- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01944202
Educational Intervention to Reduce Outpatient Inappropriate Transthoracic Echocardiograms
Reducing Outpatient Inappropriate Transthoracic Echocardiograms With An Educational Intervention: A Randomized Control Trial
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
The investigators designed a randomized, control trial of an AUC-based educational and feedback intervention designed to reduce the proportion of inappropriate TTEs in the cardiology and internal medicine outpatient practices at Massachusetts General Hospital. A random number generator divided 24 cardiology fellows and 88 internal medicine residents into control and intervention arms.
During the study, physicians in the intervention arm receive the following multi-faceted educational intervention on TTE appropriateness: 1) a lecture at the beginning of the study period, which describes the AUC for echocardiography and highlights common clinical scenarios for which outpatient TTEs are ordered, 2) an electronic "pocket card" via email that provides tips on appropriate ordering of TTEs, and 3) an individualized monthly feedback report that categorizes TTEs ordered over the preceding month. The feedback reports contain the number of TTEs ordered during the month and how many are classified as appropriate, inappropriate, or uncertain based on the 2011 AUC. A description of all inappropriate TTEs and the rationale for the inappropriate classification is provided. The physicians in the control arm have their TTE orders tracked and classified, but do not receive any feedback on their ordering behavior. While study participants are not blinded to which arm of the study they are in, they were blinded to which arm of the study their colleagues are in.
Prior to the start of the intervention, all study participants receive a knowledge assessment survey. The survey includes five case-based questions designed to assess knowledge of the AUC for TTE and also questions regarding attitudes toward diagnostic testing. Each participant also receives a post-study knowledge assessment survey.
The primary outcome measures in this study are the rate of inappropriate and appropriate TTEs. Secondary outcome measures include the number of TTEs ordered, common appropriate and inappropriate TTE indications, and pre- and post-study knowledge assessment scores among the study physicians.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Massachusetts
-
Boston, Massachusetts, Vereinigte Staaten, 02114
- Massachusetts General Hospital
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Kind
- Erwachsene
- Älterer Erwachsener
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Cardiovascular Medicine fellows at Massachusetts General Hospital
- Internal Medicine residents at Massachusetts General Hospital
Exclusion Criteria:
- Attending physicians
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Versorgungsforschung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Educational Intervention
Physicians in the intervention arm receive the following multi-faceted educational intervention on transthoracic echocardiogram appropriateness: 1) a lecture at the beginning of the study period, which describes the Appropriate Use Criteria (AUC) for echocardiography and highlights common clinical scenarios for which outpatient TTEs are ordered, 2) an electronic "pocket card" via email that provides tips on appropriate ordering of TTEs, and 3) an individualized monthly feedback report that categorized TTEs ordered over the preceding month.
The feedback reports contains the number of TTEs ordered during the month and how many are classified as appropriate, inappropriate, or uncertain based on the 2011 AUC.
|
Educational and feedback intervention, as described in the Arm Description.
|
|
Kein Eingriff: Control group
Physicians in the control arm have their TTE orders tracked and classified, but do not receive any feedback on their ordering behavior.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Rate of Inappropriate transthoracic echocardiograms
Zeitfenster: 9 months
|
Rate of inappropriate echocardiograms determined from a review of the electronic medical record.
|
9 months
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Rate of Appropriate Transthoracic Echocardiograms
Zeitfenster: 9 months
|
Rate of appropriate transthoracic echocardiograms determined from a review of the electronic medical record.
|
9 months
|
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Clinical reasons for appropriate and inappropriate transthoracic echocardiograms
Zeitfenster: 9 months
|
All echocardiograms will be classifed according to the Appropriate Use Criteria (AUC).
This will allow for determination of the most common clinical indications for both appropriate and inappopriate TTEs.
|
9 months
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Rory B Weiner, MD, Massachusetts General Hospital
Publikationen und hilfreiche Links
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
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
Andere Studien-ID-Nummern
- 2011P001779CR1
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 .
Klinische Studien zur Educational intervention
-
Mansoura UniversityUniversity of PittsburghAbgeschlossenSchizophrenie | Stigma, sozialÄgypten
-
University of Southern CaliforniaNational Cancer Institute (NCI)RekrutierungKolorektales KarzinomVereinigte Staaten
-
Hong Kong Metropolitan UniversityNoch keine RekrutierungPflegeunterrichtspädagogik | Konversations -KI -Krankenpflegeausbildung ernstes Spiel
-
Ziauddin UniversityUniversiti Sains MalaysiaNoch keine RekrutierungGingivitis | ZahnbelagPakistan
-
Oral Health Centre of Expertise in Western NorwayEducational storytelling forlag og filmAbgeschlossenKindesmissbrauch | Mundhygiene | Kindesvernachlässigung | Kindesmisshandlung | Sexueller Missbrauch von Kindern | Zahnärztliche VernachlässigungNorwegen
-
University of MichiganNational Heart, Lung, and Blood Institute (NHLBI)Abgeschlossen
-
Université de MontréalUnbekanntChirurgische Ausbildung | Fortgeschrittene Nähfähigkeiten
-
Hospital Israelita Albert EinsteinAbgeschlossenEvidenzbasierte PraxisBrasilien
-
University of WashingtonNational Institute of Mental Health (NIMH)RekrutierungAutismus-Spektrum-StörungVereinigte Staaten
-
University of Colorado, DenverCancer League of ColoradoNoch keine RekrutierungNeu diagnostizierter Brustkrebs | Brustkrebs bei FrauenVereinigte Staaten