Clinician Satisfaction With the VERABAND™

Conditions

• Chronic Low-back Pain

Eligibility Criteria

Sex

ALL

Age

18 Years - 85 Years

Healthy Volunteers

Not accepted

Interventions

• VERABAND information — OTHER
  The device, VERABAND™, activity data reports (including a summary broken down by week) will be provided to treating clinicians prior to each patient's follow-up clinic visit.

Study Details

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 Dates

Start date

Jun 9, 2025

Status verified

Jun 2026

Primary completion

Dec 31, 2026

Completion

Jun 30, 2027

Study Design

Enrollment

360 participants (estimated)

Allocation

NA

Intervention model

SINGLE_GROUP

Primary purpose

HEALTH_SERVICES_RESEARCH

Arms

• Experimental: VERABAND information
  Consented patient participants will be given a VERABAND™ activity monitor during an initial clinic visit (baseline) and will then be tracked longitudinally after beginning a new pain treatment regime as part of their normal ongoing care. VERABAND™ activity data reports (including a summary broken down by week) will subsequently be provided to treating clinicians prior to each patient's follow-up clinic visit. The arm is all of the clinicians of the participants.

Primary Outcome Measure

Measure clinician satisfaction of the usability of the VERABAND™ using the System Usability Scale (SUS) [ Time Frame: approximately 7 weeks ]

Central Contacts

• Kristi Pickup, MSW
  734-764-4072
  [email protected]

Locations (3)

Find similar trials in La Jolla, CA

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