The Effect of Neurorehabilitation Therapy on Postural Control, Mobility and Quality of Life in Multiple Sclerosis Patients

NCT ID: NCT03424538

Last Updated: 2020-04-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-02-05

Study Completion Date

2018-06-10

Brief Summary

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Abstract Introduction: Postural control disorders are the most common motor disorder associated with multiple sclerosis.

Objective: The aim of this study is to demonstrate the potential for improvement of postural control, motion performance and quality of life in patients with multiple sclerosis who are performing a special neurorevolutionary balancing program.

Intervention: The treated group (n = 15) performed five times a week for the treatment we defined. (60 minutes per day). The experimental group performed movements using the Xbox 360 and Kinect consoles. The study team participated in 25 sessions, five times a week. The duration of treatment was 5 weeks.The MStp group (n=14) participated in a 5-week physiotherapy course. The general treatment consisted of strengthening, stretching and walking correction. During the 5-week period, 25 patients attended training. One treatment takes 60 minutes. Sensory Organisation Test / Body Sway at the end of the baseline and treatment protocol is used to evaluate each patient. The quality of life mapping was measured by subjective tests (EQ-5D-5L, ADL). To assess the depressive state, a Beck depression questionnaire was used. Balance and motion performance were used by the Berg Balance Test and 6Minutes Walk Test. The results were compared with the control group results (n = 14) and showed improvement in overall balance and motion performance.

Detailed Description

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Conditions

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Multiple Sclerosis, Chronic Progressive Multiple Sclerosis, Primary Progressive

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The single-arm, 5-week intervention is monitor every day on the effect of postural control on walking performance, balance and quality of life. The intervention team (n = 15) takes 25 training sessions for 5 weeks. Every move takes 60 minutes to continuously increase the load intensity of the X-box program. Before each intervention started, the patients perform a 10 minute warm-up and the drainage exercises are 15 minutes stretching exercises. The MStp group (n=14) participated in a 5-week physiotherapy course. The general treatment consisted of strengthening, stretching and walking correction. During the 5-week period, 25 patients attended training. One treatment takes 60 minutes. The control group (n = 14) did not receive physiotherapeutic treatment outside the medication.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Investigators

Study Groups

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MSt

The MSt group that received 5 weeks of intensive therapy.

Group Type EXPERIMENTAL

Neurorehabilitation

Intervention Type OTHER

5-week-long intervention, administered daily, targeted postural instability, balance and mobility using at-limit intensity sensorimotor and visuomotor agility training

MSc

The MS controll group that did not receive treatment.

Group Type NO_INTERVENTION

No interventions assigned to this group

MStp

The MStp Group performs a traditional physiotherapy for 5 weeks.

Group Type EXPERIMENTAL

Physiotherapy

Intervention Type OTHER

5-week-long intervention, physiotherapy, stretching, walking preparation, strengthening

Interventions

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Neurorehabilitation

5-week-long intervention, administered daily, targeted postural instability, balance and mobility using at-limit intensity sensorimotor and visuomotor agility training

Intervention Type OTHER

Physiotherapy

5-week-long intervention, physiotherapy, stretching, walking preparation, strengthening

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Multiple Sclerosis
* instability problem

Exclusion Criteria

* Severe heart problems, severe demeanor, alcoholism, drug problems
Minimum Eligible Age

35 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Medical Center Groningen

OTHER

Sponsor Role collaborator

Somogy Megyei Kaposi Mór Teaching Hospital

OTHER

Sponsor Role lead

Responsible Party

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Tollár József

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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József Tollár, MSC

Role: PRINCIPAL_INVESTIGATOR

Somogy Megyei Kaposi Mór Teaching Hospital

Locations

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Somogy Megyei Kaposi Mór Teaching Hospital

Kaposvár, Somogy County, Hungary

Site Status

Countries

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Hungary

Related Links

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Other Identifiers

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IKEB008/2017

Identifier Type: -

Identifier Source: org_study_id

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