Postural Training Device (UPRIGHT) for Back Pain



Status:Not yet recruiting
Conditions:Back Pain, Back Pain
Therapuetic Areas:Musculoskeletal
Healthy:No
Age Range:18 - 65
Updated:10/14/2018
Start Date:February 1, 2020
End Date:February 1, 2022
Contact:Byron Schneider
Email:byron.j.schneider@vanderbilt.edu
Phone:615 875 5100

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Addition of Postural Training Device (UPRIGHT) to Routine Physical Therapy for the Treatment of Back Pain: a Randomized Trial

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

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.

Physical therapy will be completed 1-2 times per week over 4-6 weeks. If randomized to the
group that also receives a postural training device, one of the physical therapy sessions
will instruct the patient on use of the device, which can be used thereafter as tolerated by
the patient.

At 6 weeks and 3 months, questionnaires that assess patients pain and function will be
completed to assess outcomes

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
cord stimulator, bladder stimulator)

- Allergic skin reaction to tapes or adhesives

- Worker's compensation claim or legal action related to the thoracic or lumbar
pain

- Patients unable to read English and complete the assessment instruments

- Patients unable to attend assigned physical therapy sessions

- Incarcerated patients
We found this trial at
1
site
1211 Medical Center Dr
Nashville, Tennessee 37232
(615) 322-5000
Phone: 615-875-5100
Vanderbilt Univ Med Ctr Vanderbilt University Medical Center (VUMC) is a comprehensive healthcare facility dedicated...
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