Tune Up Your Back: Soundwave Wellness Study

NCT07256626 | Enrolling By Invitation

• 1 other identifier: 37378
• Study Type: interventional
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

Looking to support your back mobility and overall comfort? Join our study exploring WAVwatch 2.0, an innovative soundwave therapy device. This non-invasive technology is designed for individuals who want to maintain easy movement and flexibility without constantly reaching for over-the-counter options. By joining, you'll discover how this gentle approach may help support everyday back comfort, mobility, and flexibility.

Conditions

Pain, Back

Outcome Measures

Primary Outcomes (3)

• PROMIS® Item Bank/Scale v.2.0 - Pain Behavior Survey

  This survey aims to understand individual behaviors and reactions when experiencing pain within the past 7 days.

  Change from baseline (Day 1-3) in pain behavior at 4 weeks after the start of the intervention (Day 27-33)

• Quality of Life and Health Survey

  This survey asks about your feelings towards your quality of life, health, and various areas of your life. It covers your experiences and feelings in the past four weeks. Please choose the answer that appears most appropriate.

  Change from baseline (Day 1-3) in quality of life at 4 weeks after the start of the intervention (Day 27-33)

• ROMIS® Numeric Rating Scale v.1.0 - Pain Intensity 1a

  This survey is designed to understand the level of pain experienced by the participant in the past 7 days. The responses will help in assessing the pain intensity from no pain to worst imaginable pain.

  Change from baseline (Day 1-3) in pain intensity at 1 week after the start of the intervention (Day 4-10)

Study Arms (1)

Single arm where participants act as their own control

EXPERIMENTAL

Single arm where participants act as their own control

Device: WAVWatch 2.0

Interventions

WAVWatch 2.0 DEVICE

The WAVwatch sound frequency therapy device employs acoustic waves absorbed through the skin to promote wellness, with manufacturers and users reporting minimal safety risks

Single arm where participants act as their own control

Eligibility Criteria

• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

• Can read and understand English.
• US resident.
• Willing and able to follow the requirements of the protocol.

Sponsors & Collaborators

• Efforia, Inc: lead

Study Sites (1)

Efforia

New York, New York, 10003, United States

Location

Related Links

• Additional information and join instructions on Efforia

MeSH Terms

Conditions

Back Pain

Condition Hierarchy (Ancestors)

Pain; Neurologic Manifestations; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Single Arm observational where participants act as their own control

Study Record Dates

• First Submitted: November 20, 2025
• First Posted: December 1, 2025
• Study Start: August 25, 2025
• Primary Completion (Estimated): August 25, 2026
• Study Completion (Estimated): August 25, 2026
• Last Updated: December 26, 2025

Record last verified: 2025-11

Locations

US (1)