新型コロナウイルス感染症の看護師のパンデミック疲労と回復力を高めるオンラインマインドフルネスセラピー
2024年5月23日 更新者：Chimei Medical Center
新型コロナウイルス感染症隔離病棟の看護師のパンデミック疲労と回復力に対するオンラインマインドフルネス療法の効果を評価する
この研究では、オンラインマインドフルネス療法が新型コロナウイルス感染症（COVID-19）隔離病棟の看護師のパンデミック疲労と回復力に及ぼす影響を評価した。
60人の看護師が実験グループと対照グループに分けられ、実験グループは6週間のオンラインマインドフルネスコースを受けました。
調査の概要
詳細な説明
この研究では、新型コロナウイルス感染症（COVID-19）隔離病棟の看護師のパンデミック疲労の軽減と回復力の強化に対するオンラインマインドフルネス療法の有効性を評価しています。
反復測定の準実験計画を使用して、60 人の看護師が実験グループと対照グループに分けられました。
実験グループは6週間のオンラインマインドフルネスコースに参加しました。
テスト前、3週間後、6週間後に、パンデミックによる疲労と回復力に関するアンケートを使用して結果を測定しました。
研究の種類
介入
入学 (実際)
60
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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其他（非美國）
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Tainan City、其他（非美國）、台湾、71004
- Chi Mei Medical Center
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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
- 大人
- 高齢者
健康ボランティアの受け入れ
いいえ
説明
包含基準:
- 20歳以上。
- 新型コロナウイルス感染症専用病棟と専用集中治療室の看護師。
除外基準:
- 出席の困難さ
- オンラインマインドフルネスセラピーセッションの総数の80%未満
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：他の
- 割り当て：非ランダム化
- 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 |
|---|---|
|
実験的：実験グループは6週間のオンラインマインドフルネスコースを受講します
実験グループは、週に1回、各セッション90分の6週間のオンラインマインドフルネスコースを受けました。
参加者はコース前、第 3 週目、第 6 週目にアンケートに回答しました。
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実験グループは、週に1回、各セッション90分の6週間のオンラインマインドフルネスコースを受けました。
|
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介入なし：対照群
一般的な日常ケア
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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 |
|---|---|---|
|
パンデミック疲労
時間枠：6週間
|
ロックダウン/パンデミック疲労スケール (LFS) を使用してパンデミック疲労を測定します。
合計 10 項目のスケールでパンデミック疲労を測定します。
スケールの合計スコアの範囲は 10 ～ 50 です。
これは、スケールの合計ポイントが増加するにつれてパンデミック疲労が増加することを示しています。
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6週間
|
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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回復力
時間枠：6週間
|
Connor-Davidson Resilience Scale (CD-RISC) を使用して、個人の回復力を測定します。
合計 25 項目の尺度でレジリエンスを測定します。
スケールの合計スコアの範囲は 0 ～ 100 です。
スケールの合計ポイントが増加するにつれて、回復力が増加することを示しています。
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6週間
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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
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 (実際)
2022年10月1日
一次修了 (実際)
2023年5月31日
研究の完了 (実際)
2023年5月31日
試験登録日
最初に提出
2024年5月23日
QC基準を満たした最初の提出物
2024年5月23日
最初の投稿 (実際)
2024年5月29日
学習記録の更新
投稿された最後の更新 (実際)
2024年5月29日
QC基準を満たした最後の更新が送信されました
2024年5月23日
最終確認日
2024年5月1日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 11112-001
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?
いいえ
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
いいえ
米国FDA規制機器製品の研究
いいえ
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