- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04288024
The Learning Effects of Task-priority Strategy on Dual-task Weight Shifting and Brain Plasticity in Patients With Parkinson's Disease
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Taipei, Taiwan
- National Taiwan University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 1. modified H-Y stage II-III Parkinson's disease 2. No other diseases 3. Non-demented PD 4. Non-tremor PD
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Postural
During training, participants in this group are instructed to focus on their posture during weight-shifting.
|
Postural task: Participants are standing with their weak side on the force plate. During the task, they wight-shift from side to side ranging from 10 to 90 percent of their body weight. Suprapostural task: Participants hold a tray with their arms beside the body, 90 degrees of elbow flexion. They rotate the tray left and right for 45 degrees respectively. During their task, participants should weight-shift and rotate the tray at the same time. |
Experimental: Suprapostural
During training, participants in this group are instructed to focus on their suprapostural task during weight-shifting.
|
Postural task: Participants are standing with their weak side on the force plate. During the task, they wight-shift from side to side ranging from 10 to 90 percent of their body weight. Suprapostural task: Participants hold a tray with their arms beside the body, 90 degrees of elbow flexion. They rotate the tray left and right for 45 degrees respectively. During their task, participants should weight-shift and rotate the tray at the same time. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
EEG relative power in the delta band
Time Frame: 60 minutes
|
postural and suprapostural performance of a dual task
|
60 minutes
|
EEG relative power in the theta band
Time Frame: 60 minutes
|
postural and suprapostural performance of a dual task
|
60 minutes
|
EEG relative power in the alpha band
Time Frame: 60 minutes
|
postural and suprapostural performance of a dual task
|
60 minutes
|
EEG relative power in the beta band
Time Frame: 60 minutes
|
postural and suprapostural performance of a dual task
|
60 minutes
|
EEG relative power in the gamma band
Time Frame: 60 minutes
|
postural and suprapostural performance of a dual task
|
60 minutes
|
COP trajectory recorded from the force plate
Time Frame: 60 minutes
|
performance of the postural task
|
60 minutes
|
Angles from inclinometer
Time Frame: 60 minutes
|
performance of the suprapostural task
|
60 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Gait velocity from GAITRite
Time Frame: 5 minutes
|
gait performance
|
5 minutes
|
Cadence from GAITRite
Time Frame: 5 minutes
|
gait performance
|
5 minutes
|
Mean step length from GAITRite
Time Frame: 5 minutes
|
gait performance
|
5 minutes
|
Step-to-step variability from GAITRite
Time Frame: 5 minutes
|
gait performance
|
5 minutes
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201907085RIND
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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