Role of Provider-at-Triage on ED Efficiency and Quality of Care (MD at Triage)
Effects of Provider-at-Triage on Emergency Department Efficiency, Information Delivery and Patient Satisfaction
The United States spends over $8,000 per capita annually on health care and its health care system is more expensive than other developed countries. Even with high per capita costs and a high proportion of physician specialists, the US lags in health care performance from patients' perspectives.
The hospital emergency department (ED) is often the portal of entry for patients seeking health care services and is therefore an ideal setting for initiatives to improve efficiency of care delivery and patient satisfaction. Reduction in wait times, enhanced information delivery and ED staff service quality all have a positive influence on patient perception of health care quality and satisfaction.
Prior studies have attempted to increase patient satisfaction by improving staff communication and courtesy, implementing a patient satisfaction team in triage, and delivering information to patients in a timely manner. Another strategy to increase the efficiency of ED operations is adding a physician to triage to perform brief medical screenings and initiate necessary patient testing and treatment. This contrasts to usual practice in which physicians evaluate patients only following registration and nurse assessment of illness or injury severity.
調査の概要
状態
詳細な説明
This study will assess the impact of early patient assessment by a physician at Emergency Department (ED) triage on patient perception of information delivery, overall patient satisfaction and ED efficiency. ED efficiency will be assessed by ED length of patient stay, ED left-without-being-seen and ED left during treatment rates.
Participants who decide to take part in this study, will be asked questions by research staff, who will document responses on a secure iPAD device. The survey will ask participants how they feel about their health condition, the emergency department wait, the care they received in the emergency department and how satisfied the participant was with the care received.
研究の種類
入学 (実際)
連絡先と場所
研究場所
-
-
Florida
-
Gainesville、Florida、アメリカ、32608
- UF Health
-
-
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:
Participants are eligible to participate in the study if they are:
- English speaking
- Without hemodynamic or respiratory compromise
- Do not have a nurse-assigned triage severity score of Emergency Severity Index 1 (most severe illness or injury score).
Exclusion Criteria:
Participants will be excluded if they are:
- Unwilling or unable to sign an informed consent
- In police custody
- Too ill to participate in study.
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 |
|---|---|
|
Usual Care
Group enrolled during normal emergency department operating procedures (without a physician present at triage).
|
No physician at triage
|
|
Physician at Triage
Group enrolled while a physician is present at triage.
|
A physician embedded at triage
|
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 |
|---|---|---|
|
Patient Satisfaction
時間枠:60 minutes after Emergency Department triage
|
Patient Satisfaction Score- brief survey measured on a Likert Scale
|
60 minutes after Emergency Department triage
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Emergency Department efficiency
時間枠:24 hours after ED triage in minutes
|
Impact of physician at triage on ED length of stay rates
|
24 hours after ED triage in minutes
|
|
Left without being seen rate
時間枠:12 hours after ED triage in minutes
|
Impact of physician at triage on left without being seen rate
|
12 hours after ED triage in minutes
|
協力者と研究者
スポンサー
捜査官
- 主任研究者:Brandon Allen, MD、Univeristy of Florida
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
本研究に関する用語
その他の研究ID番号
- IRB201500586
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。