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Clinical Trials/NCT07557186
NCT07557186Not yet recruitingNot Applicable

Validity and Reliability of Kinovea Software Program Measurement of Lumbar Extensibility Using Modified-Modified Schober Test

Cairo University1 site in 1 country100 target enrollmentStarted: January 1, 2027Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
100
Locations
1
Primary Endpoint
Validity of Kinovea Software Measurement

Study Overview

Brief Summary

This study will be conducted to determine the validity and reliability of Kinovea Software measurement of lumbar extensibility using Modified-Modified Schober Test

Detailed Description

Reduced lumbar mobility has been associated with various musculoskeletal alterations, including low back pain, changes in movement patterns, and increased risk of spinal disorders. Lumbar range of motion is considered a crucial parameter in determining disability for compensation claims and litigation worldwide.

The Modified-Modified Schober Test (MMST) is a widely used clinical tool for assessing lumbar range of motion, particularly flexion. This test utilizes the posterior superior iliac spines (PSIS) as the lower anatomical landmark and a point 15 cm above as the upper landmark, measuring the increase in distance during forward flexion.

Despite some limitations, the MMST remains a recommended clinical tool due to its simplicity and established reliability.

Regarding extensibility measurement, recent research has demonstrated that Kinovea software exhibits excellent intra-rater reliability, excellent inter-rater reliability, and strong criterion validity for measuring hamstring extensibility using the sit and reach test when compared to traditional tape measurements.

Therefore, this study aims to fill this research gap by measuring the validity & reliability of Kinovea software program in measuring lumbar extensibility using the Modified-Modified Schober Test by examining the psychometric properties of Kinovea for lumbar spine assessment as the kinovea software is low cost, provide more accurate data and easy to use.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 25 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • The subjects' ages range from 18 to 25 years old.
  • Subjects from both genders.
  • Body mass index: 18-24.9 Kg/m2
  • Waist-Hip ratio: Male: 0.9 to 1, Female: 0.85

Exclusion Criteria

  • The following subjects will be excluded from the study patients with:
  • Lumber Disc prolapse.
  • Spinal fixation.
  • Spinal deformities like scoliosis and kyphosis.
  • Hamstring injury.
  • Hip, knee and ankle orthopedic problems.
  • Shoulders, Elbow and Wrist orthopedic problems.
  • Athletes.
  • Pregnant woman.
  • Subject takes any muscle relaxant.

Arms & Interventions

Normal Subjects

Normal participants will be participated, their lumbar extensibility will be measured through the Modified-Modified Schober Test, concurrently will be captured by a video camera. Each video for every subject will be downloaded onto a computer, followed by analysis using Kinovea software to evaluate criterion validity.

Outcomes

Primary Outcomes

Validity of Kinovea Software Measurement

Time Frame: 1 year

To evaluate criterion validity the trials of Modified-Modified Schober test will be concurrently captured by a video camera. Each video underwent downloading onto a computer, followed by analysis using Kinovea software and correlating the results of Modified-Modified Schober Test with those of the kinovea software.

Intra-rater reliability of Kinovea Software Measurement

Time Frame: 1 year

To evaluate Intra-rater reliability, the 1st examiner will analyze the video that will be recorded at the 1st assessment and 1 week later using kinovea and the results will be compared.

Inter-rater reliability of Kinovea Software Measurement

Time Frame: 1 year

To evaluate Inter-rater reliability, 1st and 2nd examiner will analyze the video recorded in the 1st assessment using kinovea and the results will be compared.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dina Mohamed Ramadan

Principal investigator

Cairo University

Study Sites (1)

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