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Chiropractic Prone Distraction for Lower Back Pain

Primary Purpose

Herniated Disc, Lower Back Pain, Sciatica

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Prone Distraction
Side-Posture Manipulation
Side-Posture Manipulation & Prone Distraction
Usual Care (Control Group)
Sponsored by
Samueli Institute for Information Biology
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Herniated Disc

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Active Duty military personnel Aged 18-45 (age is limited to 45 years due to the natural aging and degeneration of the discs; the less hydration the disc maintain, the less likely manipulation will be successful). Have subacute low back pain (more than three months duration but less than six months duration), with radicular component (sciatica) rated at a minimum level of 4 on the Numerical Rating Scale (NRS) of the Brief Pain Inventory Have a confirmed herniated disc, as noted on MRI, which correlates with the clinical findings (sciatica) In this study, a "herniated disc" refers to any localized displacement of disc material, including nucleus, cartilage, fragmented apophyseal bone, or fragmented anular tissue, which results in back and leg pain. "Herniated Disc" also will include disc extrusions and disc bulges (protrusions) only when with associated annular tears. In this study, "sciatica" refers to pain in the lower extremity/ies that follows the course of the sciatic nerve Exclusion Criteria: Patients who are not able to give informed consent. Pregnant or nursing women Patients who have a primary bone disease, cancer, infection, spondylolysis or spondylolisthesis. Patients who have had prior spine surgery, including rhizotomy Participation in another conflicting research study Patients who cannot commit to a trial lasting up to eight weeks or cannot come for bi-weekly treatments Patients who are going through a course of physical therapy or chiropractic treatment or at the time of planned enrollment or are being currently being managed and/or treated for any pain condition Patients who have an unstable medical or psychiatric condition Patients who are planning or have been advised to have spine surgery Any contraindications to either prone distraction or side posture manipulation will disqualify potential subjects from any participation in this study Patients with a pacemaker.

Sites / Locations

  • National Naval Medical Center

Outcomes

Primary Outcome Measures

Change in overall leg pain intensity, as assessed by the change, if any, of leg pain documented on the Numerical Rating Scale (NRS) in the Brief Pain Inventory (BPI) from baseline to 8 weeks
Time to pain relief, defined as NRS less than 4 after 2 consecutive visits

Secondary Outcome Measures

Change in overall back pain intensity, as assessed by the change, if any, of back pain documented on the BPI from baseline to 8 weeks
Change in overall pain intensity, as assessed by the change, if any, of the sum of back and leg pain documented on the BPI at measured intervals
Change in overall pain intensity, as assessed by the change, if any, of the sum of back and leg pain documented on the BPI from baseline to 8 weeks
Patient satisfaction with treatment, as assessed by The Client Satisfaction Questionnaire
Medication use, as assessed by the Medication Log
Functional disability, as assessed by The Roland-Morris Low Back Pain and Disability Questionnaire
Lost/decreased workdays
Change, if any, in percent of disc herniation, as determined by the study neuroradiologist
Descriptive changes in disc morphology, as assessed by the study neuroradiologist
Variability of treatment, as assessed by the number or prescriptions written, the number of visits to the Primary Care Clinic, as well as the number of referrals to additional treatments outside of the chiropractic clinic

Full Information

First Posted
December 21, 2005
Last Updated
May 7, 2008
Sponsor
Samueli Institute for Information Biology
Collaborators
National Naval Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT00269503
Brief Title
Chiropractic Prone Distraction for Lower Back Pain
Official Title
A Pilot Study of Chiropractic Prone Distraction for Subacute Back Pain With Sciatica
Study Type
Interventional

2. Study Status

Record Verification Date
May 2008
Overall Recruitment Status
Terminated
Study Start Date
March 2006 (undefined)
Primary Completion Date
June 2006 (Actual)
Study Completion Date
June 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Samueli Institute for Information Biology
Collaborators
National Naval Medical Center

4. Oversight

5. Study Description

Brief Summary
Back pain is a major cause of disability in the United States. The lifetime prevalence of low back pain is estimated at 60-90%. Back pain has conservatively been estimated to involve total direct and indirect costs of over $25 billion annually in lost wages, treatment, and related issues. These losses clearly extend to the active duty population cared for by military health care facilities. Chiropractic medicine is characterized by the use of a number of physical manipulations and mobilization techniques, which can be used singly or in combination to treat a variety of medical conditions. Although basic clinical practice guidelines for Chiropractic have been developed, few studies have rigorously compared techniques and their outcomes for specific conditions. Fewer still have sought to correlate treatment modality with both anatomical effect and clinical outcome. Throughout the military, Chiropractic care is available only to active duty personnel and only at a limited number of medical treatment facilities. At National Naval Medical Center, it is a well-established treatment option, where the full array of techniques is employed, primarily for painful conditions, and most often for back pain. This study seeks to clarify the mechanisms of action and efficacy of one specific treatment option, prone distraction, for the relief of subacute sciatica due to radiographically confirmed herniated disc, and to compare it to side-posture manipulation and standard medical management. Prone lumbar distraction utilizes a specialized table with motorized continual motion distraction. This table has multiple mechanical articulations that can be used to place patients in a wide variety of positions. Patients being treated with continuous motion distraction are placed prone with the table positioned for maximum comfort and centralization of symptoms. Side posture manipulation is a widely practiced, standard chiropractic technique, which has been shown to provide considerable clinical improvement for patients with sciatica. Low- grade oscillatory stresses are performed within the physiological range of normal joint motion. The hip, pelvis and lumbar spine are rotated forward with manual pressure while a counter rotation of the chest and thoracic spine is applied.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Herniated Disc, Lower Back Pain, Sciatica

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Prone Distraction
Intervention Type
Procedure
Intervention Name(s)
Side-Posture Manipulation
Intervention Type
Procedure
Intervention Name(s)
Side-Posture Manipulation & Prone Distraction
Intervention Type
Procedure
Intervention Name(s)
Usual Care (Control Group)
Primary Outcome Measure Information:
Title
Change in overall leg pain intensity, as assessed by the change, if any, of leg pain documented on the Numerical Rating Scale (NRS) in the Brief Pain Inventory (BPI) from baseline to 8 weeks
Title
Time to pain relief, defined as NRS less than 4 after 2 consecutive visits
Secondary Outcome Measure Information:
Title
Change in overall back pain intensity, as assessed by the change, if any, of back pain documented on the BPI from baseline to 8 weeks
Title
Change in overall pain intensity, as assessed by the change, if any, of the sum of back and leg pain documented on the BPI at measured intervals
Title
Change in overall pain intensity, as assessed by the change, if any, of the sum of back and leg pain documented on the BPI from baseline to 8 weeks
Title
Patient satisfaction with treatment, as assessed by The Client Satisfaction Questionnaire
Title
Medication use, as assessed by the Medication Log
Title
Functional disability, as assessed by The Roland-Morris Low Back Pain and Disability Questionnaire
Title
Lost/decreased workdays
Title
Change, if any, in percent of disc herniation, as determined by the study neuroradiologist
Title
Descriptive changes in disc morphology, as assessed by the study neuroradiologist
Title
Variability of treatment, as assessed by the number or prescriptions written, the number of visits to the Primary Care Clinic, as well as the number of referrals to additional treatments outside of the chiropractic clinic

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Active Duty military personnel Aged 18-45 (age is limited to 45 years due to the natural aging and degeneration of the discs; the less hydration the disc maintain, the less likely manipulation will be successful). Have subacute low back pain (more than three months duration but less than six months duration), with radicular component (sciatica) rated at a minimum level of 4 on the Numerical Rating Scale (NRS) of the Brief Pain Inventory Have a confirmed herniated disc, as noted on MRI, which correlates with the clinical findings (sciatica) In this study, a "herniated disc" refers to any localized displacement of disc material, including nucleus, cartilage, fragmented apophyseal bone, or fragmented anular tissue, which results in back and leg pain. "Herniated Disc" also will include disc extrusions and disc bulges (protrusions) only when with associated annular tears. In this study, "sciatica" refers to pain in the lower extremity/ies that follows the course of the sciatic nerve Exclusion Criteria: Patients who are not able to give informed consent. Pregnant or nursing women Patients who have a primary bone disease, cancer, infection, spondylolysis or spondylolisthesis. Patients who have had prior spine surgery, including rhizotomy Participation in another conflicting research study Patients who cannot commit to a trial lasting up to eight weeks or cannot come for bi-weekly treatments Patients who are going through a course of physical therapy or chiropractic treatment or at the time of planned enrollment or are being currently being managed and/or treated for any pain condition Patients who have an unstable medical or psychiatric condition Patients who are planning or have been advised to have spine surgery Any contraindications to either prone distraction or side posture manipulation will disqualify potential subjects from any participation in this study Patients with a pacemaker.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William E Morgan, DC
Organizational Affiliation
National Naval Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
CDR Robert E Rosenbaum, MC, USN
Organizational Affiliation
National Naval Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
National Naval Medical Center
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20889
Country
United States

12. IPD Sharing Statement

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Chiropractic Prone Distraction for Lower Back Pain

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