Slump Sitting X-ray of the Lumbar Spine Is Better Than Conventional Flexion View

September 9, 2015 updated by: Orthosurgery, National University Hospital, Singapore

Slump Sitting X-ray of the Lumbar Spine Is Better Than Conventional Flexion

This is a prospective, single-blinded, randomized-controlled study comparing a new method (slump-sitting) with the conventional method (forward erect bending) of performing lumbar spine flexion X-rays.

Study Overview

Detailed Description

Power calculation was performed based on preliminary pilot results using a clinically set difference of 10 degrees (SD 15 degrees) change in mean global lumbar spine flexion between sitting and standing postures. An estimated sample population of 100 patients was deemed necessary for this study to fulfill a statistical power of 90% and a two-sided 5% significance level.

Block randomization of every 4 subjects was performed at the beginning of the study to ensure equal numbers of subjects in both study arms for comparison and these results were concealed in envelopes.

During the clinical consult, history taking was performed as per a usual clinic visit. Specific patient's details including age, occupation, presence and severity of back pain, presence and severity of leg pain, and neurological symptoms were documented. Physical examination was performed accordingly and parameters such as clinical range of motion of the lumbar spine, neurological signs and provocative tests were recorded for later analysis.

For the flexion radiographs, both the new and conventional methods were performed on each patient. These pictures were made into charts and visually displayed. They serve as instructional manuals for patients during the radioimaging process, which are again reinforced with verbal instructions from the on-duty radiographers.

Both images were done with the X-ray beam projected from the patients's left and at a distance of 100cm from the patient. The central beam was directed at the estimated centre of L3, with T11 vertebral body and mid-body of the sacrum serving as superior and inferior limits respectively. A single extension view of the lumbar spine was also performed after these flexion views. All radiographs were stored on Digital Imaging and Communications in Medicine (DICOM) format and viewed with Centricity Enterprise Web V3.0 (8.0.1400.128) for assessment.

Measurements were done by 2 independent reviewers and an average of their readings was recorded. Both reviewers were blinded to the method in which flexion X-rays was taken.

Interim data analysis is planned at 30th patient and the 60th patient. During this time point, the primary objective which look at mean global lumbar spine flexion between sitting and standing postures is assessed.

All collected data and measurements were tabulated using Microsoft Excel 2011(Version 14.0 (32-bit)) and analyzed using International Business Machines (IBM) Statistical Package for the Social Sciences (SPSS Version 23.0).

For the main analysis of both global and segmental lumbar flexion, as well as the measured displacements obtained between the two flexion methods, paired t-test was employed.

There is no requirement to follow up the patients in this study. The whole study is to be completed within 1 year of recruitment

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

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

45 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patients above 45 years of age;
  • With mechanical low back pain,
  • With spondylolisthesis
  • Physically able to position themselves correctly for both methods of X-rays

Exclusion Criteria:

  • Previous spinal interventions
  • Suspected findings for spinal malignancies, spinal trauma, and inflammatory spinal diseases
  • Pregnant women

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: Diagnostic
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Slump sitting
Slump sitting flexion of lumbar spine
Patients are asked to sit slumped on the chair as much as possible without leaning forwards, and place you hands below your thighs.
Active Comparator: Forward bending
Forward erect bending of lumbar spine
Patients are asked to stand with both feet placed together, hands behind their heads, and bend forward in this position as much as possible without falling

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Global lumbar spine flexion range of motion
Time Frame: Day 1 (no follow-up, outcome assessed immediately)
Change in mean global lumbar spine flexion between sitting and standing postures
Day 1 (no follow-up, outcome assessed immediately)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Segmental lumbar spine flexion range of motion
Time Frame: Day 1 (no follow-up, outcome assessed immediately)
Change in segmental global lumbar spine flexion between sitting and standing postures
Day 1 (no follow-up, outcome assessed immediately)
Segmental translational changes during lumbar spine flexion
Time Frame: Day 1 (no follow-up, outcome assessed immediately)
Percentage translation at each segmental lumbar spine levels
Day 1 (no follow-up, outcome assessed immediately)

Collaborators and Investigators

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

Investigators

  • Study Chair: Hee-Kit Wong, MBBS, National University Health System

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

May 1, 2014

Primary Completion (Actual)

May 1, 2015

Study Completion (Actual)

May 1, 2015

Study Registration Dates

First Submitted

August 20, 2015

First Submitted That Met QC Criteria

September 9, 2015

First Posted (Estimate)

September 11, 2015

Study Record Updates

Last Update Posted (Estimate)

September 11, 2015

Last Update Submitted That Met QC Criteria

September 9, 2015

Last Verified

September 1, 2015

More Information

Terms related to this study

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.

Clinical Trials on Low Back Pain

Clinical Trials on Slump sitting

Subscribe