Effect of Neuroproprioceptive "Facilitation, Inhibition" Physical Therapy Using Virtual Reality on Upper Limb Mobility and Postural Stability in Multiple Sclerosis

CompletedNot a drug-phase studyMS (type not specified)NCT04807738

What it found

Paper found, not read

A paper reports the results; we have not read it yet. See Papers below.

What was tested

Treatment tested

  • Neuroproprioceptive "facilitation and inhibition" in virtual reality

Compared with

  • Neuroproprioceptive "facilitation and inhibition"

What it measured

Main measures

  • Nine Hole Peg Test (9HPT) - change pre/post intervention

    Pre-assessment (baseline testing), Post-assessment (immediately in a week following the last procedure)

    Disability progression
  • Box and Block Test (BNB) - change pre/post intervention

    Pre-assessment (baseline testing), Post-assessment (immediately in a week following the last procedure)

    Arm and hand function
  • Hand Grip Strength (HGS) -change pre/post intervention

    Pre-assessment (baseline testing), Post-assessment (immediately in a week following the last procedure)

    Arm and hand functionPhysical function
  • Tremor; Frequency for which the smoothed power spectral density is maximal (fMAX)

    Pre-assessment (baseline testing), Post-assessment (immediately in a week following the last procedure)

    Physical function
  • Tremor; Power of the signal in band from f1 to f2 (Pf1-f2)

    Pre-assessment (baseline testing), Post-assessment (immediately in a week following the last procedure)

    Physical function
  • Five times Sit to Stand test (5STS) -change pre/post intervention

    Pre-assessment (baseline testing), Post-assessment (immediately in a week following the last procedure)

Other measures (2)

  • Multiple Sclerosis Impact Scale (MSIS-29) - change pre/post intervention

    Pre-assessment (baseline testing), Post-assessment (immediately in a week following the last procedure)

    Quality of life (reported by participants)
  • EQ-5D-3L-health questionnaire - change pre/post intervention

    Pre-assessment (baseline testing), Post-assessment (immediately in a week following the last procedure)

    Walking and mobilityPainMood and sleepQuality of life (reported by participants)

Who could take part

MS (type not specified) · 18 to 75

Show the full criteria

Inclusion criteria

* The inclusion criteria comprise of a definite diagnosis of multiple sclerosis, EDSS score ≥ 2 a ≤ 7 ((10); determined by neurologist), no history of relapse, no history of change in disease-modifying treatment, no history of corticosteroid therapy in the past three months prior to recruitment.

Exclusion criteria

* The exclusion criteria include other factors influencing mobility (history of stroke, pregnancy, traumatic injury of limb/s. Severe cardiovascular or orthopedic dysfunction, impaired cognitive functions in the course of examination and/or consecutive therapy.

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

The randomized controlled trial is aimed to study the efficacy of virtual reality (VR) and its impact on upper limb function and postural stability in people with mild to severe multiple sclerosis (pwMS). The conceptual idea is to compare two kinds of neuroproprioceptive "facilitation and inhibition" physical therapy, first in a real environment and second in virtual reality, in out-patient therapy that will be held in 15 hourly therapies, 2x a week in a period of two months. The efficacy will be assessed by a blinded independent clinical examiner using clinical examination and questionnaire survey before and in a week following the therapeutic intervention. The main focus is on upper limb gross and fine motor skills, trunk stability and stability, and sit to stand stability.

Papers

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History

    1. Started

      Apr 2021

    2. Main results due

      Jan 2025

    3. Finished

      Feb 2025

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