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Behavioural Intervention

Float Therapy for Sleep Quality

N/A
Waitlist Available
Research Sponsored by West Virginia University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Male or female 18-60 years of age
Be between 18 and 65 years old
Must not have
Has an injury requiring an orthopedic cast (i.e. plaster or synthetic), immovable splint or brace
Has skin ulcers, open rashes, incisions, stitches or large open wounds that could cause pain when exposed to saltwater
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 1, week 5, and week 9
Awards & highlights
No Placebo-Only Group

Summary

This trial compares traditional flotation therapy and Zerobody Dry Float technology to see how they affect sleep quality and stress levels in people with poor sleep and high stress. Flotation-REST is a treatment for deep relaxation, where a person is contained in a stimuli-restricted environment and floats in water with high salt content.

Who is the study for?
This trial is for men and women aged 18-60 who want to improve their sleep quality. It's not suitable for individuals taller than 76 inches, those with recent piercings or tattoos, a history of loss of consciousness or brain injury, skin conditions, certain medical devices, seizures in the last decade, weight over 250 pounds, motion sickness, communicable diseases or psychiatric conditions.
What is being tested?
The study compares two types of floatation therapy: Traditional Float-REST Therapy where participants float in saltwater tanks and Simulated Flotation Therapy that mimics this experience without water. The goal is to see which method better enhances sleep and overall well-being.
What are the potential side effects?
While flotation therapy is generally safe and relaxing, some may experience side effects such as discomfort from the high salt content if they have open wounds or skin sensitivity. Claustrophobia could be triggered due to the confined space of the tanks.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I am between 18 and 60 years old.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I am currently wearing a cast, splint, or brace that cannot be moved.
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I have open wounds or skin issues that saltwater could irritate.
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I have had a seizure within the last 10 years.
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I do not have any communicable diseases like HIV or Hepatitis.
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I have participated in a float-REST session within the last 3 months.
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I cannot control my bodily functions.
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I have been diagnosed with a psychiatric condition like schizophrenia or bipolar disorder.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 times a week, in 3 week increments, through study completion at 9 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 2 times a week, in 3 week increments, through study completion at 9 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in daily self-report measures for recovery
Change in daily self-report measures for task load
Change in daily self-report measures in perceived exertion
+11 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Simulated Flotation TherapyExperimental Treatment1 Intervention
Participants will utilize the Zerobody dry flotation therapy.
Group II: Traditional Float-REST TherapyActive Control1 Intervention
Participants will utilize sensory deprivation tanks.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for improving sleep quality include pharmacological options like melatonin, which helps regulate the sleep-wake cycle, and sedative-hypnotics that enhance GABA activity to induce sleep. Non-pharmacological treatments such as cognitive behavioral therapy for insomnia (CBT-I) address maladaptive thoughts and behaviors, while relaxation techniques like Tai Chi reduce stress and promote relaxation. These treatments are essential for sleep quality patients as they address the root causes of sleep disturbances, leading to better sleep and overall health.
The effect of acceptance and commitment therapy on insomnia and sleep quality: A systematic review.Non-Pharmacological Interventions to Improve Chronic Disease Risk Factors and Sleep in Shift Workers: A Systematic Review and Meta-Analysis.Tai Chi Improves Sleep Quality in Healthy Adults and Patients with Chronic Conditions: A Systematic Review and Meta-analysis.

Find a Location

Who is running the clinical trial?

West Virginia UniversityLead Sponsor
184 Previous Clinical Trials
64,373 Total Patients Enrolled

Media Library

Simulated Flotation Therapy (Behavioural Intervention) Clinical Trial Eligibility Overview. Trial Name: NCT04628910 — N/A
Sleep Quality Research Study Groups: Traditional Float-REST Therapy, Simulated Flotation Therapy
Sleep Quality Clinical Trial 2023: Simulated Flotation Therapy Highlights & Side Effects. Trial Name: NCT04628910 — N/A
Simulated Flotation Therapy (Behavioural Intervention) 2023 Treatment Timeline for Medical Study. Trial Name: NCT04628910 — N/A
~19 spots leftby Nov 2025