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RecruitingNCT05965661Updated Jul 28, 2023

A New 3D Virtual Reality-based Upper Limb Training to Improve Dexterity in Parkinson's Disease

An interventional study of virtual reality upper limb hand training and virtual reality control training in Parkinson Disease, sponsored by Luzerner Kantonsspital. Recruiting at 1 site in Switzerland. Open to participants aged 40 Years to 99 Years. Per ClinicalTrials.gov, last updated 2023-07-28.

Sponsored by Luzerner Kantonsspital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 9 months ago, but the record still lists the study as recruiting.
  • Started Jul 2023; still recruiting 3 years 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Randomized
Ages
40 Years to 99 Years
Sex
All
01

Study summary

We investigate the impact of a 4-week virtual reality-based upper limb training in Parkinson's disease. The benefits on dexterity of this training program will be evaluated.

For these purposes, a randomised, two arm, single assessor blind, parallel design with a monocentric, study setup will be performed.

Read the detailed description

Patients with Parkinson's disease (PD) suffer from significantly decreased coordination and have difficulties with precise hand/finger movements during the performance of both basic activities of daily living (ADL), such as dressing, grooming as well as higher ADL, such as cooking, shopping and regular medication intake. These difficulties further add to the burden of the disease, leading to reduced quality of life (QoL). A relatively new, but rapidly growing aspect of training in PD neurorehabilitation offers virtual reality (VR). We explore the effects of a VR-based upper limb hand training compared to a VR control training, which is less specific for dexterity. Moreover, we examine the effetcs of the trainings on upper limb related ADL, and therefore the impact on QoL in patients with PD.

02

Conditions studied

  • Parkinson Disease

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Keywords

  • Parkinson Disease
  • virtual reality training
  • dexterity
  • Parkinsonian Disorders
  • Basal Ganglia Diseases
  • Brain Diseases
  • Central Nervous System Diseases
  • Nervous System Diseases
  • Movement Disorders
  • Neurodegenerative Diseases
03

In context

Parkinson Disease

4,487 studies on the registry are indexed under Parkinson Disease; 1,082 are open to participants now.

This study's planned enrollment of 20 is below the median of 40 across 3,294 interventional studies indexed under Parkinson Disease.

Browse Parkinson Disease studies →

Lead sponsor

Luzerner Kantonsspital is the lead sponsor of 60 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients with confirmed PD, according to UK Brain bank Criteria
  • Hoehn \& Yahr Stadium I to IV
  • Age 40 to 99 years
  • written and signed informed consent
  • self-reported dexterous difficulties

Exclusion criteria

Exclusion Criteria:

  • MoCA \<21/30
  • psychiatric disease
  • participation on other interventional trials
  • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc.
  • severe visual impairment
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
20 participants (estimated)

Study arms

  • Other
    Virtual reality upper limb hand training

    The PD patients randomized in the experimental group will receive virtual reality upper limb hand training.

    Other: virtual reality upper limb hand training

  • Other
    Virtual reality control training

    The PD patients randomized in the control group will receive virtual reality control training.

    Other: virtual reality control training

Interventions

  • Othervirtual reality upper limb hand training

    The PD patients randomized in the experimental group will receive virtual reality upper limb hand training.

  • Othervirtual reality control training

    The PD patients randomized in the control group will receive virtual reality control training.

06

What researchers measure

Primary outcomes

  1. fine finger movements

    Coin rotation task (CRT): The CRT measures fine coordinated finger movements and is a suitable and valid dexterity test in patients with PD. The seconds for 20 halfturns will be measured.

    Time frame: 4 weeks

Secondary outcomes

  1. hand dexterity

    Nine Hole Peg test (9-HPT): The 9-HPT is a standardized, well established, and reliable measure of hand dexterity in patients with PD. seconds will be measured.

    Time frame: 4 weeks

  2. grip strenght

    The handheld JAMAR dynamometer measures the grip strength. kg will be measured.

    Time frame: 4 weeks

  3. motor function

    MDS-Sponsored Revision of the Unified Parkinson Disease Rating Scale (MDS-UPDRS III): It evaluates motor aspects of Parkinson's disease

    Time frame: 4 weeks

  4. self-reported dexterity related problems in daily living

    Dexterity Questionnaire 24 (DextQ-24): This questionnaire is a standardized patient self-rated outcome measure (PROM) for evaluating dexterity related ADL in PD. score range 24-96, higher scores mean more dexterity problems.

    Time frame: 4 weeks

  5. self-reported problems in quality of life

    Parkinson's Disease Questionnaire (PDQ-39): This questionnaire is a standardized patient self-rated outcome measure (PROM) for evaluating QOL in PD. range 0-156, higher values mean more problems.

    Time frame: 4 weeks

07

Study locations

1 of 1 sites recruiting
  • Luzerner Kantonsspital
    Lucerne, 6000, Switzerland
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 28, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05965661
Lead sponsor
Luzerner Kantonsspital
Responsible party
Sponsor
First posted
Jul 28, 2023
Start date
Jul 19, 2023
Primary completion
Dec 31, 2025 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Jul 28, 2023

Study contacts

Cornelia Cox, MSc
Contact
cornelia.cox@luks.ch
041 205 56 80
Manuela Pastore, PhD
Contact
manuela.pastore@luks.ch
041 205 72 20
Tim Vanbellingen, Prof
principal investigator · Luzerner Kantonsspital

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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