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NCT06187974Completed

Relationship of Proprioception, Reaction Time and the Gait and Balance Parameters After Stroke

Assessment of the Relationship Between the Deficit of Proprioception, Reaction Time and the Parameters of Gait and Balance in Stroke Patients

Source: ClinicalTrials.gov · Last updated 7 May 2026

Brief summary (registry, in English)

The aim of this observational study is to analyze how impaired proprioception affects the gait, reaction time, balance and functioning of stroke patients. Research questions: * Are there correlations between the deficit of proprioception and reaction time and the parameters of gait and balance as well as the functional state of stroke patients? * Are there relationships between factors such as proprioception, reaction time, balance, functional status and gait, and time since stroke, the hemisphere where the stroke occurred, and gender? * Are there differences in proprioception deficits and reaction times between the lower limbs in stroke survivors? Participants will be assessed once using standard functional clinical tests and the rehabilitation devices. Researchers will compare stroke patients and healthy volunteers to see, if there are differences in proprioception deficits, reaction time and balance.

Status (registry)
Completed
Study type
Observational
Enrollment
132 (actual)
First submitted
3 Jul 2023
Start date
8 Nov 2023
Primary completion date
31 Oct 2024
Lead sponsor
University of Rzeszow
Diseases
Stroke
NCT number
NCT06187974

What you commit to

  • Study type: Observational
  • Participants enrolled: 132
  • From 8 Nov 2023 to the primary completion date, 31 Oct 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • second or subsequent stroke,
  • stroke of the brainstem and cerebellum,
  • epilepsy,
  • disorders of higher mental functions,
  • coexisting neurological, rheumatological, orthopedic diseases,

Other

  • lack of informed and voluntary consent of the patient,
  • use of orthopedic supplies during locomotion.

Who the study is looking for

  • informed and voluntary consent of the patient,
  • first-time stroke,
  • hemiparesis,
  • time from stroke to 3 months,
  • age 30-75,
  • grade 3-5 in the Functional Ambulation Category,
  • walking without orthopedic support.

Age in the registry: 30 years to 75 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Rehabilitation, Clinical Regional Hospital number 2
Coordinator of this site? Confirm its status
RzeszówPolandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.