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ENROLLING BY INVITATION

NCT07011537

Examining the Impact of a Digital Health Program and TENS Device for Patients With Chronic Low Back Pain

Sponsor: Hinge Health, Inc

View on ClinicalTrials.gov

Summary

The goal of this study is to examine the extent to which Hinge Health, a digital musculoskeletal program, and Enso, a wearable pain relief device, have clinically significant impact on the pain, function, and health care use among patients undergoing non-imperative care for chronic lower back pain.

Official title: The Hinge Health and ENSO Back Pain Study: Prospective, Open-label, Randomized Superiority Trial of a Digital Health Program and High Frequency Impulse Therapy (HFIT) Versus Standard of Care in Treatment of Chronic Low Back Pain

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

196

Start Date

2026-01-16

Completion Date

2026-07

Last Updated

2026-01-23

Healthy Volunteers

Conditions

Back Pain Lower Back Chronic Chronic Pain Musculoskeletal Pain

Interventions

BEHAVIORAL

Digital Musculoskeletal (MSK) Program

Hinge Health is a digital MSK program to help participants manage chronic MSK pain through offering exercise therapy sessions, educational articles, and personal health coaching. Hinge Health delivers exercise therapy sessions and education through "playlists" accessed through the program app. Each playlist consists of three to seven exercises specific to the body region(s) the participant experiences pain in. Animations and videos, while paired with sensors and computer vision, demonstrate how to perform exercises, the number of repetitions for each exercise, and how long to hold positions. Playlists present more challenging exercises and/or more repetitions as participants progress further along in the program. After participants complete the exercises, the playlist delivers educational articles and resources focused on MSK pain-related topics, including lifestyle changes, pain neuroscience, and social support.

DEVICE

Transcutaneous Electrical Nerve Stimulation (TENS)

The Enso is a strong complement/enhancement to the Hinge Health program, as it helps users to better manage their pain in order to work through their exercise sessions in the program. The Enso device is not intended to be a stand-alone solution; it provides pain relief, but exercise therapy provides important long-term benefits. Participants will use the digital MSK program (Hinge Health) in combination with a pain management device (Enso).

OTHER

Standard of Care (SOC)

The control group will continue to receive the access to traditional medical care for their MSK needs through their healthcare provider. Upon study completion, control group members who complete all follow-up surveys will receive Hinge Health membership and an Enso device for free for 12 months, starting at the conclusion of their participation in the study.

Inclusion Criteria: * Age 18 or over * United Healthcare (UHC) is primary health plan * Mechanical (myofascial), axial back pain (focused around the spine) * Experiencing pain primarily in the low back area * Radicular component of pain has minimal effect on functionality, medication, quality of life * Experiencing low back pain for at least 3 months * Subject able to understand and provide informed consent * Comfortable and willing to accept random assignment to one of two study conditions (intervention or standard care condition) * Has an email account Exclusion Criteria: * Patients that do not own or have access to a smartphone or tablet * Has spinal instability, joint instability, or grade 2 or greater spondylolisthesis with instability * Primary symptoms due to spinal stenosis as evidenced by pseudoclaudication, leg weakness or numbness * Source of back pain related to an acute nerve impingement * Diagnosis of cancer/malignant tumors in the last 5 years * Source of back pain is an infection * History of spinal fusion surgery * Has a cardiac pacemaker, implanted defibrillator, spinal cord stimulator, pain pump, or any other implanted electronic device * Has had myocardial infarction within the past 6 months * Has had a coronary stent in the past 3 months * Has radicular pain symptoms that affect functionality, quality of life or medication intake * Has undergone surgery to solve pain related to the study indication in the past 12 months * Is scheduled for upcoming surgery to solve pain related to the study indication * History of opioid or drug use, or excessive alcohol use (excessive alcohol use defined as greater than 3 drinks a day on average), per investigator discretion * History of rheumatological or other inflammatory conditions such as rheumatoid arthritis, systemic lupus, erythematosus, etc. * Any psychiatric condition that may interfere with the study assessments or prevent the subject from complying with the requirements of the protocol, in investigator's judgment * Pregnant women (as determined by self-report) * Has a heart condition that limits the ability to do mild exercise due to symptoms such as fatigue, palpitations, shortness of breath, or chest pain * Has any health condition that limits the ability to do light-intensity exercise such as slow walking or light household chores * Diagnosed with dementia or a similar memory disorder * Has had a fall in the past three months * Unable to move from sitting to standing without help from another person * Unable to stand without assistance from another person or device * Any other disease, condition, or habit(s) that in the opinion of the Principal Investigator would interfere with study compliance or adversely affect study outcomes * Inability to complete data collection as required * No secondary/coinsurance or plans to change insurance from UHC in the next 3 months * Patients who were recommended spine surgery from a spine surgeon in the 3 months prior to the index month

Locations (1)

Optum Labs

Eden Prairie, Minnesota, United States