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Enrolling by Invitation

NCT Number: NCT06448065

Gait Classification in Children With Cerebral Palsy, a Reliability Study

The goal of this observational study is to assess whether gait classification patterns can be reliably obtained from video recordings in comparison with three-dimensional kinematic data.

The main questions it aims to answer are:

Are gait classifications from video recordings reliable between raters? Are gait classifications from video recordings valid in comparison with three-dimensional kinematic data?

Gait analysis data from participants who visited the gait lab in the Karolinska Hospital will be used for this purpose.

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Key information

Age range

3 year–18 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Karolinska University Hospital

Stockholm, 17176, Sweden

About this study

Current retrospective observational study aims to assess the reliability and validity of gait pattern classification systems in ambulatory children with CP. Gait classification is often performed using kinematic gait data obtained via a three dimensional (3D) data captured in a specialized gait lab using infra-red cameras. However, not all hospitals and clinical centers have access to such a specialized gait lab, and therefore often use video recordings as an alternative for gait classification. It is currently not known whether such a classification based on solely video recordings is equally reliable in comparison with kinematic gait data. For this purpose, current study aims to assess the reliability and validity of video recordings to classify children with CP according to predefined gait classifications. Sagittal plane video recordings during barefoot walking in children with CP will be used to classify the study participants into seven different gait classification patterns. For reliability, inter-rater reliability between raters scoring the video recordings will be assessed. To evaluate whether video recordings could serve as a valid alternative for kinematic gait data, the agreement between the classifications from the video recordings and the kinematic data additionally will be assessed.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Main diagnosis of spastic cerebral palsy
  • Age 3 to 18 at the time of gait analysis
  • Availability of barefoot walking data collected at the Karolinska Hospital gait lab
  • Written informed consent of both parents to use the clinically collected data as research data

Exclusion criteria

  • Main diagnosis of dyskinetic or ataxic cerebral palsy
  • No barefoot walking trials available
  • No kinematic data available
  • BTX-A injections 6 months prior to gait analysis
  • Orthopaedic surgery one year prior to gait analysis

Treatment and study plan

Primary outcomes

  1. Inter-rater reliability

    Time frame: approximately 12 months

    Assess inter-rater reliability between multiple raters assessing video recordings of gait in children with cerebral palsy

  2. Concurrent validity

    Time frame: approximately 12 months

    Assess concurrent validity between outcome classifications from video recordings and from three-dimensional gait kinematics children with cerebral palsy

Sponsors and collaborators

Lead sponsor

Region Stockholm

Other Gov

Collaborators

  • Karolinska Institutet
  • Karolinska University Hospital

Registry information

Official study title

A Reliability Study of Gait Classification in Children With Cerebral Palsy

Acronym: GCP

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Jun 7, 2024
Registry last updated
Jun 7, 2024

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.

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