Comparison of Walking Parameters Between Idiopathic Toe Walking and Independent Walking Diparetic Cerebral Palsy

Sponsor
Biruni University (Other)
Overall Status
Completed
CT.gov ID
NCT06142721
Collaborator
(none)
51
1
4
12.7

Study Details

Study Description

Brief Summary

The aim of the observational study is to compare static, kinematic and kinetic parameters with normal gait parameters in cases with Idiopathic toe walking (ITW) and Diparetic Cerebral Palsy (DCP) who have Gross Motor Function Classification System 1 level with the 3D Gait Analysis method, and to enable the early diagnosis of DCP and ITW. Male and female cases aged between 3-18 years will be included. This study will be carried out at Acıbadem Altunizade Hospital.

Condition or Disease Intervention/Treatment Phase
  • Other: 3D Gait Analysis

Detailed Description

It is an observational study. The aim of the observational study is to compare static, kinematic and kinetic parameters with normal gait parameters in cases with Idiopathic toe walking (ITW) and Diparetic Cerebral Palsy (DCP) who have Gross Motor Function Classification System 1 level with the 3D Gait Analysis method, and to enable the early diagnosis of DCP and ITW. Male and female cases aged between 3-18 years will be included. This study will be carried out at Acıbadem Altunizade Hospital. 51 cases will be included in our study. These cases will be divided into three groups. The first group will consist of patients diagnosed with idioaptic toe walking (n:17), the second group will be composed of diparetic cerebral palsy (n:15) with independent ambulation, and the third group will be the control group (n:19). First, the demographic information of the cases will be recorded. With 3D walking analysis, kinetic, kinematic and static data will be collected. The analysis of the obtained data will be done with Polygon Software (Vicon, Oxford, UK). Evaluated kinetic, kinematic and static parameters will be compared between three groups.

Is the lower extremity compensation of children with diparetic cerebral palsy who can walk independently more than children with idiopathic toe walking?

Study Design

Study Type:
Observational
Actual Enrollment :
51 participants
Observational Model:
Case-Control
Time Perspective:
Cross-Sectional
Official Title:
Comparison of Walking Parameters Between Idiopathic Toe Walking Children and Children With Independent Walking Diparetic Cerebral Palsy
Actual Study Start Date :
Sep 15, 2022
Actual Primary Completion Date :
Jan 15, 2023
Actual Study Completion Date :
Jan 15, 2023

Arms and Interventions

Arm Intervention/Treatment
ITW Group

3D gait analysis was applied to children with idiopathic toe walking. Static, kinematic and kinetic walking parameters were evaluated.

Other: 3D Gait Analysis
3D gait analysis was applied to children. Static, kinematic and kinetic walking parameters were evaluated

DCP Group

3D gait analysis was applied to diparetic children who were able to walk independently. Static, kinematic and kinetic walking parameters were evaluated.

Other: 3D Gait Analysis
3D gait analysis was applied to children. Static, kinematic and kinetic walking parameters were evaluated

Healthy Group

3D gait analysis was applied to healthy children. Static, kinematic and kinetic walking parameters were evaluated.

Other: 3D Gait Analysis
3D gait analysis was applied to children. Static, kinematic and kinetic walking parameters were evaluated

Outcome Measures

Primary Outcome Measures

  1. 3D Gait Analysis [Baseline]

    Sixteen markers defined according to the Modified Helen Heyes protocol are applied to certain anatomical regions of both lower extremities. 3D gait analysis can precisely calculate joint angles and movement patterns in all three planes. Collect spatio-temporal data.

Eligibility Criteria

Criteria

Ages Eligible for Study:
3 Years to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Voluntary consent from family

  • Diagnosed with idiopathic toe walking and spastic diparesis between the ages of 3-18.

  • Cases with GMFCS 1

  • The patients who applied to the healthy children's clinic, showed typical development, did not have any musculoskeletal and neurological problems, and wished to voluntarily participate in the study were included in the control group.

Exclusion Criteria:
  • Refusing to participate in the study

  • Under the age of 3 and over the age of 18

  • Not at GMFCS 1 level

  • Cases who did not have any orthopedic problems other than accompanying toe walking were excluded from the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Acıbadem Altunizade Hospital Istanbul Turkey

Sponsors and Collaborators

  • Biruni University

Investigators

  • Principal Investigator: Fatih Erol, Biruni University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fatih EROL, Principal Investigator, Biruni University
ClinicalTrials.gov Identifier:
NCT06142721
Other Study ID Numbers:
  • FEROL
First Posted:
Nov 21, 2023
Last Update Posted:
Nov 21, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Fatih EROL, Principal Investigator, Biruni University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 21, 2023