Skip to content

Functional Exercise in Virtual Environment for Persons With Multiple Sclerosis or Parkinson's Disease

Motivation, Neuropsychological Testing and Functional Exercise in Virtual Environment for Persons With Multiple Sclerosis or Parkinson's Disease

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04266444
Acronym
MEFA
Enrollment
108
Registered
2020-02-12
Start date
2020-02-06
Completion date
2021-09-29
Last updated
2021-09-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Multiple Sclerosis, Parkinson Disease

Keywords

exergaming, virtual reality, neuropsychological tests, motivation

Brief summary

The aim of the study is to optimise the hand dexterity exercising program in virtual reality (VR) for patients with multiple sclerosis and Parkinson's disease. Little research has been published on this topic, but the preliminary results are promising. Different levels of difficulty of a VR game will be tested. The patients will be assessed using neuropsychological tests of executive functions, visuospatial abilities, mental speed, flexibility and motor speed. Functional ability, coordination and cognitive abilities will also be assessed.

Detailed description

Each patient meeting the inclusion criteria will be randomised to one of the four groups (i.e., 10cubes game difficulty level). The patients will perform five exergaming sessions, each session lasting for 1 hour, on five consecutive working days within the period of two weeks. The 10cubes task requires that all 10 cubes are moved within 2 minutes. Each patient will perform the task 5 times in succession with 1-2 minute breaks. The patients will be assessed using the Box & Blocks Test, Frontal Assessment Battery (FAB), Delis-Kaplan Executive Function System (D-KEFS) and Judgment of Line Orientation (JLO) before the first session and after the last session. In addition, the patients will fill in the Intrinsic Motivation Inventory (IMI) after each session. Based on statistical sample size calculations, the study plan is to include 80 patients with Parkinson's disease and 12 patients with multiple sclerosis randomising them separately, so that the groups will be balanced in terms of size and diagnosis.

Interventions

The 10Cubes game (by I. Cikajlo) will be used. In the game, the motion of the hand, wrist and fingers is tracked by an infra-red camera (by LeapMotion, Inc.) and hand motion is reflected in the virtual environment. The software will run on a powerful computer with a 19 display. Each group will have the game set to a different level of difficulty.

Sponsors

University Rehabilitation Institute, Republic of Slovenia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* diagnose of Parkinson's disease or multiple sclerosis; * Mini Mental State Examination score above 24; * preserved upper limb function; * for Parkinson's disease patients Hoehn and Yahr scale score between 2 and 3.

Exclusion criteria

* any communicable disease; * severe vision impairment.

Design outcomes

Primary

MeasureTime frameDescription
Change in Box & Blocks Test from baselineAssessment at baseline and after two weeksStandard clinical test to assesses unilateral gross manual dexterity; the minimum possible score is 0, the maximum is 150; higher score indicates better outcome.
Change in Frontal Assessment Battery (FAB) score from baselineAssessment at baseline and after two weeksBrief neuropsychological test battery to assess executive functions; the minimum possible score is 0, the maximum is 18; higher score indicates better outcome.
Intrinsic Motivation Inventory (IMI) scoresAssessment at the end of each exergaming session; median across assessments will be taken as the outcome on each subscaleThe IMI is a multidimensional measurement instrument for assessing subjective experience of a target activity. The 22-item version that consists of four subscales will be used (scores range from 7 to 49 for one scale and from 5 to 35 for three scales); higher scores indicate better outcome.

Secondary

MeasureTime frameDescription
Change in Delis-Kaplan Executive Function System (D-KEFS) scores from baselineAssessment at baseline and after two weeksSet of nine subtests of executive functions with complex computerised scoring; higher scores indicate better outcome.
Change in Judgment of Line Orientation (JLO)Assessment at baseline and after two weeksStandardized test of visuospatial skills; the minimum possible score is 0, the maximum is 30; higher score indicates better outcome.

Countries

Slovenia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026