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Floatation Experience in Nurses and Physicians

Wellbeing Monitoring During Sequential Reduced Environmental Stimulation-Floatation

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05977894
Enrollment
50
Registered
2023-08-07
Start date
2023-10-28
Completion date
2026-05-05
Last updated
2025-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burnout, Burnout, Professional, Negative Affect, Positive Affect, Psychological, Wellbeing

Keywords

Floatation, Anxiety, Attention, Awareness, Burnout, Relaxation Therapy, Self-concept, Wellbeing

Brief summary

The goal of this observational study is to monitor the floatation experience and continue the program as long as deemed important. The main question it aims to answer is: will inventory wellbeing scores increase according to the number of floatation sessions accrued? Nurses (registered, practitioner, and anesthetist) and physicians, employed at St. Elizabeth Youngstown Trauma Center, Mercy Health, will be welcomed to participate in the floatation experience. Participants will be given an option to complete the Wellbeing Inventory survey prior to each floatation session.

Detailed description

The floatation program is a Mercy Health enterprise sponsored by the Mercy Health Mahoning Valley Foundation.The goal of this study is to monitor the floatation experience and continue the program as long as deemed important. The investigators hypothesize that inventory wellbeing scores will increase according to the number of floatation sessions accrued. Nurses (registered, practitioner, and anesthetist) and physicians, employed at St. Elizabeth Youngstown Trauma Center, Mercy Health, will be welcomed to participate in the optional floatation program in Warren, Ohio at no financial cost to them. They will become aware of floatation options through the Mercy Health Be Well wellness program. Floatation monitoring will include assessments of wellbeing, nonstress, and positive affect scores. Participants will be given an option to complete the Wellbeing Inventory survey prior to each floatation session. This will be a self-reporting anonymous process. The investigator will never know the identity of the participant.

Interventions

OTHERReduced Environmental Stimulation Therapy

During floatation-REST (Reduced Environmental Stimulation Therapy), the participant enters a tank that is approximately 5 feet wide, 7 feet long and 5 feet high. The tank is filled with a 10 inch height of water containing enough Epsom salt (magnesium sulfate) to create body buoyancy. The water temperature is 93.5 degrees F, an approximate equivalent for normal skin temperature. Ear plugs are used to mitigate sound and the tank is without light illumination to prevent visual stimulation. The sessions are typically 60 minutes in duration. The individual is Floating-in Solitude, Darkness, Silence, and Thermal-Neutrality. This experience reduces external sensory nervous system input and creates an extraordinarily deep state of mental and physical relaxation.

Sponsors

Mercy Health Ohio
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Nurses and physicians

Exclusion criteria

* Any person that is not a physician or nurse at St. Elizabeth Youngstown Hospital

Design outcomes

Primary

MeasureTime frameDescription
Change in the inventory wellbeing scoreThrough study completion, an average of 1 yearThe sum of the positive affect and nonstress scores (range 11-55)

Secondary

MeasureTime frameDescription
Change in the nonstress scoreThrough study completion, an average of 1 yearThe sum of the reverse-scored ratings for the 7 negative affect items (range 7-35)
Change in the positive affect scoreThrough study completion, an average of 1 yearThe sum of the ratings for the 4 positive affect items (range 4-20)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026