Continuous Vital Sign Monitoring in a Surgical Ward
Continuous Vital Sign Monitoring in a Norwegian Hospital Surgical Ward: A Multi-Method Study of Patient Outcomes, Patient Safety Culture, and Nursing Staff Experiences
Unsafe patient care remains a major contributor to global morbidity and mortality. In surgical wards, postoperative patients are typically monitored intermittently using the National Early Warning Score (NEWS-2), leaving periods during which clinical deterioration may go undetected. Continuous vital sign monitoring (CVSM) using wearable sensors offers the potential for earlier identification of deterioration compared with intermittent assessments.
CVSM was introduced in a hospital ward as part of a hospital-initiated pilot implementation and is used alongside standard monitoring with NEWS-2. The purpose of the study is to evaluate this implementation.
This observational study uses a pragmatic, quasi-experimental, multi-method, longitudinal design. The overall aims of the study are to evaluate the impact of CVSM implementation on patient outcomes, to explore healthcare professionals' perceptions of patient safety culture, turnover intention and pleasure of work, and to describe their experiences with implementation.
調査の概要
状態
詳細な説明
Unsafe care is a major contributor to global morbidity and mortality. In surgical wards, postoperative patients are typically monitored intermittently using the National Early Warning Score (NEWS-2), which may leave periods during which changes in vital signs go undetected, potentially increasing the risk of clinical deterioration. Continuous vital sign monitoring (CVSM) using wearable sensors may enable earlier detection of deterioration compared with intermittent monitoring.
This study evaluates the implementation of CVSM using 16 wearable sensors in a 29-bed gastro-surgical ward beginning in September 2025. CVSM is based on wearable sensors that continuously monitor patients' respiratory rate, heart rate, and oxygen saturation. The system transfers data to the electronic health record, and alerts are generated when predefined thresholds are exceeded and delivered to nursing staff via smartphones and workstation monitors. CVSM is implemented in addition to usual care, including intermittent NEWS-2 monitoring, in accordance with hospital protocol.
The intervention was implemented as part of a hospital-initiated pilot programme that was supported by hospital management and aimed to evaluate the feasibility and potential effects of broader CVSM adoption. The intervention ward was selected by the hospital for pragmatic reasons, based on managers' agreement to implement CVSM. Implementation was overseen by a hospital-appointed project manager. Members of the research team participated in implementation meetings and provided input on potential implementation strategies. However, responsibility for implementation decisions remained with hospital management and the clinical departments, and implementation was primarily guided by clinical priorities and operational constraints within the hospital. The primary role of the research team was to support and conduct the empirical evaluation of the intervention and its implementation.
It is hypothesised that CVSM may enable earlier detection of patient deterioration compared with intermittent monitoring alone and thereby influence patient outcomes. It is also hypothesised that CVSM may influence healthcare professionals' perceptions of patient safety culture, turnover intention, and work-related well-being. The study will further generate knowledge about healthcare professionals' experiences with the implementation.
While data collection for the studies on patient safety culture and nurses' experiences with implementation has started, the patient outcome study is currently awaiting a decision from the Norwegian Directorate of Health. Data collection for this study has not yet commenced. The studies on patient safety culture and nurses' experiences with implementation have been preregistered in the Open Science Framework (OSF).
研究の種類
入学 (推定)
連絡先と場所
研究連絡先
- 名前:Gørill H. Birkeli, PhD
- 電話番号:+47 47304895
- メール:gobi@ahus.no
研究場所
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Akershus
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Lørenskog、Akershus、ノルウェー、1478
- 募集
- Akershus University Hospital HF
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参加基準
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
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Patients aged 18 years or older admitted to the gastro-surgical ward.
- Healthcare professionals aged 18 years or older employed in the participating wards for survey participation.
- Nursing staff with at least 6 months of work experience and experience using CVSM for participation in qualitative focus group interviews.
Exclusion Criteria:
- Patients with delirium.
- Patients with cognitive impairment interfering with sensor use.
- Patients who decline participation.
- Patients with allergy to electrode adhesives.
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 |
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Intervention ward
All patients admitted to the gastro-surgical ward during the 12-month implementation of continuous vital sign monitoring (CVSM). Healthcare professionals (physicians, nursing assistants, and registered nurses) working predominantly in the intervention ward. |
The intervention consists of continuous vital sign monitoring (CVSM) using wearable sensors applied to patients.
A total of 16 sensors are implemented in a 29-bed gastro-surgical ward.
The system continuously records patients' vital signs and transfers data to the electronic health record.
Alerts are generated when predefined thresholds are exceeded and are delivered to nursing staff via smartphones and workstation monitors.
The intervention is implemented in addition to usual practice with intermittent monitoring using the National Early Warning Score (NEWS-2), according to hospital protocol.
Nursing staff receive training prior to implementation, and clinical responses to alerts are managed in accordance with hospital procedures.
The intervention was implemented from September 2025 and continues during the study period.
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Control group
All patients admitted to the same gastro surgical ward will be its own control group 1 year before the intervention.
Patients received standard care before the intervention.
This means that relevant outcomes during the implementation (2026) is compared to the same outcomes before the intervention (i.e., 2024) in the same ward.
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Non-equivalent comparison group
All patients admitted to a non-equivalent comparison ward for the period spanning from January 1, 2024, to January 1, 2025, and from October 1, 2025, to October 1, 2026, during which CVSM was not implemented. Healthcare professionals (physicians, nursing assistants, and registered nurses) working predominantly in a comparable gastro-surgical ward at the same hospital during the 12-month implementation period of CVSM in the intervention ward. |
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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NEWS-2 Associated with RRT Activation
時間枠:Up to 12 months after implementation
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National Early Warning Score 2 (NEWS2) associated with rapid response team (RRT) activation.
NEWS2 is a physiological deterioration score ranging from 0 to 20 points.
Higher scores indicate greater physiological deterioration and worse clinical status.
According to hospital protocol, RRT consultation is recommended at NEWS2 ≥7.
NEWS2 at the time of RRT activation will be assessed.
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Up to 12 months after implementation
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Patient Safety Culture (N-HSOPSC 2.0)
時間枠:Baseline, 5 months, and 12 months after implementation
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Healthcare professionals' perceptions of patient safety culture measured as changes in the ten composite dimensions and two single-item measures of the Norwegian Hospital Survey on Patient Safety Culture (N-HSOPSC 2.0).
Responses are recorded using 5-point Likert scales ranging from 1 to 5. Higher scores indicate more positive perceptions of patient safety culture.
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Baseline, 5 months, and 12 months after implementation
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Nursing Staff Experiences with CVSM
時間枠:Approximately 6 months after implementation
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Nursing staff experiences with the implementation and perceived usefulness of continuous vital sign monitoring (CVSM) for patient safety, explored through qualitative focus group interviews.
This is a qualitative outcome measure and no numerical score will be calculated.
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Approximately 6 months after implementation
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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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Rapid Response Team (RRT) Activation
時間枠:Up to 12 months after implementation
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Number of Rapid Response Team (RRT) activation
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Up to 12 months after implementation
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Unplanned Transfers to Higher Level of Care
時間枠:Up to 12 months after implementation
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Number of unplanned transfers to a higher level of care (intensive care unit or postoperative care unit)
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Up to 12 months after implementation
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Hospital Length of Stay
時間枠:Up to 12 months after implementation
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Total hospital length of stay (hours)
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Up to 12 months after implementation
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NEWS-2 at Time of Clinical Deterioration
時間枠:Up to 12 months after implementation
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National Early Warning Score 2 (NEWS2) measured at the time of unplanned transfer to a higher level of care.
NEWS2 is a physiological deterioration score ranging from 0 to 20 points.
Higher scores indicate greater physiological deterioration and worse clinical status.
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Up to 12 months after implementation
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Pleasure of Work and Turnover Intention
時間枠:Baseline, 5 months, and 12 months after implementation
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Healthcare professionals' perceived pleasure of work and turnover intention measured using validated composite measures.
Pleasure of work is assessed on a 4-point Likert scale (1-4) and turnover intention on a 5-point Likert scale (1-5).
Higher scores indicate greater pleasure of work and lower turnover intention.
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Baseline, 5 months, and 12 months after implementation
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協力者と研究者
捜査官
- 主任研究者:Gørill H. Birkeli, PhD、University Hospital, Akershus
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 (推定)
研究の完了 (推定)
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
キーワード
- 実装
- 遠隔監視
- 患者の安全
- 定性調査
- ウェアラブル デバイス
- デジタルヘルス
- 看護師
- 患者モニタリング
- 術後の患者さん
- ヘルスケアのプロ
- フォーカスグループインタビュー
- 患者の悪化
- 準実験的なデザイン
- 患者の安全文化
- Continuous vital sign monitoring
- Early warning scores
- National Early Warning Score (NEWS-2)
- Hospital Survey on Patient Safety Culture (HSOPSC 2.0)
- Employee motivation
- Work-related outcomes
- Technology implementation
- SEIPS
- Gastro-surgical ward
その他の研究ID番号
- CVSM-2026
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?
IPD プランの説明
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
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