Clinician Satisfaction With the VERABAND™

Recruiting now · Not applicable

Conditions studied: Chronic Low-back Pain

In brief

The VERABAND™ is a newly-developed, disposable, wearable activity monitor. The researchers will assess clinician satisfaction with the usability and likelihood of clinical adoption of the newly-developed, disposable, wearable activity monitor, across multiple clinical sites in the chronic low back pain (cLBP) population.

Key facts

Study ID

NCT06080464

Run by

University of Michigan

People needed

360

Starts

2025-06-09

Expected to finish

2027-06-01

Last updated by the study team

2026-06-03

Who can join

Age: 18 and older, up to 85. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Ambulatory
• Diagnosis of chronic low back pain (cLBP) according to the criteria of National Institute of Health (NIH) Task Force on Research Standards for cLBP
• Answering 'Yes' to the question: Does your low back pain interfere with your mobility?
• Starting any new non-surgical treatment or combination of treatments for cLBP as part of their normal ongoing care, including medications; physical therapy/exercise; integrated therapies (e.g., massage, acupuncture, yoga); cognitive- behavioral therapy; and/or interventional procedures (e.g., epidural steroid or facet joint injections)
• Willingness to wear a VERABAND™ continuously until their next clinic visit and return used devices in the mail.

You may not qualify if…

• Clinical findings suggesting the presence of ongoing systemic disease, including fever, weight loss, initiation of pain following major trauma, immunosuppression, intravenous drug use, recent bacterial infection, severe or persistent sensory or motor involvement of bowel, bladder, or lower extremity; or any condition that would greatly limit physical activity not due to pain.
• Inability to speak and write English.
• Visual or hearing difficulties that would preclude participation.
• Severe psychiatric disorders that in the opinion of the investigative team would interfere with participation in the study. This includes any active suicidal ideations or history of suicide attempts. Exclusions will be based on self-reported medical history or chart review and in accordance with Diagnostic and Statistical Manual of Mental Disorders (DSM)-5 criteria.
• Individuals receiving disability or compensation or involved in litigation.
• Scheduled surgery before follow-up.

Where it is running

• University of Kansas Medical Center — Kansas City, Kansas, United States (enrolling)
• University of Michigan — Ann Arbor, Michigan, United States (enrolling)
• Altman Clinical and Translational Research Institute — La Jolla, California, United States

Full record on ClinicalTrials.gov

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