Viewing Study NCT05839977



Ignite Creation Date: 2024-05-06 @ 6:56 PM
Last Modification Date: 2024-10-26 @ 2:57 PM
Study NCT ID: NCT05839977
Status: RECRUITING
Last Update Posted: 2023-05-03
First Post: 2023-04-20

Brief Title: The Effect of Telerehabilitation on Balance in People With Multiple Sclerosis
Sponsor: Charles University Czech Republic
Organization: Charles University Czech Republic

Study Overview

Official Title: Possibilities of Using Telerehabilitation for the Therapy of Balance and Walking Disorders in Patients With Multiple Sclerosis in Clinical Practice
Status: RECRUITING
Status Verified Date: 2023-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The study will compare the effect of individual telerehabilitation with offline remote exercise through videos and with a control group without intervention The monitored group will be people with multiple sclerosis with balance impairment The duration of the intervention will be 12 weeks
Detailed Description: Total of 60 persons will be randomly divided into two experimental and one control groups After dividing into individual groups all probands will be examined using objective and subjective tests for balance and walking The same testing will be done after the end of the 12-week intervention

The group with individual telerehabilitation will exercise twice a week The exercise will consist of strength and balance exercises using the Homebalance system For direct synchronous contact between the physiotherapist and the patient an audiovisual link via the freely available ZOOM app was used

The second experimental group will receive 12 video recordings of exercises created by a physiotherapist for home exercises according to which they will also exercise twice a week

The control group receives no intervention

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None