Posturography as Biomarker of Oculomotor and Postural Control Integration
調査の概要
詳細な説明
Subjects will undergo computerized dynamic posturography (CDP) testing using the extended modified Clinical Testing of Sensory Integration in Balance (ext_mCTSIB) protocol: the subjects will be required to stand on a hard or the compliant surface in a comfortable posture, feet shoulder width, with eyes open or closed, arms to the side and free to move, gazing forward, and breathing normally, with head straight, turned right or left, flexed or extended. This testing will be used to determine the health status of the subjects.
Then a sequence of tests will be performed (they could be done in different days to avoid fatiguing the subject): each sequence will comprise of a baseline test in one of the ext_mCTSIB testing conditions and a subsequent test in the same conditions but with an oculomotor additional task, such as gazing in a specific direction other than straight, performing saccades in different directions, at different speed and using different paradigms (prosaccades, antisaccades, to a remembered target, gap saccades, …), following a target moving on the screen at different speed and in different directions, receiving an optokinetic stimulation in different directions and at different speeds. Video recordings of the eyes movement may be done to make sure that the subject is actually moving the eyes, to verify that the observers are well trained to detect and count the saccadic movements, as well as to obtain quantitative information regarding the eye movements per se.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Self assessed healthy subjects
Exclusion Criteria:
- subjects suffering from pathology known to affect balance
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:基礎科学
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:subjects
participant undergoing posturographic evaluation
|
subjects will undergo CDP testing using one of the ext_mCTSIB tests without (baseline) and with oculomotor task
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Stability Score
時間枠:immediately after data collection
|
The Stability Score (calculated as percentage ratio of the actual sway and the theoretical limit of stability) will be used to investigate if there is any difference between the test without and with oculomotor task.
Statistical tools such t-tests and correlation coefficients will be used to assess if there is a difference between the two tests
|
immediately after data collection
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
average velocity moment [mm^2/s]
時間枠:immediately after data collection
|
The average velocity moment (calculated as as the product of sway velocity path length) will be used to investigate if there is any difference between the test without and with oculomotor task.
Statistical tools such t-tests and correlation coefficients will be used to assess if there is a difference between the two tests
|
immediately after data collection
|
|
sway path length [mm]
時間枠:immediately after data collection
|
The sway path length (the distance traveled during the test) will be used to investigate if there is any difference between the test without and with oculomotor task.
Statistical tools such t-tests and correlation coefficients will be used to assess if there is a difference between the two tests
|
immediately after data collection
|
|
frequency content [Hz]
時間枠:immediately after data collection
|
The frequency content (calculated using FFT) will be used to investigate if there is any difference between the test without and with oculomotor task.
Statistical tools such t-tests and correlation coefficients will be used to assess if there is a difference between the two tests
|
immediately after data collection
|
協力者と研究者
捜査官
- 主任研究者:Paul Noone, PhD、Carrick Institute for Graduate Studies
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- CI-IRB-20160321002
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
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