Healthcare Practioner
QUICK REFERENCE GUIDE
Evidence-Based Resource for Clinical Decision-Making
WHAT IS FLOTATION-REST?
Flotation-REST is a non-pharmacological intervention involving sensory reduction in a specialized tank containing skin-temperature (35°C) water saturated with magnesium sulfate (Epsom salt). High buoyancy allows effortless floating, while reduced sensory input (darkness, sound attenuation) facilitates deep relaxation and parasympathetic nervous system activation.
Mechanism of Action:
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Parasympathetic nervous system activation
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Reduced sensory input allowing nervous system reset
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Decreased functional connectivity between pain and emotional processing networks
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Possible transdermal magnesium absorption
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Enhanced interoceptive awareness
EVIDENCE-BASED CLINICAL APPLICATIONS
Primary Indications Supported by RCT Evidence
1. GENERALIZED ANXIETY DISORDER (GAD)
Evidence Level: RCT with waitlist control
Key Study: Jonsson & Kjellgren (2016) - BMC Complementary and Alternative Medicine
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Design: RCT (n=50), 12 sessions over 7 weeks
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Primary Outcome: GAD-symptomatology significantly reduced in treatment group (p<.001) vs. waitlist control (p>.05)
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Remission Rate: 37% achieved full remission in treatment group vs. 14% in control
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Effect Size: ηp² = .062 for GAD symptoms
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Secondary Benefits:
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Sleep quality: 43% achieved "good sleeper" status (ηp² = .16)
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Depression: 42% full remission (ηp² = .34)
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Emotion regulation difficulties: Significant improvement (ηp² = .16)
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Durability: Effects maintained at 6-month follow-up (except depression)
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Safety: No adverse events reported
Clinical Note: While GAD core symptom (pathological worry) showed limited response, physiological manifestations (restlessness, muscle tension, fatigue) demonstrated robust improvement.
2. ANXIETY SENSITIVITY & ACUTE ANXIETY
Evidence Level: Multiple RCTs
Key Study: Feinstein et al. (2018) - Biological Psychiatry: Cognitive Neuroscience and Neuroimaging
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Design: RCT comparing 90-minute float vs. relaxing film condition
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Results: Float condition produced significantly greater reductions in:
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State anxiety (STAI): Large effect size
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Muscle tension: Significant reduction
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Blood pressure: Both SBP and DBP decreased
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Enhanced cardiorespiratory interoceptive awareness
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Safety: No serious adverse events across 50 participants
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Clinical Significance: More severe baseline anxiety associated with greater benefit
Additional Evidence:
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Garland et al. (2024): 6-session protocol showed 85-89% adherence, no serious adverse events
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Positive experiences endorsed more commonly than negative, with higher intensity ratings
3. CHRONIC PAIN
Evidence Level: Mixed findings from RCTs
Key Study: Loose et al. (2021) - JAMA Network Open
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Design: RCT (n=99) with placebo and waitlist controls, 5 sessions
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Long-term Results: No significant between-group differences at 1, 12, or 24 weeks
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Short-term Results: Significant within-group improvements immediately post-session:
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Pain intensity: -17.0 points (p<.001)
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Anxiety: -10.1 points (p<.001)
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Relaxation: +23.9 points (p<.001)
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Pain area: -3.6% (p<.001)
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Earlier Studies (Pre-2021):
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Kjellgren et al. (2001, 2009): Multiple studies showing benefits for stress-related muscle pain
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Bood et al. (2005-2007): 12-33 sessions demonstrated sustained improvements in pain, anxiety, depression, sleep quality
Clinical Interpretation: Evidence suggests:
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Acute session benefits are robust
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Long-term benefits may require >5 sessions (earlier studies used 12-33 sessions)
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Best suited for stress-related and musculoskeletal pain conditions
Float PROTOCOLS
CHRONIC PAIN
Intensive Phase:
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Frequency: 2-4 sessions per week
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Duration: 90-minute sessions recommended
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Course Length: Up to 1 month (8-16 sessions)
Maintenance Phase:
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Frequency: 1-2 sessions per month
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Duration: 90 minutes
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Indication: Continue as long as therapeutic benefit maintained
ANXIETY DISORDERS
Initial Phase:
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Session 1: 60 minutes (assess tolerance)
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Subsequent Sessions: 60-90 minutes based on patient preference
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Frequency: 1-2 sessions per week
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Course Length: Until noticeable anxiety reduction (typically 6-12 sessions)
Maintenance Phase:
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Frequency: 1-2 sessions per month
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Adjustment: Add extra sessions during high-stress periods
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Duration: 60-90 minutes
SAFETY PROFILE
Systematic Review Evidence
Multiple RCTs report no serious adverse events associated with flotation-REST.
Common Minor Side Effects (typically mild):
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Transient skin itchiness
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Dry mouth
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Saltwater contact with eyes (preventable with proper instruction)
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Discomfort if saltwater contacts open wounds or cuts
Positive Effects (More Common Than Negative): Studies consistently show positive experiences endorsed more frequently and at higher intensity than negative experiences. Most participants (>95%) express desire to repeat treatment.
CONTRAINDICATIONS
Absolute Contraindications
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Active psychosis or history of severe psychotic episodes
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Uncontrolled epilepsy
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Open wounds or active skin infections
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Severe claustrophobia (unless modified protocol with open tank/light options)
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Acute intoxication (alcohol or substances)
Relative Contraindications (Requires Physician Evaluation)
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Recent surgery (within 2-4 weeks, depending on site)
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Severe uncontrolled cardiovascular disease
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Pregnancy (particularly first trimester - consult OB/GYN)
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Pacemaker or implanted cardiac device (evaluate case-by-case)
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History of dissociative disorders (requires close monitoring)
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Recent significant trauma or PTSD (may require modified introduction)
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Active suicidal ideation (requires stabilization first)
Special Populations
Pregnancy: Limited evidence; consult obstetrics. Theoretical benefits for stress/pain management but requires individualized risk assessment.
Elderly: Generally safe; consider assistance entering/exiting tank and cardiovascular clearance.
Pediatric: Minimal evidence; not routinely recommended for patients <18 years.
CLINICAL DECISION ALGORITHM
Step 1: Screen for Indications
Consider Float Therapy for:
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GAD with prominent somatic symptoms
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Chronic stress-related muscle pain
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High anxiety sensitivity
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Patients seeking non-pharmacological options
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Adjunct to CBT or other psychotherapy
Step 2: Assess Safety
Review contraindications (see above)
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Absolute contraindications → Do not refer
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Relative contraindications → Evaluate risk/benefit, consider consultation
Step 3: Set Expectations
Educate patient on:
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Treatment involves floating in sensory-reduced environment
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Typical session: 60-90 minutes
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Course of treatment: 6-12 sessions for anxiety, 8-16 for pain
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Evidence shows short-term benefits; long-term effects require maintenance
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Not a substitute for evidence-based first-line treatments
Step 4: Provide Referral
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Direct Referral to Kairos Float & Wellness Studio
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Greenville, NC 27858
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Contact: Rebecca.Harris@kairosfloats.com
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Evidence-based protocols
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Clinical-grade sanitation (AOP system, FDA Class 1 drinking water standards)
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Two Deluxe Float Suites (6.5' wide, 8' long, 7.5' ceilings)
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General Float Center Guidance
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Verify sanitation standards (UV, ozone, filtration systems)
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Confirm staff training in clinical applications
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Ensure accessibility features (intercom, lighting control, emergency protocols)
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Ask about protocols for anxious/clinical populations
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BILLING & INSURANCE CONSIDERATIONS
Current Status (2024-2025):
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Float therapy is not currently covered by most insurance plans
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No established CPT codes for flotation-REST
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Patients pay out-of-pocket (typically $50-100 per session)
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Some HSA/FSA accounts may reimburse with physician letter of medical necessity
Documentation for Medical Necessity, Include in referral:
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Primary diagnosis (ICD-10 code)
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Failed or suboptimal response to conventional treatments
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Contraindications to pharmacological options (if applicable)
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Clinical rationale for non-pharmacological intervention
WHEN TO CONSIDER FLOAT THERAPY
Strong Consideration
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GAD with inadequate response to first-line CBT
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Patient preference for non-pharmacological intervention
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Chronic pain with prominent anxiety/stress component
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Multiple failed medication trials
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Contraindications to standard treatments
Adjunctive Consideration
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Alongside CBT for anxiety disorders
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Stress management for chronic medical conditions
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Athletic recovery and performance enhancement
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Burnout prevention in high-stress occupations
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Sleep disturbance secondary to anxiety
Low Priority
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Acute psychiatric crisis (stabilize first)
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When evidence-based first-line treatments haven't been tried
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Severe depression without anxiety component
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Primary pathological worry without somatic symptoms
MONITORING & FOLLOW-UP
Recommended Assessment Schedule
Baseline:
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GAD-7 (anxiety) or VAS (pain)
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Document current medications
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Establish treatment goals
Week 4 (Mid-treatment):
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Brief symptom check
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Assess tolerance and adherence
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Address any concerns
Week 8-10 (Post-treatment):
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Repeat baseline measures
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Assess clinical significance of change
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Determine need for maintenance protocol
3-6 Months:
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Long-term follow-up
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Reassess need for additional sessions
KEY TAKEAWAYS
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Flotation-REST has Level 1 evidence (RCT) for anxiety reduction, particularly GAD with somatic symptoms
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Safety profile is excellent - no serious adverse events reported across multiple RCTs
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Typical protocol: 6-12 sessions (60-90 min), 1-2x/week, then maintenance
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Best candidates: GAD, high anxiety sensitivity, stress-related pain, patients seeking non-drug options
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Absolute contraindications: Active psychosis, uncontrolled epilepsy, open wounds, severe claustrophobia
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Not covered by insurance - patient pays out-of-pocket ($50-100/session), some float centers accept HSA/FSA (Kairos is HSA/FSA Eligible)
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Evidence strongest for short-term benefits - long-term effects require maintenance sessions


