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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 26 October 2021
Main ID:  NCT03637023
Date of registration: 10/08/2018
Prospective Registration: Yes
Primary sponsor: Farzin Hajebrahimi, PT, MSc
Public title: Virtual Reality for Parkinson's Disease
Scientific title: Clinical and Rest-fMRI Effects of Virtual Reality Practice on Motor and Cognitive Symptoms in Parkinson's Disease, a Randomized Control Trial
Date of first enrolment: August 18, 2018
Target sample size: 30
Recruitment status: Terminated
URL:  https://clinicaltrials.gov/show/NCT03637023
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Participant, Investigator).  
Phase:  N/A
Countries of recruitment
Turkey
Contacts
Name:     Farzin Hajebrahimi
Address: 
Telephone:
Email:
Affiliation:  Medipol University
Name:     Lutfu Hanoglu, Professor
Address: 
Telephone:
Email:
Affiliation:  Medipol University
Key inclusion & exclusion criteria

Inclusion Criteria:

- To be 50 years old and older

- Clinical diagnosis of PD within the -framework of Brain Bank criteria

- Getting a stable antiparkinsonian medication at least for the last 1 month (or the
treatment has not changed)

Exclusion Criteria:

- Having a story of unstable medical condition

- History of head trauma, stroke, or exposure to toxic substances

- Implying Parkinson plus syndromes in neurological examinations; pyramidal, cerebellar
examination findings, gaze paresis, autonomic dysfunction

- Being diagnosed with Dementia



Age minimum: 50 Years
Age maximum: 85 Years
Gender: All
Health Condition(s) or Problem(s) studied
Virtual Reality Therapy
Functional Magnetic Resonance Imaging
Parkinson Disease
Intervention(s)
Behavioral: Exercise Therapy
Behavioral: Virtual Reality
Primary Outcome(s)
Motor Level [Time Frame: Change from Baseline at 4 weeks.]
Cognitive Level [Time Frame: Change from Baseline at 4 weeks.]
Neuroplasticity [Time Frame: Change from Baseline at 4 weeks.]
Secondary Outcome(s)
Balance Confidence [Time Frame: Change from Baseline at 4 weeks.]
Balance [Time Frame: Change from Baseline at 4 weeks.]
Cognitive Assessment [Time Frame: Change from Baseline at 4 weeks.]
Quality of Life in patients with Parkinson's Disease [Time Frame: Change from Baseline at 4 weeks.]
Depression [Time Frame: Change from Baseline at 4 weeks.]
Mobility [Time Frame: Change from Baseline at 4 weeks.]
Functional Capacity [Time Frame: Change from Baseline at 4 weeks.]
Secondary ID(s)
PD-VR-2018
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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