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Completed

NCT Number: NCT05451888

Assessing Effects of Mineral-rich Floatation Spa Treatment on Mood and Psychological Health Outcomes

This is a randomised parallel groups trial in healthy human adults exploring whether 8 weeks of treatment in various different spa pools is associated with benefits for mood and other psychological outcomes. Outcome measures will be taken at the beginning and the end of the 8 week period. In addition, outcome measures will be taken after the first spa session to assess acute effects.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

School of Psychology

Reading, Berkshire, RG66AL, United Kingdom

About this study

This experiment is investigating whether mineral-rich floatation spa treatments influence mood and psychological health outcomes. The study will be undertaken at Nirvana Spa in Wokingham over a duration of 8 weeks for each participant. Participants will be randomly allocated to one of three experimental groups. Each group will be assigned to a different mineral-rich spa treatment pool; either a Celestial Floatation pool, Dead Sea Salt Therapy pool, or a control pool which does not contain any minerals (Balneotherapy pool). Participants will undergo one 40-minute treatment, once a week for 8 weeks. The recommended duration for Dead Sea Salt and Celestial floatation pool sessions are 30-40 minutes, thus this study will reflect everyday consumer behaviour. A follow-up assessment of the outcome measures will take place 2 weeks after cessation of treatment to assess possible carry-over effects.

Specifically, there are four research aims of the study;

  • To investigate the effects of regular weekly treatment in the Celestial Floatation Pool on mood outcomes including positive and negative affect, anxiety, depression, and stress.
  • To investigate the effects of regular weekly treatment in the Dead Sea Salt Therapy pool on mood outcomes including positive and negative affect, anxiety, depression, and stress.
  • To investigate the effects of a single 40-minute treatment in the Celestial Floatation Pool and the Dead Sea Salt Therapy pool on mood outcomes including positive and negative affect, anxiety and stress.
  • Do any beneficial effects of spa treatment persist beyond cessation of treatment?

Outcome measures will be used to assess mood and psychological health outcomes both at the beginning (baseline) and at the end (8 weeks) of each treatment (see procedures). In addition, outcome measures will be taken immediately after the first spa treatment to assess acute effects. Specifically, the outcome measures are:

  • Positive and Negative Affect using the PANAS-X. This will be a well-established measure of how positive and negative an individual is feeling (these are two separate outcome measures).
  • Subjective mood with the Immediate Mood Scaler. This is a recently published novel 22-item measure developed to assess dynamic components of mood. Participants rate their current mood state on a continuum using 7-point Likert scales (eg, happy-sad, distracted-focused, sleepy-alert, fearful-fearless. For each item, an integer score between 1 and 7 is derived. The total score for this scale is the sum of the scores on all 22 items.
  • Stress using the Perceived Stress Scale.
  • Anxiety with the GAD-7 and the Spielberger State Anxiety Inventory.
  • Depression with the PHQ-8
  • Sleep quality with the Pittsburgh Sleep Quality Index (PSQI)
  • Experience of spa use will be captured using qualitative and quantitative questions on their enjoyment of the spa intervention and ease of use.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Any adult

Exclusion criteria

Any diagnosed mental health conditions or physical conditions/injuries (including those still undergoing physiotherapy for a previous condition or injury), arthritis and previous regular use of spa treatments which is defined as use of spa facilities once a month or more over the previous 8 weeks. The rational for these exclusion criteria is that the spa is known to benefit injury and joint pain recovery. This is not a mechanism of interest for this study, therefore we want to exclude these participants.

Treatment and study plan

Spa treatment

Behavioral

A 40 minute period of lying in the spa treatment pool

Primary outcomes

  1. Positive Affect (chronic)

    Time frame: Change between baseline and 8 weeks

    This will be a well-established measure of how positive an individual is feeling measured using the PANAS-X questionnaire

  2. Negative Affect (chronic)

    Time frame: Change between Baseline and 8 weeks

    This will be a well-established measure of how negative an individual is feeling measured using the PANAS-X questionnaire

Secondary outcomes

  1. Subjective mood

    Time frame: Change between baseline and 8 weeks

    Assessed with the Immediate Mood Scaler

  2. Subjective Stress

    Time frame: Change between baseline and 8 weeks

    Assessed with the Perceived Stress Scale

  3. Anxiety

    Time frame: Change between baseline and 8 weeks

    Assessed with the GAD-7 and the Spielberger State Anxiety Inventory

  4. Depression

    Time frame: Change between baseline and 8 weeks

    PHQ-8

  5. Sleep Quality

    Time frame: Change between Baseline and 8 weeks

    Pittsburgh Sleep Quality Index (PSQI)

  6. Subjective experience of the spa

    Time frame: At 8 weeks

    captured using qualitative and quantitative questions on their enjoyment of the spa intervention and ease of use.

Sponsors and collaborators

Lead sponsor

University of Reading

Other

Registry information

Acronym: USS

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Jul 11, 2022
Registry last updated
May 26, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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