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NCT Number: NCT07557186

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

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

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Key information

Age range

18 year–25 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Dina Mohamed Ramadan

Gamasa, Egypt

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.
  • Colon.
  • Subject takes any muscle relaxant.

Treatment and study plan

Primary outcomes

  1. 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.

  2. 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.

  3. 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Dina Ramadan, Master

CONTACT

[email protected]

01022302634

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Collaborators

  • Delta University for Science and Technology

Registry information

Official study title

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

Important dates

Study start
2027
Primary completion
2029
Study completion
2029
First posted
Apr 29, 2026
Registry last updated
Apr 29, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.