- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT00542737
Evaluating a Web-Based Ventilator Management Educational Program for Clinicians (The Lung Injury Knowledge Network [LINK] Study) (LINK)
Improving Ventilator Management and Preventing Injury to Patients With Acute Respiratory Failure
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
ALI/ARDS is a life-threatening condition that involves inflammation of the lungs and fluid accumulation in the air sacs, leading to low blood oxygen levels and respiratory failure. Common causes include pneumonia, septic shock, and lung trauma, and most patients require immediate care in an ICU. The main form of treatment for ALI/ARDS is the delivery of oxygen and a continuous level of pressure to the damaged lungs through mechanical ventilation. Each year, 74,500 people die due to ALI/ARDS and 22% of these deaths could be prevented with the use of LPV. LPV is a mechanical ventilation technique in which lower volumes of oxygen are administered. The purpose of this study is to implement and evaluate a Web-based educational program that will provide educational and instructional resources about ALI/ARDS and LPV to ICU clinicians, including physicians, nurses, and respiratory therapists.
Hospitals participating in this study will be randomly assigned to access the Web site at either the beginning of the study period or a later time. Participating clinicians at each hospital will access the Web site as often as necessary for a 6-month period. The Web site will contain background and educational information on ALI/ARDS and LPV, including how to recognize ALI/ARDS and how to implement LPV in patients. Scholarly articles and other materials, including a chart to help clinicians determine appropriate ventilator settings for each patient, will be available to download. Clinicians will also be able to email questions to critical care experts. At the end of the 6-month study period, study staff will compare the number of patients receiving LPV to the number of patients who received LPV prior to the start of the study.
Studientyp
Einschreibung (Voraussichtlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Ontario
-
Toronto, Ontario, Kanada, M4N3M5
- University of Toronto, Sunnybrook Health Sciences
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria for Hospitals:
- Between 10 and 20 ICU beds with 5 to 10 ALI/ARDS patients cared for each month
- Provide critical care services
- Keep electronic medical records on ICU patients
- ICU staff must have access to computers with Intranet or Internet
Inclusion Criteria for Clinicians:
- Provide care for mechanically ventilated patients in ICUs
- Willing to participate by viewing Web site
Exclusion Criteria for Hospitals:
- Cardiac, cardiothoracic, neurosurgical, neonatal, or pediatric ICUs
- Residents and fellows must provide care to majority of critically ill patients
- Fewer than 5 to 10 ALI/ARDS patients cared for each month
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
---|---|
Aktiver Komparator: Early Intervention Group
|
Participating clinicians at each hospital will access the Web site as often as necessary for a 6-month period.
The Web site will contain background and educational information on ALI/ARDS and LPV, including how to recognize ALI/ARDS and how to implement LPV in patients.
Scholarly articles and other materials, including a chart to help clinicians determine appropriate ventilator settings for each patient, will be available to download.
Clinicians will also be able to email questions to critical care experts.
|
Aktiver Komparator: Delayed Intervention Group
|
Participating clinicians at each hospital will access the Web site as often as necessary for a 6-month period.
The Web site will contain background and educational information on ALI/ARDS and LPV, including how to recognize ALI/ARDS and how to implement LPV in patients.
Scholarly articles and other materials, including a chart to help clinicians determine appropriate ventilator settings for each patient, will be available to download.
Clinicians will also be able to email questions to critical care experts.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
---|---|
Percentage of eligible patients with ALI/ARDS who are receiving LPV
Zeitfenster: Measured at Month 6
|
Measured at Month 6
|
Mitarbeiter und Ermittler
Ermittler
- Hauptermittler: Gordon D. Rubenfeld, MD, University of Toronto, Sunnybrook Health Sciences
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Voraussichtlich)
Studienabschluss (Voraussichtlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 518
- R01HL067939 (US NIH Stipendium/Vertrag)
- GC1# A19846
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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