- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01048749
Interventional Study of Effects on Spine Height With Two Unloading Positions
Immediate Changes in Spinal Height and Pain Following Aquatic Vertical Suspension in Patients With Low Back Pain and Signs of Nerve Root Compression
The purpose of this study is to test a physical therapy intervention for reducing pain in the low back and into the legs. With individuals over the age of 40 years, this pain may be associated to changes in back height from aging of the cushions between the back bones. When pain is caused from this, completion of different positions and rest periods have been shown to help reduce the pain, at least temporarily. This study will compare two such positions; 1)floating in deep warm water with weights attached to the ankles, to take the load off of the spine, 2)lying on their back with hip and knees flexed to a 90 degree angle. The height of each person will be measured before and after completion of each intervention using a specially designed measuring tool.
Experimental hypothesis:
- Subjects with low back and leg pain suggestive of nerve root compression syndrome will experience increase in spinal height when completing aquatic vertical suspension and/or land-based supine flexion.
- Subjects with low back and leg pain suggestive of nerve root compression syndrome will experience greater increase in height, greater reduction of pain intensity and location when completing underwater vertical suspension as compared to supine land based flexion.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Spinal height is affected throughout life from many different physiological changes and mechanical stresses, but a large portion is thought to occur primarily from intervertebral disc degeneration with resultant reduction in overall spinal height. The use of specific postures and rest periods to increase the overall spinal height has been suggested through various stadiometric research studies. This overall spinal height change can be used as a treatment tool for management of symptoms of chronic low back pain and signs of nerve root compression.
The purpose of the study is to investigate the effect of aquatic vertical suspension on spinal height, symptom location and pain intensity compared to a more commonly used land based supine flexion position.
The study will be conducted at one outpatient physical therapy clinic with subjects recruited from the local community.
A single blinded True Experimental Repeated Measure cross over design will be utilized.
Spine height will be measured using a commercially available stadiometer. Spinal height measurements will be completed after loaded walking, supine land based flexion positioning and after aquatic vertical hang.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Texas
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Cleburne, Texas, United States, 76033
- Cleburne Physical Therapy and Fitness Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- between the ages of 40-80 years,
- have current low back pain and/or numbness extending distal to the buttocks in the past 24 hours,
- pain level < 7/10 on the numerical rating scale, including symptom location change or pain intensity change with extension, lower limb weakness, achilles or patella reflex changes,
- reduction of lower limb sensation,
- positive SLR test.
Exclusion Criteria:
- inability to walk for a minimum of 15 minutes,
- inability to sit for a minimum of 5 minutes,
- inability to lie supine for a minimum of 15 minutes,
- fear of water or unwillingness to enter into a deep pool,
- allergy to chlorine,
- neurological disorders such as multiple sclerosis, spinal cord injury, incontinence, or spinal fusion,
- inability to elevate either shoulder above 90 degrees,
- pregnancy,
- vertebral fracture,
- pain level above 7/10 on the numeric pain scale or pain level reported at 0/10.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Active Comparator: aquatic vertical supsension
Spinal height measurement using a stadiometer following aquatic vertical suspension
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Subject is suspended in a warm water deep pool with two pool noodles around the subject and directly under the axilla.
Five pound weights are placed on the ankle and the subject maintains this unloaded position for 15 minutes.
Other Names:
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Active Comparator: land-based supine flexion condition
Spine height will be measured with a stadiometer following completion of the supine land-based flexion position.
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The subject will lay supine with the legs supported by a foam wedge with hips flexed to 90 degrees and knees flexed to 65 degrees.
They will maintain this unloaded position for 15 minutes.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Differences of change of spinal height following aquatic vertical suspension compared to lumbar supine flexion positioning.
Time Frame: Spine height is measured prior to and after each intervention and then statistical comparisons completed.
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Spine height is measured prior to and after each intervention and then statistical comparisons completed.
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Differences in pain intensity and location following aquatic vertical suspension compared to supine land-based flexion position.
Time Frame: Pain intensity and location measurements are taken prior to and after completion of each intervention
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Pain intensity and location measurements are taken prior to and after completion of each intervention
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Collaborators and Investigators
Investigators
- Study Chair: Jean M Brismee, PT, ScD, Texas Tech University Health Science Center
- Principal Investigator: Susanne M Simmerman, PT, BS, Texas Tech University Health Science Center
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- L08-144
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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