Postural Training Device (UPRIGHT) for Back Pain (NCT03449160) | Clinical Trial Compass
WithdrawnNot Applicable
Postural Training Device (UPRIGHT) for Back Pain
Stopped: COVID 19 which is preventing outpatient and elective procedures
United States0Started 2020-05-01
Plain-language summary
Participants with low back pain who are referred for physical therapy will be randomized to routine physical therapy or routine physical therapy plus receiving a postural training device
Who can participate
Age range18 Years – 65 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Age 18 - 65, capable of understanding and providing consent in English, capable of complying with the outcome instruments used, and capable of attending all planned therapy sessions
* Primary complaint of lumbar or thoracic pain thought to be at least in part due to mechanical/postural etiologies based on clinical presentation
* 7 day average numeric pain rating score (NPRS) of at least 4 on a 0-10 scale at baseline evaluation
* Pain duration of at least 2 months
* Patient owns and is familiar with the use of a personal smart phone
* Patient consents to treatment with postural based physical therapy. In order to maintain blinding, patients will not be provided with details of the treatment plan until after the randomization process has been performed. They will only be informed of the treatment protocol for the group to which they have been assigned.
Exclusion Criteria:
* \*History of prior thoracic or lumbar fusion surgery
* Acute Spine fracture
* Current pregnancy
* BMI over 40
* Inability to sense UPRIGHT vibration
* Active Systemic inflammatory arthritis (e.g. rheumatoid arthritis, ankylosing spondylitis, lupus)
* Medical conditions causing significant functional disability (e.g. stroke, spinal cord injury, amputation)
* Severe Chronic widespread pain or somatoform disorder (e.g. fibromyalgia)
* Severe clinical depression, or psychotic features
* Implanted electrical medical device (i.e. cardiac pacemaker/defibrillator, spinal c…
What they're measuring
1
Improvement/Change in Pain
Timeframe: Primary outcome is at 6 weeks, secondary time point 12 weeks