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Clinical Trials/NCT00837538
NCT00837538CompletedNot Applicable

A Comparison of Spinal Mouse® and X-ray Film to Measure a Instability of Lumbar Spine

Jyväskylä Central Hospital1 site in 1 country100 target enrollmentStarted: February 2009Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
Sagittal spinal range of motion
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The SpinalMouse is a computer-assisted medical device that measures and graphically reports on posture and range of motion of the axial spine. The data has shown to be highly valid and reproducible while compared to x-ray film. The aim of the study is to evaluate if the Spinal Mouse is a reliable clinical diagnostic device to screen those patients having instability in the lumbar area.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •supposed instability of lumbar spine

Exclusion Criteria

  • •not willing to participate to study

Outcomes

Primary Outcomes

Sagittal spinal range of motion

Time Frame: One measurement before or after x-ray film

Secondary Outcomes

  • Pain; pain drawing, VAS(Once in the same day with range of motion measurements)
  • Oswestry Disability Questionnaire(Once in the same day with range of motion measurements)
  • Questionnaire; socio-demographic variables, back/leg trouble history(Once in the same day with range of motion measurements)

Investigators

Sponsor
Jyväskylä Central Hospital
Sponsor Class
Other

Study Sites (1)

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