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Clinical Trials/NCT05609461
NCT05609461
Withdrawn
N/A

Investigation of the Effect of Orthosis Use for Control of Knee Hyperextension in Chronic Stroke Patients by Kinematic Analysis

Hacettepe University1 site in 1 countryOctober 25, 2022
ConditionsStroke

Overview

Phase
N/A
Intervention
Not specified
Conditions
Stroke
Sponsor
Hacettepe University
Locations
1
Primary Endpoint
Kinematic Analysis
Status
Withdrawn
Last Updated
2 years ago

Overview

Brief Summary

The aim of this study is to examine the effect of using foot-ankle orthosis at different angles on hyperextension control in stroke patients.

The hypotheses of the study are:

Hypothesis 1:

Ho: The foot-ankle orthosis, which fixes the ankle at different angles (3 degrees of dorsiflexion - 5 degrees of dorsiflexion) in stroke patients, has no effect on the control of knee hyperextension.

H1: Foot-ankle orthosis, which fixes the ankle at different angles (3 degrees of dorsiflexion - 5 degrees of dorsiflexion) in stroke patients, has an effect on the control of knee hyperextension.

Registry
clinicaltrials.gov
Start Date
October 25, 2022
End Date
August 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Suleyman Korkusuz

Principal Investigator

Hacettepe University

Eligibility Criteria

Inclusion Criteria

  • Between the ages of 40 and 65
  • Six months must have passed since the stroke.
  • Ambulation regardless of the use of a walking aid (walker, cane, or tripod)
  • Obtaining between 0 and 3 Modified Rankin Score points
  • A score of 24 or higher on the Mini Mental Test is required to pass.
  • Hyperextension during the stance phase of gait.
  • Participating voluntarily in the study

Exclusion Criteria

  • Having a history of more than one stroke
  • Dementia is known to exist
  • Having a diagnosed orthopedic, mental, or neurological condition
  • Having a circumstance that impedes communication
  • Having a history of lower extremity and gait-related surgeries

Outcomes

Primary Outcomes

Kinematic Analysis

Time Frame: Baseline

At the specified anatomical sites of the participants, reflective signs will be placed. The participants will be required to walk 5 meters. The three-dimensional positions of these reflective marks will be captured by the 8-camera Vicon motion capture system. Using the blade software, it will be moved to the computer environment and kinematic data will be collected.

Study Sites (1)

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