Clinical Trial Details
— Status: Active, not recruiting
Administrative data
NCT number |
NCT05024240 |
Other study ID # |
ID 14827 |
Secondary ID |
|
Status |
Active, not recruiting |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
October 10, 2018 |
Est. completion date |
December 2021 |
Study information
Verified date |
August 2021 |
Source |
Charles University, Czech Republic |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial 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.
Description:
The aim of this research will be to describe the interaction between cognitive and cognitive
sensory tasks and stability in patients whose disease impairs the ability to maintain a
stable upright position, for example in patients with cerebellar syndromes. And further
compare this interaction with a control group of healthy probands. This interaction will be
investigated in variously demanding postural situations (eg. standing on both lower limbs,
with the exclusion of visual control, with reduced proprioceptive input from the patch).
Patient stability will be quantified using a stabilometric examination on the Kistler
platform (Kistler Instrumente AG, Switzerland). investigators will quantify the performance
of patients in secondary tasks using parameters such as response time to response and success
in assigned tests.
The expected number of probands is 20 individuals in both groups. Study will objectify
postural stability by means of a static stabilometric examination on the Kistler platform,
the recording length of each postural situation will be 30 s. Four different demands of
postural tasks were chosen - a bipedal stand, a bipedal stand with the exclusion of visual
control, a stand on a foam pad and a stand on a foam pad with the exclusion of visual
control. To evaluate postural deviations, investigators chose the following CoP parameters:
stabilogram curve length and stabilogram area. During the stabilometric measurement, the
number of touches of the guardrail will also be recorded, or the number of falls or touches
with a lightened limb of the pad or the other limb during the measurement. Testing will take
place in the Neurological Laboratory of the Department of Neurology, 2nd Faculty of Medicine,
Charles University in Prague and FN Motol.
Gradually, two types of secondary task will be added to the postural tasks, with visual input
(modified Stroop test) and a purely cognitive task (Backward counting test). At first,
probands will be acquainted with what types of tasks await them during the experiment and
will be able to train each of them in two trial experiments. This will be followed by testing
trials in random order (cognitive tests in single-task situations, namely sitting in a chair,
single task postural tasks and dual-task situations).