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:

  1. 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.
  2. 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

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

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Cleburne, Texas, United States, 76033
        • Cleburne Physical Therapy and Fitness Center

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

40 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
Active Comparator: aquatic vertical supsension
Spinal height measurement using a stadiometer following aquatic vertical suspension
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:
  • Physical Therapy Treatment
Active Comparator: land-based supine flexion condition
Spine height will be measured with a stadiometer following completion of the supine land-based flexion position.
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:
  • Physical Therapy Treatment

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
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.
Spine height is measured prior to and after each intervention and then statistical comparisons completed.

Secondary Outcome Measures

Outcome Measure
Time Frame
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
Pain intensity and location measurements are taken prior to and after completion of each intervention

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2008

Primary Completion (Actual)

June 1, 2009

Study Completion (Actual)

June 1, 2009

Study Registration Dates

First Submitted

January 12, 2010

First Submitted That Met QC Criteria

January 13, 2010

First Posted (Estimate)

January 14, 2010

Study Record Updates

Last Update Posted (Estimate)

January 14, 2010

Last Update Submitted That Met QC Criteria

January 13, 2010

Last Verified

January 1, 2010

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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