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Effectiveness of Mechanical Decompression for Low Back Pain Relief (SpiDERS)

Primary Purpose

Low Back Pain

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
SpineMed Table, Cert HealthSciences LLC
SpineMed Table, Cert HealthSciences LLC
Sponsored by
State University of New York - Upstate Medical University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Back Pain focused on measuring Low Back Pain

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Non-specific LBP of at least 6 weeks duration with no evidence of underlying disease or anatomic abnormalities,
  • Applicants may have pain radiating to their legs.

Exclusion Criteria:

  • Any episode of Acute LBP within the last 6 weeks or less
  • Recent Fractures, less than 8 weeks of any bone
  • Tumors of any type including soft tissue tumors, myeloma, malignant or documented tumors of any type
  • Gross osteoporosis,
  • Spondylolisthesis grade 2 and above,
  • Hardware fixation, spine fixation or other boney fusion
  • Obesity as defined by a BMI greater than 35, body weight over 287 pounds,
  • Contra-indication for MRJ assessment,
  • Pregnancy,
  • neurologic deficits,
  • bowel or bladder incontinence,
  • progressive lower extremity weakness,
  • need for narcotic pain medications for other conditions.

Sites / Locations

  • SUNY Upstate Medical University

Arms of the Study

Arm 1

Arm 2

Arm Type

Sham Comparator

Experimental

Arm Label

B

A

Arm Description

Group B will receive sham decompression treatment (i.e. tension not exceeding 15 lbs) for 30 minutes and ice treatment for 15 minutes once a day during each treatment session. No incremental increases will be used for Group B.

For Group A (the treated group) the following tension adjustments will be used: starting treatment tension will equal 1/4 body weight minus 10 lbs. Incremental increases of 4 lbs. per session will be implemented until optimum tensions are reached, which would be a maximum of ¼ body weight plus 25 lbs, unless distraction tensions cause discomfort, which would require a reduction of the tensions applied.

Outcomes

Primary Outcome Measures

Pain will be measured using a 0-100 visual analog scale.
Functional activity will be measured using the Roland Morris activity scale
MRI outcome measures include thickness of disc (disc height, intervertebral space), extent of disc bulging, intervertebral alignment.

Secondary Outcome Measures

Physical and social activities and quality of life will be measured with the COOP
Functional health will be measured with the SF-36
Depression will be measured using the Geriatric Depression Scale (GDS)
Treatment satisfaction will be measured using a 5-point Likert scale.
Reduction in pain medication usage

Full Information

First Posted
June 20, 2008
Last Updated
October 14, 2016
Sponsor
State University of New York - Upstate Medical University
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1. Study Identification

Unique Protocol Identification Number
NCT00704210
Brief Title
Effectiveness of Mechanical Decompression for Low Back Pain Relief
Acronym
SpiDERS
Official Title
Effectiveness of Mechanical Decompression for Low Back Pain Relief
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Withdrawn
Why Stopped
Study withdrawn by sponsor
Study Start Date
August 2006 (undefined)
Primary Completion Date
December 2008 (Anticipated)
Study Completion Date
July 2009 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
State University of New York - Upstate Medical University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Objective To demonstrate the effectiveness of a conservative treatment approach for chronic low back pain that addresses the underlying problem of intervertebral disc lesions and degenerative disc disease, namely vertebral pressure on vital structures of the lumbar region.
Detailed Description
Low back pain (LBP) is a common medical problem and a challenging condition to treat. This study will investigate the effectiveness of a conservative treatment approach for chronic LBP. To this point few treatment approaches specifically address the resolution of underlying pathologies leading to a high probability of recurrence of LBP. Further, current treatment options for lumbar disc pathology have been of limited demonstrated effectiveness. The purpose of this study is to determine whether a non-surgical therapeutic approach designed to effect intervertebral widening and allow for reduction of disc protrusion will reduce patients' pain and improve their activity levels. The study will assess whether a computer-assisted traction treatment [decompression] protocol results in improvement in patient pain levels and daily activity levels. Further, to determine if such treatment results in intervertebral widening and reduction of any disc protrusions as demonstrated by direct imaging of the lumbar spine. A double-blind (treatment vs. sham treatment) design will be employed Specific Aims To study the effectiveness of decompression therapy for LBP patients with lumbar disc herniation and degenerative disc problems. To demonstrate that decompression therapy for LBP patients results in a demonstrated reduction in levels of reported pain. To demonstrate that decompression therapy for LBP patients results in a demonstrated greater return to daily activities. To demonstrate that decompression therapy for LBP patients results in increased intervertebral space and reduced disk protrusion (if present) as measured by MRI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain
Keywords
Low Back Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
B
Arm Type
Sham Comparator
Arm Description
Group B will receive sham decompression treatment (i.e. tension not exceeding 15 lbs) for 30 minutes and ice treatment for 15 minutes once a day during each treatment session. No incremental increases will be used for Group B.
Arm Title
A
Arm Type
Experimental
Arm Description
For Group A (the treated group) the following tension adjustments will be used: starting treatment tension will equal 1/4 body weight minus 10 lbs. Incremental increases of 4 lbs. per session will be implemented until optimum tensions are reached, which would be a maximum of ¼ body weight plus 25 lbs, unless distraction tensions cause discomfort, which would require a reduction of the tensions applied.
Intervention Type
Device
Intervention Name(s)
SpineMed Table, Cert HealthSciences LLC
Intervention Description
For Group A (the treated group) the following tension adjustments will be used: starting treatment tension will equal 1/4 body weight minus 10 lbs. Incremental increases of 4 lbs. per session will be implemented until optimum tensions are reached, which would be a maximum of ¼ body weight plus 25 lbs, unless distraction tensions cause discomfort, which would require a reduction of the tensions applied.
Intervention Type
Device
Intervention Name(s)
SpineMed Table, Cert HealthSciences LLC
Intervention Description
Group B will receive sham decompression treatment (i.e. tension not exceeding 15 lbs) for 30 minutes and ice treatment for 15 minutes once a day during each treatment session. No incremental increases will be used for Group B.
Primary Outcome Measure Information:
Title
Pain will be measured using a 0-100 visual analog scale.
Time Frame
19 weeks
Title
Functional activity will be measured using the Roland Morris activity scale
Time Frame
19 weeks
Title
MRI outcome measures include thickness of disc (disc height, intervertebral space), extent of disc bulging, intervertebral alignment.
Time Frame
19 weeks
Secondary Outcome Measure Information:
Title
Physical and social activities and quality of life will be measured with the COOP
Time Frame
19 weeks
Title
Functional health will be measured with the SF-36
Time Frame
19 weeks
Title
Depression will be measured using the Geriatric Depression Scale (GDS)
Time Frame
19 weeks
Title
Treatment satisfaction will be measured using a 5-point Likert scale.
Time Frame
19 weeks
Title
Reduction in pain medication usage
Time Frame
19 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Non-specific LBP of at least 6 weeks duration with no evidence of underlying disease or anatomic abnormalities, Applicants may have pain radiating to their legs. Exclusion Criteria: Any episode of Acute LBP within the last 6 weeks or less Recent Fractures, less than 8 weeks of any bone Tumors of any type including soft tissue tumors, myeloma, malignant or documented tumors of any type Gross osteoporosis, Spondylolisthesis grade 2 and above, Hardware fixation, spine fixation or other boney fusion Obesity as defined by a BMI greater than 35, body weight over 287 pounds, Contra-indication for MRJ assessment, Pregnancy, neurologic deficits, bowel or bladder incontinence, progressive lower extremity weakness, need for narcotic pain medications for other conditions.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William D Grant, EdD
Organizational Affiliation
State University of New York - Upstate Medical University
Official's Role
Principal Investigator
Facility Information:
Facility Name
SUNY Upstate Medical University
City
Syracuse
State/Province
New York
ZIP/Postal Code
13210
Country
United States

12. IPD Sharing Statement

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Effectiveness of Mechanical Decompression for Low Back Pain Relief

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