Phase
Condition
Chronic Pain
Treatment
N/AClinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Mechanical (myofascial), axial back pain (focused around the spine)
6/10 or greater level of pain
Functionally debilitated by their pain (e.g., difficulty walking)
Minimal radicular symptoms with no effect on functionality, medication, quality oflife
Expressed desire to stop taking pain medications
Expressed desire to improve disability
80% or greater of disability is due to pain in the low back (as opposed to other bodyareas)
Experiencing chronic pain for at least 6 months
Interested in being active, improving their functionality
Comfortable with using technology in daily life
Subject able to understand and grant informed consent
Documented adherence with clinic follow up visits per medical records
Has an email account
Above 18 years old
Exclusion
Exclusion Criteria:
Patients that do not own or have access to a smartphone
Has spinal instability, joint instability, or grade 2 or greater spondylolisthesiswith instability
Primary symptoms due to spinal stenosis
Source of back pain related to an acute nerve impingement
Diagnosis of cancer/malignant tumors in the last 5 years
Source of back pain is an infection
Source of pain is a prior spinal fusion surgery
Has a cardiac pacemaker, implanted defibrillator or other implanted electronic device
Has radicular pain symptoms that affect functionality, quality of life or medicationintake
Has undergone surgery to solve pain related to the study indication in the past 6months
Patients with history of opioid, alcohol or drug abuse in the last 5 years, perinvestigator discretion
Any psychiatric condition that may interfere with the study assessments or prevent thesubject from complying with the requirements of the protocol, in the judgement of theinvestigator
Inability to complete subjective data as required; e.g. on mobile application andquestionnaires
Pregnant women (as determined by self-report)
Have severe epilepsy
Have severe form of cardiovascular disease
Any other disease, condition, or habit(s) that in the opinion of the PrincipalInvestigator would interfere with study compliance or adversely affect study outcomes
Study Design
Study Description
Connect with a study center
Clinical Trials Research
Lincoln, California 95648
United StatesSite Not Available
Superior Research
Sacramento, California 95831
United StatesSite Not Available
University of California Medical Center
San Francisco, California 94143
United StatesActive - Recruiting
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