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Use of Decision Aids in Clinical Encounters

23. maj 2016 opdateret af: Victor Montori, Mayo Clinic

Patient-centered Dissemination of Evidence-based Medicine: Share EBM

The active strategy for dissemination and implementation of Share Evidence Based Medicine (EBM) will yield greater reach of clinicians, be adopted by the practices more readily, and a greater uptake of use amongst encounters will be seen.

The Institute for Clinical Systems Improvement (ICSI) is a nonprofit organization with expertise in large-scale practice improvement at the state and national level. Largely funded by health organizations in Minnesota, ICSI has a sustainable model to translate evidence into practice, through clinical practice guidelines, shared decision making, and practice redesign. A partnership between these two organizations (ICSI and Mayo Clinic) may lead to a sustainable and innovative approach to the dissemination of evidence-based health information at the point of care.

The objective of the current study is therefore to leverage the expertise of these two organizations to compare the impact of an active to a passive dissemination and implementation strategy of the ShareEBM toolkit. The aim of the study is to disseminate evidence-based information through the use of decision aids during encounters. The overall purpose of the qualitative evaluation is to understand why decision aids were used more or less in certain practices and what factors contributed to or hindered this uptake.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

62

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • Minnesota
      • Brooklyn Center, Minnesota, Forenede Stater, 55430
        • Park Nicollet- Brookdale
      • Delano, Minnesota, Forenede Stater, 55328
        • Ridgeview Medical Center
      • Duluth, Minnesota, Forenede Stater, 55804
        • Essentia Health-Lakeside Clinic
      • Eagan, Minnesota, Forenede Stater, 55122
        • Fairview Clinic-Eagan
      • Golden Valley, Minnesota, Forenede Stater, 55427
        • Park Nicollet-Golden Valley
      • Hermantown, Minnesota, Forenede Stater, 55811
        • Essentia Hermantown Clinic
      • Minneapolis, Minnesota, Forenede Stater, 55404
        • Native American Community Clinic
      • Rochester, Minnesota, Forenede Stater, 55905
        • Mayo Clinic
      • Rochester, Minnesota, Forenede Stater, 55904
        • Community Health Service, Inc.
      • Rosemount, Minnesota, Forenede Stater, 55068
        • Fairview Medical-Rosemount
    • Wisconsin
      • Baldwin, Wisconsin, Forenede Stater, 54002
        • Baldwin Area Medical Center, Inc.
      • Hudson, Wisconsin, Forenede Stater, 54016
        • Hudson Physicians S.C.

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Practices meeting the following criteria will be deemed eligible for the study if they have:

    1. At least 2 primary care clinicians committed to participate in the study. Clinicians are defined as any healthcare professional providing patient care (i.e., physicians, nurse practitioners, physician assistants, diabetes educators)
    2. A designated site champion and support staff that can provide the support needed to conduct the study
    3. An IRB approval from their institution or are covered under Mayo Clinic IRB
    4. Leadership is committed to this research and has endorsed the study
  • Any clinician caring for patients with a chronic condition and who has opportunities to discuss medication management with their patients will be deemed eligible

Exclusion Criteria:

  • Major barriers to participating or to providing informed consent

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Andet: Active Implementation of Share EBM Toolkit
Investigators led implementation of tailored activities and tactics (Shared EBM Toolkit) designed to promote the use of the decision aids in clinical encounters (i.e. journal clubs, value map streaming).
Andet: Passive Implementation of Share EBM Toolkit
Locally supported dissemination of Shared EBM Toolkit designed to promote the use of the decision aids in clinical encounters.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Frequency of use of decision aids in clinical encounters by weekly reports
Tidsramme: up to 1 year
up to 1 year

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. september 2014

Primær færdiggørelse (Faktiske)

1. maj 2016

Studieafslutning (Faktiske)

1. maj 2016

Datoer for studieregistrering

Først indsendt

24. marts 2014

Først indsendt, der opfyldte QC-kriterier

8. maj 2014

Først opslået (Skøn)

12. maj 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

24. maj 2016

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

23. maj 2016

Sidst verificeret

1. maj 2016

Mere information

Begreber relateret til denne undersøgelse

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 Active Implementation of ShareEBM Toolkit

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