Actively Recruiting
Clinician Satisfaction With the VERABAND™
Led by University of Michigan · Updated on 2026-03-25
360
Participants Needed
3
Research Sites
103 weeks
Total Duration
On this page
Sponsors
U
University of Michigan
Lead Sponsor
N
National Institute of Neurological Disorders and Stroke (NINDS)
Collaborating Sponsor
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Clinician Satisfaction With the VERABAND™
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Ambulatory patients
- Diagnosis of chronic low back pain (cLBP) according to NIH criteria
- Low back pain that interferes with mobility
- Starting any new non-surgical treatment for cLBP as part of normal care
- Willingness to wear the VERABAND174 device continuously until next clinic visit and return it by mail
You will not qualify if you...
- Signs of ongoing systemic disease such as fever, weight loss, recent infection, or severe sensory/motor problems not caused by pain
- Inability to speak and write English
- Visual or hearing difficulties that prevent participation
- Severe psychiatric disorders including active suicidal thoughts or past suicide attempts
- Receiving disability benefits, compensation, or involved in litigation
- Scheduled surgery before follow-up
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Altman Clinical and Translational Research Institute
La Jolla, California, United States, 92037
Not Yet Recruiting
2
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Not Yet Recruiting
3
University of Michigan
Ann Arbor, Michigan, United States, 48109
Actively Recruiting
Research Team
K
Kristi Pickup, MSW
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
1
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