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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04672057
Enrollment
108
Registered
2020-12-17
Start date
2017-07-08
Completion date
2018-06-21
Last updated
2020-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemiparesis

Keywords

Hemiparesis, Lateralization, Spatio-temporal analysis, Gait

Brief summary

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

Detailed 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.

Interventions

OTHERassessment 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.

Sponsors

Pamukkale University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frameDescription
assessment of gait between in right and left hemipareticsMeasurement time is 10 minutes. Only one measurement was made.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.

Secondary

MeasureTime frameDescription
assessment of gait between in hemiparetic and healthy individualsMeasurement time is 10 minutes. Only one measurement was made.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.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026