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NCT07221318 · ClinicalTrials.gov registry record · NA
Evaluating a Mat-Based Biometric Vibration System for Sleep and Daily Recovery
A NA study of Healthy Adult Male and Female Volunteers, sponsored by Florida International University.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT07221318: Recruiting NA study of Healthy Adult Male and Female Volunteers, sponsored by Florida International University.
NCT07221318 is a NA study of Healthy Adult Male and Female Volunteers that is actively recruiting participants, run by Florida International University. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07221318, a NA study of Healthy Adult Male and Female Volunteers, is actively recruiting participants, sponsored by Florida International University.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this randomized clinical trial is to learn whether a low-frequency "kinetic wellness" mat (a comfortable mat that gently vibrates) can improve stress recovery, sleep quality, mood, and attention in healthy adults ages 18-45. The main questions it aims to answer are: * After 3 weeks, does regular use of the vibrating mat increase heart rate variability (a noninvasive marker of the body's ability to recover from stress) and improve sleep, mood, perceived stress, and anxiety compared with no mat use? * Do patterns of resting brain activity (measured with EEG) and heart rate variability (HRV) change from before to after the program, and are those changes related to each other? Researchers will compare two groups: an Experimental group that uses the vibrating mat at home for 3 weeks, and a Control group that does not use the mat. Participants are randomly assigned to a group. Participants will: * Attend two lab visits (\~60 min) for questionnaires, resting heart activity (HRV) and brain activity (EEG), and a brief attention test. * On 3-4 days per week for 3 weeks: * Experimental group: use the vibrating mat for 15 minutes while recording HRV. * Control group: lie quietly for 15 minutes while recording HRV. * Both groups: record HRV for 15 minutes before bedtime and 15 minutes after waking on those same days. * Both groups: complete quick check-ins on feelings (after sessions and the next morning) and log caffeine/alcohol, exercise, and medications.
Primary Outcome
Eyes-closed 15-minute, supine resting EEG using a 24-channel Smarting Mobi system. Preprocessing: 0.5-30 Hz band-pass, ocular SSP, ±100 µV artifact rejection, common-average reference; clean data segmented into 10-s epochs. Outcome is band power in Theta (4-8 Hz), Alpha (8-13 Hz), Beta (13-30 Hz), averaged across all electrodes and epochs (units: power; may be log-transformed for analysis). Higher values indicate stronger oscillatory activity in each band. Primary analysis compares Post-Baseline
Conditions Studied
Interventions
- DEVICE Low-frequency whole-body vibration mat
Study Locations (1)
Florida
- Florida International University, Biscaney Bay Campus - Miami
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2025-10-06 |
| Est. Completion | 2026-05 |
| Phase | NA |
What NCT07221318 shows while recruiting
NCT07221318 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 1 condition, with Healthy Adult Male and Female Volunteers appearing as the primary indexed condition, and to 1 intervention - of which Low-frequency whole-body vibration mat is the first listed.
NCT07221318 reports a single indexed study location in Florida.
Frequently Asked Questions
What is clinical trial NCT07221318 about?
NCT07221318 is a clinical study titled "Evaluating a Mat-Based Biometric Vibration System for Sleep and Daily Recovery". The goal of this randomized clinical trial is to learn whether a low-frequency "kinetic wellness" mat (a comfortable mat that gently vibrates) can improve stress recovery, sleep quality, mood, and attention in healthy adults ages 18-45. The main questions it aims to answer are: * After 3 weeks, do...
What is the current status of trial NCT07221318?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2025-10-06. Estimated completion is 2026-05.
What conditions does trial NCT07221318 study?
This clinical trial studies the following conditions: Healthy Adult Male and Female Volunteers.
What interventions are being tested in trial NCT07221318?
The interventions under investigation include: Low-frequency whole-body vibration mat (DEVICE).
Who is sponsoring clinical trial NCT07221318?
This trial is sponsored by Florida International University, which has 89 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07221318 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT07221318's enrollment target sits among peer trials
50 1279th of 2000 higher than 622 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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