measurINg forceS durInG cHiropractic Treatment
Status: | Completed |
---|---|
Conditions: | Back Pain |
Therapuetic Areas: | Musculoskeletal |
Healthy: | No |
Age Range: | 18 - 65 |
Updated: | 4/21/2016 |
Start Date: | March 2015 |
End Date: | July 2015 |
measurINg forceS durInG cHiropractic Treatment (INSIGHT): A Single-Arm Clinical Case Series
The INSIGHT pilot study will measure forces applied by a doctor of chiropractic (DC) during
the delivery of a specific, manually based chiropractic treatment for participants with low
back pain.
the delivery of a specific, manually based chiropractic treatment for participants with low
back pain.
Low back pain (LBP) is a well-recognized health problem. One common manual therapy available
for the treatment of LBP is spinal manipulation (SM), which can be separated into 2
categories: High-Velocity Low-Amplitude (thrust) and Low-Velocity (non-thrust) SM according
to their force-delivery profiles. One commonly utilized non-thrust SM technique is the
Flexion-Distraction procedure. Several studies have reported manually applied forces during
thrust SM; however, the forces used during non-thrust SM, specifically those used with
Flexion-Distraction treatment are still unknown. The results of this pilot study will
provide preliminary information on treatment forces and sample size justification for future
full-scale trials, while also ascertaining the feasibility of the study protocol and patient
recruitment methods for such trials.
for the treatment of LBP is spinal manipulation (SM), which can be separated into 2
categories: High-Velocity Low-Amplitude (thrust) and Low-Velocity (non-thrust) SM according
to their force-delivery profiles. One commonly utilized non-thrust SM technique is the
Flexion-Distraction procedure. Several studies have reported manually applied forces during
thrust SM; however, the forces used during non-thrust SM, specifically those used with
Flexion-Distraction treatment are still unknown. The results of this pilot study will
provide preliminary information on treatment forces and sample size justification for future
full-scale trials, while also ascertaining the feasibility of the study protocol and patient
recruitment methods for such trials.
Inclusion Criteria:
- Able to demonstrate the necessary abilities (English language, literacy) needed to
provide informed consent without the assistance of another person (e.g., a proxy,
spouse, family member or other support person)
- Self-reported low back pain (acute, subacute or chronic) at the time of examination
and enrollment
Exclusion Criteria:
- Weight > 300lbs
- Spinal Pathology or conditions contraindicating study procedures or compromising
participant safety
- Inflammatory arthropathy involving the spine (e.g. Ankylosing spondylitis, Rheumatoid
arthritis)
- Spinal fracture in the past 6 months
- Other conditions requiring referral (e.g. self-reporting alcohol/substance dependence
or abuse, unstable spinal segments, and cauda equina syndrome)
- Pregnant or planning to become pregnant within the next 5 weeks
- Unable to tolerate study procedures safely
- Altered Mental Capacity
- Sensitivity to adhesives used in the study
- Uncontrolled hypertension
- Co-morbidity requiring simultaneous clinical management that compromises ability to
deliver study procedures or assess the participant's heath status or poses as a
scheduling burden
- Retention of legal advice or seeking a health-related insurance claim
- Compliance concerns (e.g. scheduling conflicts, moving from the quad city area,
unwilling to undergo required study procedures or receive treatment from study
doctor(s))
- Quebec Task Force Classification of 10 or 11: (chronic pain syndrome,
visceral/infectious source of LBP)
We found this trial at
1
site
Click here to add this to my saved trials