- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01773577
The Effect of Interoperable Health IT on Efficiency in Ambulatory Practices (HEAL5)
Goal: To evaluate the effects of Interoperable Health IT on provider work flow and work practices in the ambulatory care setting.
Interoperable health IT can produce a reduction of barriers in the exchange of health information that can allow for more efficient, timely, and a higher quality of patient care. This study seeks to evaluate the effects of the implementation of interoperable health IT on the work flow of medical providers in the care environments in which they are implemented.
Studieoversigt
Status
Betingelser
Detaljeret beskrivelse
Interoperable health IT allows for the reduction of barriers in the exchange of health information. Substantial work flow efficiencies and cost reductions may be realized by reducing these barriers, and integrating information exchange among different providers and healthcare systems. Some of the avenues in which these efficiencies and cost reductions are likely to be achieved are through easier access to test results, reduction in medication errors, quality monitoring and improvement methodologies, and increased consumer choice. In recognition of the potential for these improvements, New York State has provided funding to regional entities (Regional Health Information Organizations-RHIO'S) whose role is to assist practice providers in the development, implementation, and integration of these interoperable IT systems. New York State has also provided funding to evaluate the technology implementations facilitated by the RHIOs. The investigators will be working with health care providers that have been assisted by the Greater Rochester RHIO.
Depending on the unique characteristics of the hardware and software that is developed and implemented, there may be variations in operational flow that effect efficiency in the ambulatory care setting. The goal of our study is to measure and evaluate the effects of interoperable IT systems in the work flow practices of providers that have implemented them in the ambulatory care setting.
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
-
-
New York
-
Rochester, New York, Forenede Stater, 14642
- University of Rochester
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- Our population will include all of the providers and office workers within the ambulatory care settings that have implemented the interoperable IT programs, and are required to utilize the systems for their daily job functions. Our research population will not include patients, as the participants of our study are the health care workers.
Exclusion Criteria:
- Our population will be "all inclusive" of all office staff and providers that are required to utilize the systems in place in order to perform their day-to-day functions. There will be no exclusions except for those under 18 years of age, and non English speakers (neither of which are expected to be in the eligible population).
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
|---|
|
Physician Pract. Employee and Off. Staff
The office staff and providers and physician practices enrolled in the RHIO
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Change in workflow pattern
Tidsramme: Day 1
|
Day 1
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Peter W Crane, MD, MBA, University of Rochester
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- HITEC/HEAL5
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Operations Research Workflow
-
Seva Canada SocietyPragyaan Sustainable Health Outcomes Foundation; Pushpagiri Vitreo Retina...RekrutteringKvalitetsforbedring | Aftaler og tidsplaner | Operations Research WorkflowIndien
-
University Hospital, GenevaRekruttering
-
Misr International UniversityAfsluttetAnmeldelse, Research PeerEgypten
-
University of Missouri-ColumbiaAfsluttet
-
Brigham and Women's HospitalPartners Siemens Research CouncilAfsluttetKontinuitet i patientbehandlingen | Workflow | Kvalitet af SignoutForenede Stater
-
University Hospital, Basel, SwitzerlandAfsluttetLaparoskopi | Kolecystektomi | Omkostninger | WorkflowSchweiz
-
Tata Memorial CentreIkke rekrutterer endnuProfessionel rolle | Research Peer Review
-
National Cheng-Kung University HospitalAfsluttetMeddelelse | Kvaliteten af sundhedsvæsenet | WorkflowTaiwan
-
University of MinnesotaNational Institute on Minority Health and Health Disparities (NIMHD); S...AfsluttetTeenagers sundhed | Ungdomsskoleforbundethed | Community Based Participatory Research MethodsForenede Stater
-
Elem YorulmazAktiv, ikke rekrutterendeSunde unge voksne, der er sundhedspersonale på Haydarpaşa Numune Training and Research HospitalKalkun