- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04137952
Short-term Postural Training for Older Adults (P)
November 10, 2023 updated by: National Cheng-Kung University Hospital
The Use of Neuro-cognitive Strategies to Power Generalization Effect After Short-term Postural Training for Older Adults
Generalization refers to skill transfer under various working spaces following motor practice.
The extent of generalization effect links causal to in-depth recognition of error properties during motor practice.
Idiom says "imperfect practice makes perfect".
It could be beneficial for the elderly to gain superior capacity of balance transfer skill under the short-term productive failure learning environments.
In contrast to traditional visual feedback that uses error avoidance training to optimize target balance task, the present 3-year proposal is to propose three potential neuro-cognitive strategies to improve motor skill transfer following stabilometer training.
The strategies are expected to enhance opportunities of error experience and motor exploration via modified visual feedback, underlying facilitations of attentional resource and error-related neural networks.
In the first year, the neuro-cognitive strategy for balance practice is progressive augmentation of visual error size to improve balance skill transfer.
In the second year, the neuro-cognitive strategy for balance practice is visual feedback with virtual uncertainness of motor goal.
In the third year, the neuro-cognitive strategy for balance practice is stroboscopic vision.
EEG and central of pressure will be processed with non-linear approaches.
Graph theory will characterize EEG functional connectivity and brain network efficiency regarding to brain mechanisms for practice-related leaning transfer.
Trajectories of central of pressure will be analyzed with stabilogram diffusion analysis to reveal behavior mechanisms for practice-related variations in feedback and feedforward process for error corrections.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
150
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Eastern District
-
Taian, Eastern District, Taiwan, 701
- National Chen Kong University Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
60 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Age above 60 years old healthy older adults without a history of falls.
- Able to understand and give informed consent.
- The Mini-Mental State Examination test score above 25-30.
- Lower limb muscle strength is evaluated as G grade
- The corrected visual acuity was within the normal range.
Exclusion Criteria:
- Any known history of mental illness
- Any neuromuscular or degenerative neurological disease(ex:stroke、SCI、TBI...etc)
- Any known history of cerebral cerebellar disease or intracranial metal implants.
- Weak of hearing or wearing a hearing aid
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: deterministic visual error gain
Day1(Pretest):
Day2 to Day5:
Day6 (Posttest):
|
The strategies are expected to enhance opportunities of error experience and motor exploration via modified visual feedback, underlying facilitations of attentional resource and error-related neural networks.
Other Names:
|
Experimental: stochastic visual noise
Day1(Pretest):
Day2 to Day5:
Day6(Posttest):
|
The strategies are expected to enhance opportunities of error experience and motor exploration via modified visual feedback, underlying facilitations of attentional resource and error-related neural networks.
Other Names:
|
Experimental: intermittent visual gain
Day1 (Pretest):
Day2 (training section):
Day3 (Posttest):
|
The strategies are expected to enhance opportunities of error experience and motor exploration via modified visual feedback, underlying facilitations of attentional resource and error-related neural networks.
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
EEG graph analysis
Time Frame: through study completion, an average of 1 year
|
Graph theory will characterize EEG functional connectivity and brain network efficiency regarding to brain mechanisms for practice-related leaning transfer.
|
through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
stabilogram diffusion analysis of central of pressure
Time Frame: through study completion, an average of 1 year
|
Trajectories of central of pressure will be analyzed with stabilogram diffusion analysis to reveal behavior mechanisms for practice-related variations in feedback and feedforward process for error corrections.
|
through study completion, an average of 1 year
|
root mean sqaure error of stabilometer
Time Frame: through study completion, an average of 1 year
|
The root-mean-square value of the tracking trajectory of stabilometer and the target signal.
|
through study completion, an average of 1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Study Chair: Hwang Ing-Shiou, Phd, NCKU, Institute of Allied Health Sciences
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 1, 2019
Primary Completion (Actual)
December 30, 2022
Study Completion (Actual)
December 30, 2022
Study Registration Dates
First Submitted
October 20, 2019
First Submitted That Met QC Criteria
October 22, 2019
First Posted (Actual)
October 24, 2019
Study Record Updates
Last Update Posted (Estimated)
November 13, 2023
Last Update Submitted That Met QC Criteria
November 10, 2023
Last Verified
June 1, 2021
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- MOST 108-2314-B-006-071 -
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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