A 60-seconds Personalized Mindfulness Video Exercise for Patients With Orthopedic Illness
The purpose of this study is to determine within a randomized controlled trial the feasibility of a 60-second acceptance based mindfulness exercise for patients with musculoskeletal pain versus usual medical care. Feasibility will be evaluated as the number of individuals approached who agree to participate and the number of individuals who drop out prior to completion of post intervention questionnaires.
The investigators aim to determine the usefulness and acceptability of the 60-second acceptance based mindfulness exercise for patients with musculoskeletal pain as compared to usual medical care. Usefulness and acceptability will be assessed with the Client Satisfaction Scale-3 (CSQ-3).
The investigators also aim to determine whether participating in a personalized 60-second acceptance based mindfulness exercise (e.g., intervention) is associated with significantly more improvement in patients' ratings of state anxiety and pain intensity (co-primary outcomes), and to determine if Distress, Anxiety, Depression and Anger (secondary outcomes) decrease compared to a brief educational pamphlet (e.g., control).
The investigators also aim to determine whether any improvements observed will maintain within a 3 month follow up.
調査の概要
詳細な説明
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
-
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Massachusetts
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Boston、Massachusetts、アメリカ、02114
- Massachusetts General Hospital
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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
説明
Inclusion Criteria:
- All patients presenting to Hand and Upper Extremity Service at Massachusetts General Hospital
- English fluency and literacy
Exclusion Criteria:
- Pregnant women
- Significant Axis I or II psychopathology that would interfere with participation in the study
- Age < 18 years old
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:支持療法
- 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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アクティブコンパレータ:60 Second Video
The mindfulness intervention is a video-flash found at http://www.pixelthoughts.co.
In this exercise patients are asked to write down a concern or worry, and watch it get put into perspective within a 60 seconds time frame.
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The mindfulness intervention will be a video-flash found at http://www.pixelthoughts.co.
In this exercise patients are asked to write down a concern or worry, and watch it get put into perspective within a 60 seconds time frame.
|
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他の:Educational Pamphlet
The educational pamphlet contains information about pain and stress, which patients will be able to read within 60 seconds.
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The educational pamphlet will contain information about pain and stress, which patients will be able to read within 60 seconds.
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 |
|---|---|---|
|
Client Satisfaction Scale-3 (CSQ-3)
時間枠:Day 1 after completing 60-second intervention
|
The client satisfaction scale-3 (CSQ-3) is a 3 question instrument to measure satisfaction with health and human services.
Responses are based on a 4-point scale.
The score range is from 3-12, where higher values indicate higher satisfaction.
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Day 1 after completing 60-second intervention
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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 State-Trait Anxiety Inventory (STAI)
時間枠:Before intervention, immediately after intervention, and 3 months after enrollment
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The STAI questionnaire measures trait and state anxiety.
The questionnaire has 20 items based on a 4-point scale.
A higher score is indicative of greater anxiety.
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Before intervention, immediately after intervention, and 3 months after enrollment
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Change in Pain Intensity
時間枠:Before intervention, immediately after intervention, and 3 months after enrollment
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Pain intensity as measured by ordinal rating of pain.
On a scale from 0-10, where 0 is no pain and 10 is the worst pain imagined.
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Before intervention, immediately after intervention, and 3 months after enrollment
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Change in Distress, Anxiety, Depression, and Anger
時間枠:Before intervention, immediately after intervention, and 3 months after enrollment
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A visual scale using 4 emotional thermometers to measure each distress, anxiety, depression, and anger.
The scale is from 0-10, where 0 means experience none of the emotion and 10 is extreme.
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Before intervention, immediately after intervention, and 3 months after enrollment
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協力者と研究者
出版物と役立つリンク
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 (実際)
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
- 2015P002349
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?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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。
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