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NCT Number: NCT06619418

Assessment of Usability and Satisfaction With a Take-home Device Presenting Sound and Body Stimulation for Back Pain

Pain symptoms can have a variety of ways to be treated, from medications to physical therapy, with several options being available to patients. However, no one treatment may work for all people who experience pain, especially cLBP. The purpose of this study is to measure the compliance, usability, and satisfaction of an at-home, multi-modal stimulation device in a diverse population of people with chronic lower back pain (cLBP). The multi-modal device will include a combination of electrical stimulation, auditory stimulation, and integrative-health techniques, including mindfulness breathing, health coaching, and reflective journaling. The multi-modal device creation is based on prior knowledge in lower back pain treatment, which includes electrical stimulation of the back (Transcutaneous Electrical Nerve Stimulator or TENS) and integrative health modalities. In isolation, these treatments are only somewhat effective in reducing symptoms.

This pilot study will involve participants who experience cLBP as we investigate a novel at-home, multi-modal device design. The main objective of the pilot usability study is to examine compliance to the intended use of the multi-modal device and approach, as well as protocol feasibility, and satisfaction with the settings and design.

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Key information

Conditions

Chronic Lower Back Pain

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Minnesota

Minneapolis, Minnesota, 55414, United States

Location status: Recruiting

Location contact

Grace Conchas

CONTACT

[email protected]

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Must be 18 years of age or older
  • Must be within commuting distance to the University of Minnesota
  • Able to provide consent and follow study instructions
  • Must be able to understand English
  • Must have chronic LBP, which is defined as lower back pain for more than 3 months
  • A score of 4 or higher on the PEG
  • Must be willing to commit to full duration of the study
  • Not currently taking any benzodiazepines or sedative hypnotics

Exclusion criteria

  • Back Pain associated with:
  • Spondylolisthesis or spinal stenosis
  • Sciatica or radiculopathy
  • Rhematologic or inflammatory disease
  • Trauma, fracture, dislocation, or previous back surgery
  • A score of 10 on the PEG
  • Pregnant
  • Have an electrically implanted device, such as a pacemaker.
  • Heart Disease
  • Epilepsy
  • Cancer
  • Psychiatric conditions including psychosis, suicidal ideation, or substance abuse disorder
  • A pure tone average of more than 40 dB HL at 500 dB, 1000 dB, or 2000 dB HL.
  • Individuals currently using other lower back pain treatments during the study in which they are unable to maintain a steady state while participating in our study for one month before beginning the multi-modal regimen.

Treatment and study plan

TENS device

Device

will be using an FDA- cleared TENS device for electrical stimulation (TENS 7000, Compass Health Brands) in combination with commercially-available headphones for acoustic stimulation (AKG 845 BT).Will be shown how to use the device, trained on the multimodal stimulation procedure, and sent home with the device for 12 weeks.

Integrative health modalities

Behavioral

will be instructed on the integrative health modalities for this study. They will be given a tablet that includes the videos for the visually guided deep breathing. They will also receive the reflective journal and be set up for health coaching visits. At the end of the 12 weeks, this group of participants will return to the U of M campus and complete an interview about satisfaction and usability of the IH modalities.

Primary outcomes

  1. compliance rate

    Time frame: 12 weeks

    Measure compliance in terms of time using the integrative health devices and the multi-modal stimulation device over a period of 12 weeks to determine the effect on participant compliance by adding electrical stimulation to the device.

Secondary outcomes

  1. satisfaction rate

    Time frame: 12 weeks

    relating to usability of an at-home multi-modal stimulation approach and device and integrative health practices..

Study contacts

Contact information is provided by the study sponsor or research team.

Grace Conchas

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

University of Minnesota

Other

Registry information

Important dates

Study start
2024
Primary completion
2026
Study completion
2026
First posted
Oct 1, 2024
Registry last updated
Aug 13, 2025

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

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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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