Investigation of the Spatio-temporal Gait Parameters in Individuals With Hemiparesis: Effect of Lateralization

Hemiparesis Clinical Trial

Official title:

Investigation of the Spatio-temporal Gait Parameters in Individuals With Hemiparesis: Effect of Lateralization

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04672057
• Other study ID #: Gait Parameter In Hemiparetics
• Status: Completed
• Phase: N/A
• Start date: July 8, 2017
• Est. completion date: June 21, 2018

Study information

• Verified date: December 2020
• Source: Pamukkale University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The aim of this study was to investigate the effect of lateralization on the spatio-temporal characteristics of gait in individuals with hemiparesis.

Description:

A total of 108 individuals within the age range of 20-65 and 36 of whom are right hemiparetic (Group1; 16F, 20M), 36 of whom are left hemiparetic (Group2; 16F, 20M) and 36 of whom are healthy (Group3; 19F, 17M) have been included in the study. BTS G-Walk Gait Analysis System has been used to assess the spatio-temporal gait characteristics.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 108
• Est. completion date: June 21, 2018
• Est. primary completion date: May 8, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 65 Years

Eligibility

Inclusion Criteria:

for the hemiparetic individuals

• Being between the ages of 20-65,

• Having a stroke for the first time and one-sidedly,

• Having a stable clinical state,

• Having no cognitive disorder (Hodkinson Mental Test = 8),

• Having = 3 from Modified Rankin Score,

• Having no problems with vision and hearing.

for the healthy control group;

• Being between the ages of 20-65

• Having no neurological, musculosceletal, cardiac and cognitive problems that was undergone before and may affect walking.

Exclusion Criteria:

• The existence of vision and hearing problems in both study and control groups,

• The existence of orthopedic, neurological and psychiatric problems that may affect walking.

Related Conditions & MeSH terms

• Hemiparesis
• Paresis

Intervention

Other:
• assessment of gait parameters
Gait parameters have been recourded with the use of BTS G-Walk Wireless Digital Walking Analysis System on a 10-meter smooth walking area.

Locations

Country	Name	City	State
Turkey	Pamukkale University	Denizli

Sponsors (1)

Lead Sponsor	Collaborator
Pamukkale University

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	assessment of gait between in right and left hemiparetics	A port was attached to the patient's L5-S1 level. In the gait analysis system, the results was transferred to the computer via bluetooth with the analysis port. The resulting report was generated automatically. The report measured gait speed, cadence, right and left step length, right and left stride length, double and single stride length, pelvic rotation, pelvic tilt, and pelvic oblique.	Measurement time is 10 minutes. Only one measurement was made.
Secondary	assessment of gait between in hemiparetic and healthy individuals	A port was attached to the patient's L5-S1 level. In the gait analysis system, the results was transferred to the computer via bluetooth with the analysis port. The resulting report was generated automatically. The report measured gait speed, cadence, right and left step length, right and left stride length, double and single stride length, pelvic rotation, pelvic tilt, and pelvic oblique.	Measurement time is 10 minutes. Only one measurement was made.