Floatation Experience in Nurses and Physicians

Sponsor
Mercy Health Ohio (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05977894
Collaborator
(none)
50
1
11.5
4.3

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Reduced Environmental Stimulation Therapy

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.

Study Design

Study Type:
Observational
Anticipated Enrollment :
50 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Wellbeing Monitoring During Sequential Reduced Environmental Stimulation-Floatation
Anticipated Study Start Date :
Aug 15, 2023
Anticipated Primary Completion Date :
Jul 31, 2024
Anticipated Study Completion Date :
Jul 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Nurses and physicians

Nurses (registered, practitioner, and anesthetist) and physicians, employed at St. Elizabeth Youngstown Trauma Center, Mercy Health

Other: Reduced 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.
Other Names:
  • Floatation-REST
  • Outcome Measures

    Primary Outcome Measures

    1. Change in the inventory wellbeing score [Through study completion, an average of 1 year]

      The sum of the positive affect and nonstress scores (range 11-55)

    Secondary Outcome Measures

    1. Change in the nonstress score [Through study completion, an average of 1 year]

      The sum of the reverse-scored ratings for the 7 negative affect items (range 7-35)

    2. Change in the positive affect score [Through study completion, an average of 1 year]

      The sum of the ratings for the 4 positive affect items (range 4-20)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    21 Years to 70 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Nurses and physicians
    Exclusion Criteria:
    • Any person that is not a physician or nurse at St. Elizabeth Youngstown Hospital

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 St. Elizabeth Youngstown Hospital Youngstown Ohio United States 44501

    Sponsors and Collaborators

    • Mercy Health Ohio

    Investigators

    • Principal Investigator: C. Michael Dunham, MD, Mercy Health Ohio

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    C. Michael Dunham, Research Investigator, Mercy Health Ohio
    ClinicalTrials.gov Identifier:
    NCT05977894
    Other Study ID Numbers:
    • 6120-810-1-01
    First Posted:
    Aug 7, 2023
    Last Update Posted:
    Aug 7, 2023
    Last Verified:
    Aug 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by C. Michael Dunham, Research Investigator, Mercy Health Ohio
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 7, 2023