Lido Workset Study
Assessment of Spasticity in MS Patients Using a Lido Workset
調査の概要
詳細な説明
The information gathered from testing individuals with spasticity due to multiple sclerosis with the Lido Workset has been important in making adjustments to the Lido Workset to show a greater degree of sensitivity in assessing varying degrees of spasticity.
Healthy control subjects will be used to compare the spasticity data of multiple sclerosis subjects with subjects with normal muscle tone to determine the sensitivity of the Lido measurements.
The testing will be performed one time for each patient and will take approximately 25 minutes. The servo-controlled torque motor system will analyze resistance to passive movement of the knee. This testing may be repeated for a group of randomly selected subjects from both the MS subjects and control subjects. The testing for this subset of subjects will be done as follows: first session, second session one week after the first session, third session three weeks after the first session. The total length of time for participation in this study may be up to three weeks. This additional testing will be done in order to compare the results with the Lido data obtained at similar timepoints from the subjects enrolled in the Cannabis for Spasticity in MS study. Each subject will be given the option to participate in the extended testing or to decline.
研究の種類
入学 (実際)
連絡先と場所
研究場所
-
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California
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Sacramento、California、アメリカ、95817
- University of California, Davis
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-
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
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Must have a diagnosis of multiple sclerosis and
- Must have some degree of spasticity or
- Must be a healthy control subject
- Ability to give informed consent
Exclusion Criteria:
- Patients with any life-threatening or unstable clinically significant disease
- Patients with other causes of reduced range of motion of the knee or wrist
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
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
|
Arm I
50 subjects with multiple sclerosis will be tested one time on the Lido Workset.
The test will take approximately 25 minutes.
The servo-controlled torque motor system will analyze resistance to passive movement of the knee.
This testing may be repeated for a group of randomly selected subjects.
Each subject will be given the option to participate in the extended testing or to decline.
The testing for this subset of subjects will be done as follows: first session, second session one week after the first session, third session three weeks after the first session.
The total length of time for participation in this study may be up to three weeks.
|
The intervention will consist of spasticity testing on the Lido Workset device.
The servo-controlled torque motor system will analyze resistance to passive movement of the knee.
|
|
Arm II
25 normal subjects will be tested on the Lido workset.
The testing will be performed one time for each patient and will take approximately 25 minutes.
The servo-controlled torque motor system will analyze resistance to passive movement of the knee.
This testing may be repeated for a group of randomly selected control subjects.
Each subject will be given the option to participate in the extended testing or to decline.
The testing for this subset of subjects will be done as follows: first session, second session one week after the first session, third session three weeks after the first session.
The total length of time for participation in this study may be up to three weeks.
|
The intervention will consist of spasticity testing on the Lido Workset device.
The servo-controlled torque motor system will analyze resistance to passive movement of the knee.
|
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 |
時間枠 |
|---|---|
|
Assess measure of spasticity
時間枠：3 weeks
|
3 weeks
|
協力者と研究者
捜査官
- 主任研究者：Mark Agius, MD、University of California, Davis
研究記録日
主要日程の研究
研究開始
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
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。