Lower Extremity Proprioception Sensory and Functionality in Hemiparetic

February 20, 2025 updated by: Seref Duhan Altug, Istanbul Aydın University

Lower Extremity in Hemiparetic Proprioception Sensory and Functionality: A Comparative Study

The loss of sensorial feedback causes gait impairment in hemiparesis. The studies show that proprioceptive impairment of knee is related to falling in these patients. The aim of this study is to investigate the effects of proprioception on balance and gait functions in hemiparetic individuals.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Turkey
      • Istanbul, Turkey
        • Istanbul Aydın University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

Hemiparetic individuals Healthy individuals

Description

Inclusion Criteria:

  • Between the ages of 20-65 and discharged from the hospital,
  • Diagnosed with hemiparesis at least 4 weeks ago,
  • First time and unilateral hemiparesis,
  • Modified Rankin Score ≤ 3,
  • Hodkinson Mental Test ≥ 6,
  • Individuals who agree to receive treatment will be included in the study.

Exclusion Criteria:

  • Having vision and hearing problems,
  • Having other accompanying neurological, psychiatric and/or orthopedic problems other than hemiparesis,
  • Medically unstable,
  • Diseases that will affect the lower extremity sense,
  • Individuals with open wounds, circulation problems, and skin lesions in the area to be treated will be excluded from the study.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Proprioseption in hemiparetics
Proprioception on balance and gait functions in hemiparetic individuals
Other: Proprioseption in hemiparetics
Proprioception on balance and gait functions in hemiparetic individuals
Healthy Individual
Proprioception on balance and gait functions in healthy individuals
Other: Proprioseption in hemiparetics
Proprioception on balance and gait functions in hemiparetic individuals

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Sensorial Assessment-1
Time Frame: 2 minutes
Semmes-Weinstein Monoflament
2 minutes
Sensorial Assessment-2
Time Frame: 2 minutes
Position test for lower extremity
2 minutes
Sensorial Assessment-3
Time Frame: 2 minutes
Kinestesia (Electrogoniometer)
2 minutes
Balance assessment
Time Frame: 30 second
Static balance via SportKAT-550
30 second
Gait parameters
Time Frame: 1 minute
BTS G-Walk Spatiotemporal gait parameters
1 minute

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Istanbul Aydın University

Collaborators

Pamukkale University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2021

Primary Completion (Actual)

June 13, 2022

Study Completion (Actual)

July 13, 2022

Study Registration Dates

First Submitted

September 21, 2021

First Submitted That Met QC Criteria

September 21, 2021

First Posted (Actual)

September 30, 2021

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 20, 2025

Last Verified

February 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • E-60116787-020-78427

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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