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

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

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05609461
Enrollment
0
Registered
2022-11-08
Start date
2022-10-25
Completion date
2023-08-31
Last updated
2023-06-22

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

Conditions

Stroke

Keywords

Gait Analysis, Foot-Ankle Orthosis, Knee Hyperextension, Kinematic Analysis

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.

Interventions

None listed

Sponsors

Atılım University
CollaboratorOTHER
Hacettepe University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Kinematic AnalysisBaselineAt 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.

Countries

Turkey (Türkiye)

Outcome results

None listed

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