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Interaction of the Cognitive and Sensory-cognitive Tasks With Postural Stability in Individuals With Stability Disorders

NCT05024240 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2021-08-27

No results posted yet for this study

Summary

The aim of this study is to describe the interaction of the cognitive and visual-cognitive task with postural stability in patients suffering by cerebellar ataxia. Investigators will measure changes in postural stability parameters and in secondary task performance, which should show the ability of the patients to manage the dualtask situations.

Conditions

  • Cerebellar Ataxia
  • Cerebellar Diseases

Interventions

DIAGNOSTIC_TEST

Stabilometry

Probands will stand on stabilometric platform (double leg stance) and we will measure CoP parameters area and length. We also make this task harder by using foam and exclusion of visual control. Length of one test is 30s.

DIAGNOSTIC_TEST

Stroop test

There are various names of colours written in non-matching font colour in this test. During this test probands are required to name the colour which is written in text not the colour of the font. We will measure reaction time and number of mistakes.

DIAGNOSTIC_TEST

Backward counting test

In this counting test probands are given number from interval \<180-200\> and they are asked to subtract 7 during 30s interval of the testing. We will measure reaction time and number of mistakes.

Sponsors & Collaborators

  • Charles University, Czech Republic

    lead OTHER

Principal Investigators

  • Pavel Kolář, Prof. PaedDr. Ph.D. · Department of Rehabilitation and Sports Medicine, Second Faculty of Medicine, Charles University

  • Ondřej Čakrt, Doc. PhDr. Ph.D. · Department of Rehabilitation and Sports Medicine, Second Faculty of Medicine, Charles University

  • Kateřina Levínská, Mgr. · Department of Rehabilitation and Sports Medicine, Second Faculty of Medicine, Charles University

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-10-10
Primary Completion
2021-09-30
Completion
2021-12-31

Countries

  • Czechia

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05024240 on ClinicalTrials.gov