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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05965661
Other study ID # 2022-01545
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 19, 2023
Est. completion date December 31, 2025

Study information

Verified date July 2023
Source Luzerner Kantonsspital
Contact Cornelia Cox, MSc
Phone 041 205 56 80
Email cornelia.cox@luks.ch
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 31, 2025
Est. primary completion date December 31, 2025
Accepts healthy volunteers No
Gender All
Age group 40 Years to 99 Years
Eligibility 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: - 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

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Switzerland Luzerner Kantonsspital Lucerne

Sponsors (1)

Lead Sponsor Collaborator
Luzerner Kantonsspital

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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. 4 weeks
Secondary 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. 4 weeks
Secondary grip strenght The handheld JAMAR dynamometer measures the grip strength. kg will be measured. 4 weeks
Secondary motor function MDS-Sponsored Revision of the Unified Parkinson Disease Rating Scale (MDS-UPDRS III): It evaluates motor aspects of Parkinson's disease 4 weeks
Secondary 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. 4 weeks
Secondary 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. 4 weeks
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