Clinical Outcomes in Chronic Low Pain Back Utilizing Activity Trackers

This is a randomized controlled study to assess the effects of activity monitors, with
telehealth follow ups, on the treatment of chronic low back pain subjects. Subjects with low
back pain will present for evaluation to the NYIT Academic Health Care Center. Once serious
complications have been ruled out and a diagnosis of chronic low back pain has been made,
subjects will be informed about this proposed study and asked if they would like to
participate. Voluntary subjects will then be consented by designated investigators. The
subjects will then be randomized into either the activity tracker and telemedicine follow up
group or the control group.

Once enrolled, all subjects will complete the study as outlined in the procedures. It will
involve the use of several validated assessment tools. Following the initial visit, subjects
in both groups will return in 6 weeks for reassessment. Subjects in the experimental group
will additionally be given an activity tracker and have 2 telemedicine visits at 2 and 4
weeks.

Inclusion Criteria:

- Subject is at least 18 years age and younger than 75 years of age

- Subjects evaluated and found to have low back lasting longer than 3 months

Exclusion Criteria:

The subject suffers from any of the following:

- Foot drop

- Recent diagnosis of malignancy

- Recent infection

- Saddle anesthesia

- Urinary or bowel incontinence

- Progressive neuromotor or sensory loss

- The subject is unable to complete the assessment tools

- The subject is pregnant