A Study of Neurofeedback for the Treatment of Parkinson's Disease

Not Applicable

• Conditions: Parkinson Disease
• Interventions: Other: Training with Neurofeedback; Other: The other Training with Neurofeedback

• Registration Number: NCT03837548
• Lead Sponsor: Osaka University

Brief Summary

This study aims to reveal relationship between brain activities and the symptoms of Parkinson disease when a neurofeedback training was applied for them.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2019-01-15
• Study First Submitted QC: 2019-02-09
• Study First Posted: 2019-02-12
• Study Start: 2019-06-01
• Status Verified: 2019-08
• Last Update Submitted: 2019-09-10
• Last Update Posted: 2019-09-11
• Primary Completion: 2022-03-31
• Study Completion: 2022-03-31

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Subjects with age more than 20
• Subjects obtained the consent
• Subjects with Parkinson disease and healthy subjects

Exclusion Criteria

• The subjects who can not conduct the tasks
• Subjects with severe illness
• Subjects whom the experimenter think as in appropriate
• Subjects with implantable devices such as pacemaker

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Training with Neurofeedback	Training with Neurofeedback	-
The other Training with Neurofeedback	The other Training with Neurofeedback	-

Primary Outcome Measures

Name	Time	Method
Alteration of Brain Activities	At the time Immediately following the training	measured by magnetoencephalography

Secondary Outcome Measures

Name	Time	Method
The raw score change from baseline in the Movement disorder society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS) part Ⅲ scores	At the time Immediately following the training	MDS-UPDRS retains the four-scale structure with a reorganization of the various subscales. The scales are now titled; (Part I) nonmotor experiences of daily living (13 items), (Part II) motor experiences of daily living (13 items), (Part III) motor examination (18 items), and (Part IV) motor complications (six items). Each subscale now has 0-4 ratings, where 0 = normal, 1 = slight, 2 = mild, 3 = moderate, and 4 = severe.; The total score is the sum of the subscale scores for Part III and ranges from 0 (no disability) to 132 (total dependence).

Trial Locations

Locations (1)

Osaka University; 🇯🇵 Suita-City, Osaka-fu, Japan