or watch a documentary as a comparison. The study focuses on feasibility, safety, and whether the therapy lowers stress and burnout.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Floatation-REST (reduced environmental stimulation therapy via floatation in a shallow pool of Epsom salt water)
- What this could lead to
- If it works, this could offer a drug-free way to reduce post-traumatic stress and burnout in healthcare workers and first responders.
- What could go wrong
- This is a very early, small pilot study with only 15 participants, so results may not apply broadly. The therapy may cause discomfort or anxiety in some people.
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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Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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About 15 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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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.
- Ages
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18 to 64 years
- 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: 1. Work-related post-traumatic stress dysfunction as measured by either of the following inclusion pathways: (A) PTSS Pathway: PCL-5 greater than or equal to 20, OR meets criteria for full or partial PTSD on the MINI International Neuropsychiatric Interview 7 (DSM-V) (Criteria A + at least 2 B-E Criteria) OR (B) Functionally Anchored Pathway: evidence of work-related trauma exposure on the MINI International Neuropsychiatric Interview 7 (DSM-V) (Criterion A) or Life Events Checklist-5, and at least one of the following: Moral Injury and Distress Scale greater than or equal to 27, Sheehan Disability Scale greater than or equal to 5 on at least 1 of the 3 subscales, high or very high level of perceived stress (measured by PhenX Perceived Stress Scale greater than or equal to 16). 2. First responder or other emergency medical personnel 3. Ability to read, speak and understand English 4. Capable of providing consent Exclusion Criteria: 1. History of neurological conditions 2. Skin conditions or open wounds 3. DSM-5 diagnosis of psychotic spectrum disorders, obsessive-compulsive disorder, bipolar disorder, severe substance use disorder, or eating disorder 4. Inability to lay comfortably in a shallow pool of water 5. Failure to adhere to "pre-float checklist" 6. Breathalyzer test positive for alcohol or a drug-positive urine test 7. Unwillingness to provide consent or complete major aspects of protocol 8. MRI contraindications 9. Unstable medical diagnoses 10. Pregnancy 11. Evidence of inability to comply with study procedures based on experimenter judgement 12. Change in the dose or prescription of a medication within the 6 weeks before enrolling in the study that could affect brain functioning (e.g., anxiolytics, antipsychotics, antidepressants, benzodiazepines, or mood stabilizers)
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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 study's own enquiry address
This study publishes an address for enquiries. See it below .
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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
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Locations
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Laureate Institute for Brain Research
RECRUITINGTulsa, Oklahoma, 74136, United States
Contact Email: •••••@•••••
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