VR-based Dexterity Training in MS

NCT ID: NCT07193602

Last Updated: 2025-09-26

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

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-11-01

Study Completion Date

2027-11-01

Brief Summary

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The aim of the study is to investigate if a specifically developed home-based dexterity training intervention using a Virtual Reality (VR) Headset (Meta quest 2) improves impaired manual dexterity in persons with multiple sclerosis.

Detailed Description

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Conditions

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Multiple Sclerosis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Prospective, randomized-controlled, home-based, multi-center, rater-blinded parallel-arm pilot study.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors
Raters will not be involved in the screening and randomisation process and blinded with regard to the treatment group

Study Groups

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Experimental intervention = training intervention (Group1)

Eight training programs will be performed addressing different key movements of the hand/arm. All training programs will be performed in sitting position. Training will be performed for 4 weeks, 5 days/week. All 8 training programs will be performed on every training day which corresponds to approximately 20min training/day.

Group Type EXPERIMENTAL

VR-based dexterity training in MS

Intervention Type DEVICE

Training of limited manual dexterity in people with multiple sclerosis through a specially developed home-based dexterity training programm using a virtual headset

Control inervention = Sham-Intervention (Group2)

The Sham-Intervention will be the commercially available meditations App "TrippĀ®". During a period of four weeks, patients will perform the Sham intervention 3 times a week, each session being approximately 20 minutes.

Group Type SHAM_COMPARATOR

mediation program

Intervention Type OTHER

Sham Training is the comparator. The Sham group is performing a commercially available mediation programm TRIPP:

Interventions

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VR-based dexterity training in MS

Training of limited manual dexterity in people with multiple sclerosis through a specially developed home-based dexterity training programm using a virtual headset

Intervention Type DEVICE

mediation program

Sham Training is the comparator. The Sham group is performing a commercially available mediation programm TRIPP:

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* MS patients with relapsing-remitting MS (RRMS), secondary-progressive MS (SPMS) or primary progressive MS (PPMS) according to the revised McDonald's criteria (Thompson et al. 2017).

Age between 18 and 75 years.

Written informed consent signed by the subject must be obtained prior to study start

Patient must complain about MS related impaired manual dexterity negatively affecting ADL and/or QoL.

Patients must have a pathological 9-Hole-Peg-Test (9HPT) as defined by Oxford Grice et al. 2003.

Patients must have Arm function in multiple sclerosis questionnaire (AMSQ) score \>41

Exclusion Criteria

* A relapse that started within 60 days prior to screening.

Rapidly progressive disease.

Any disease/condition that impaired manual dexterity besides MS

Any disease other than MS that could possibly explain the patient's signs and symptoms

Medical or psychiatric conditions that compromise the ability to comply with the protocol, or to complete the study

A history of drug abuse in the 12 months prior to screening
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Basel, Switzerland

OTHER

Sponsor Role collaborator

Christian Kamm

OTHER

Sponsor Role lead

Responsible Party

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Christian Kamm

Prof. Dr. med.

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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MS Centre, Neurology, University hospital Basel

Basel, Basel, Switzerland

Site Status

Lucerne Cantonal Hospital

Lucerne, Canton of Lucerne, Switzerland

Site Status

Countries

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Switzerland

Central Contacts

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Christian Kamm, Prof. Dr. med.

Role: CONTACT

0041 41 205 29 69

Facility Contacts

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Marcus D'Souza, PD Dr. med.

Role: primary

0041 61 556 58 54

Christian Kamm, Prof. Dr. med

Role: primary

0041 41 205 29 69

References

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Other Identifiers

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LUKSKAMM003

Identifier Type: -

Identifier Source: org_study_id

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