N/A Completed N=30 Randomized Single-blind Supportive Care

Upright Back Posture Device Study

Back Pain · Postural Low Back Pain · Lower Back Pain

Source: ClinicalTrials.gov NCT03769246 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Jul 2024

Primary outcomePrimary: Score on Numeric Pain Rating Scale (NPRS) — 2.54; 2.44; 1.75; 1.49 score on a scale

Summary

This is a randomized controlled study to determine if patients between the ages of 18-50 years, with posture related low back pain, who use the Upright device demonstrate improved pain control and self perception of posture compared to those given standard ergonomic instruction.

Outcome Measures

Outcome	Result	p-value
PRIMARY Score on Numeric Pain Rating Scale (NPRS)	2.54; 2.44; 1.75; 1.49	—
PRIMARY Score on the PROMIS Pain Interference Short Form 6b	2.40; 2.53; 1.85; 1.60; 2.27; 2.47	—

Eligibility Criteria

Inclusion Criteria

Postural-related back pain

Exclusion Criteria

A diagnosis of significant scoliosis, herniated/bulging disc, lumbar spondylolysis, radiculitis, facet arthrosis, fibromyalgia, rheumatoid arthritis, seronegative spondyloarthropathy.
Neurologic deficits on exam
Currently in physical therapy (PT)

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03769246). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.