Access to a Sit-stand Computer Workstation and Back Pain
2017年10月6日 更新者：Kathleen Horst、Stanford University
Evaluating Change in Back Pain From Access to a Sit-stand Workstation
The purpose of the study is to evaluate the changes in back pain from access to a sit-stand workstation.
Other muscle and joint pain and/or discomfort will also be evaluated.
We hypothesize that access to a sit-stand workstation will allow one to experience postural variation and reduce back pain.
調査の概要
研究の種類
介入
入学 (実際)
57
段階
- 適用できない
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
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California
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Stanford、California、アメリカ、94305
- Stanford University
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
18年歳以上 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
Inclusion Criteria:
- Back pain lasting ≥3 months and reported at a minimum of 4 out of 10 on the pain scale.
- Sits >6 hours out of an 8-hour work day for work purposes
- Able and willing to fill out a daily survey for the first week prior to randomization
- Participants must be >18 years of age. There are no gender/race-ethnic restrictions.
- Ability to understand and the willingness to sign a written informed consent document.
Exclusion Criteria:
- Unable to stand for at least 10 minutes.
- Currently using a sit-stand desk
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
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：処理
- 割り当て：ランダム化
- 介入モデル：並列代入
- 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 |
|---|---|
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介入なし：Control
Did not receive an intervention during the active portion of the study (i.e. 12 weeks).
After the active portion of the study, this group was given a sit-stand computer workstation.
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実験的：Sit-stand computer workstation
Given a sit-stand computer workstation to use at their place of work
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A sit-stand computer workstation allows one to sit or stand throughout the day while maintaining continued use of one's computer.
他の名前：
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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 |
|---|---|---|
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Change in Back Pain
時間枠：Baseline (Week 1) and Follow-Up (Week 18)
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The Roland-Morris Disability Questionnaire is designed to assess self-rated physical disability caused by low back pain.
The patient is asked to agree or disagree with 24 different statements related to their back pain.
The end score is the sum of the agreed statements.
The score ranges from 0 (no disability) to 24 (maximum disability).
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Baseline (Week 1) and Follow-Up (Week 18)
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Change in Pain in Other Body Parts
時間枠：At the conclusion of each work day for 12 weeks and 8 weeks later
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The Brief Pain Inventory (BPI) allows patients to rate the severity of their pain and the degree to which their pain interferes with common dimensions of feeling and function.
This data was not analyzed due to the focus of the project on lower back pain.
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At the conclusion of each work day for 12 weeks and 8 weeks later
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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
捜査官
- 主任研究者：Kathleen C Horst, MD、Stanford University
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
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研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始
2013年4月1日
一次修了 (実際)
2013年12月1日
研究の完了 (実際)
2014年3月1日
試験登録日
最初に提出
2014年5月21日
QC基準を満たした最初の提出物
2014年5月21日
最初の投稿 (見積もり)
2014年5月23日
学習記録の更新
投稿された最後の更新 (実際)
2017年11月6日
QC基準を満たした最後の更新が送信されました
2017年10月6日
最終確認日
2017年10月1日
詳しくは
本研究に関する用語
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。