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NCT05885282Completed

Investigation of the Effects of Local Vibration Applied to Different Regions and Spinal Stabilization Exercises

Investigation of the Effects of Local Vibration Applied to Different Regions and Spinal Stabilization Exercises on Postural Control in Patients with Ataxic Multiple Sclerosis

Source: ClinicalTrials.gov · Last updated 2 Oct 2024

Brief summary (registry, in English)

The aim of this study is to investigate the effects of local vibration application applied to different regions on postural control in addition to spinal stabilization training in ataxic multiple sclerosis (MS) patients. The study was planned as a single-blind, randomized controlled trial. The patients included in the study will be divided into 3 groups by the closed-envelope randomization method. Each treatment will be 8 weeks, 3 days a week. The control group will be given 40 minutes of lumbar spinal stabilization exercises. Paraspinal vibration group; In addition to 40 minutes of lumbar spinal stabilization exercises, LV will be applied to the paraspinal muscles for 10 minutes. LV application will be applied to the cervical paraspinal muscles for 5 minutes and to the lumbar paraspinal muscles for 5 minutes, bilaterally, sequentially. Gastrosoleus vibration group; In addition to 40 minutes of lumbar spinal stabilization exercises, LV will be applied to the gastrosoleus muscle complex for 10 minutes. LV application will be applied bilaterally, sequentially (5 minutes on the right and left). Assessments will be made by a blind assessor. In assessments; demographic information, Expanded Disability Status Scale (EDSS) /Extended Disability Status Scale (disease stage), International Cooperative Ataxia Rating Scale (ataxia severity), Berg Balance Scale (performance-based balance), Trunk Impairment Scale (trunk control), Neurocom Balance Master Static Posturography (limits of stability and postural sway), OptoGait (gait analysis), lumbopelvic muscle endurance tests will be used.

Status (registry)
Completed
Study type
Interventional
Enrollment
30 (actual)
First submitted
10 May 2023
Start date
27 Jul 2023
Primary completion date
1 Jun 2024
Lead sponsor
Hacettepe University
NCT number
NCT05885282

What you commit to

  • Study type: Interventional
  • Participants enrolled: 30
  • From 27 Jul 2023 to the primary completion date, 1 Jun 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

  • Having a history of attacks in the last 3 months

Other

  • Having orthopedic or systemic problems
  • Presence of peripheral vestibular complaints
  • Participating in another exercise program in the last 6 months
  • Being mentally affected (Mini-Mental Test Score \< 24)
  • Severe spasticity (MAS\>3)
  • Refusal to participate in the study

Who the study is looking for

  • Being between the ages of 18-50
  • Having been diagnosed with MS by a neurologist
  • EDSS score between 3-5
  • EDSS pyramidal system score of 3 or less
  • Not using corticosteroids and/or stopping at least 3 months before starting the study

Age in the registry: 18 years to 50 years · Sex: All · Does not accept 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
Hacettepe University Faculty of Health Sciences Department of Physical Therapy and Rehabilitation
Coordinator of this site? Confirm its status
AnkaraTurkey (Türkiye)Unknown status

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