Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Post-Acute Physician Home Visit Program

9. august 2019 opdateret af: Jeffrey L. Schnipper, MD.,MPH., Brigham and Women's Hospital

Post-Acute Physician Home Visits: A Randomized Controlled Trial

New or worsening symptoms following discharge from the hospital likely leads to unplanned readmission. These rates are higher than desired and costly to patients, payers, and providers. Many interventions have unsuccessfully attempted to reduce readmissions, but few have provided in-home personnel to patients transitioning from acute care back to ambulatory care. Still fewer have involved a physician in the home. We therefore will test the effect of a physician home visit to a patient's home who was discharged in the last 4 days.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

51

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiesteder

    • Massachusetts
      • Boston, Massachusetts, Forenede Stater, 02115
        • Brigham and Women's Hospital
      • Boston, Massachusetts, Forenede Stater, 02130
        • Brigham and Women's Faulkner Hospital

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:

  • Resides within either a 5-mile or 20-minute driving radius of Brigham and Women's Hospital (BWH) or Brigham and Women's Faulkner Hospital (BWFH) emergency room
  • Has capacity to consent to study
  • >=18 years old

Exclusion Criteria:

  • Undomiciled
  • In police custody
  • Domestic violence screen positive

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Støttende pleje
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Home visit
A participant in this arm will receive a home visit after discharge from the hospital.

The visit will be entirely patient tailored, last approximately one hour, and at a minimum will entail:

  • Medical assessment
  • Psychosocial assessment
  • Medication reconciliation
  • Follow-up of inpatient primary team's specific recommendations
  • Follow-up, as needed, with primary care team or inpatient team
Ingen indgriben: Usual Care
A participant in this arm will not receive a home visit after discharge from the hospital.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
New or worsening symptoms
Tidsramme: 30 days after discharge from hospital

"Since you got home from the hospital, have you had any symptoms at all?" If no, stop. If yes, continue.

"I'm going to read off a list of symptoms, and I want you to tell me if that symptom is new or has gotten worse since you left the hospital. Please don't include symptoms that have stayed the same since you were in the hospital." For each affirmative, double check if the symptom is new or has gotten worse since getting out of the hospital. Only if new or worse, mark yes.

30 days after discharge from hospital

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
3-element Care Transition Mål, score
Tidsramme: 30 dage efter udskrivelsen
30 dage efter udskrivelsen
Total cost, 30-days post discharge
Tidsramme: Day of discharge to 30 days later
Day of discharge to 30 days later
Total reimbursement, 30-days post discharge
Tidsramme: Day of discharge to 30 days later
Day of discharge to 30 days later
Primary care provider follow-up within 14 days, y/n
Tidsramme: Day of discharge to 14 days later
Day of discharge to 14 days later
Ability to carry out the discharge plan, score
Tidsramme: 30 days after discharge
I would like to ask you about some more problems that you might have faced after you left the hospital one month ago. I will read some statements and ask if you agree or disagree.
30 days after discharge
Change in medication list due to home visit, y/n
Tidsramme: Day of home visit
Physician-initiated medication change during home visit
Day of home visit
Receipt of prescribed medicines following discharge, y/n
Tidsramme: 30 days after discharge
Pharmacy confirmation
30 days after discharge
Unplanned 30-day readmission(s) after index hospitalization, y/n
Tidsramme: 30 days after discharge
30 days after discharge
Unplanned 30-day readmission(s) after index hospitalization, #
Tidsramme: 30 days after discharge
30 days after discharge

Andre resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Global satisfaction with care, score
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Days at home since discharge, #
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
All-cause 30-day readmission(s) after index hospitalization, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
All-cause 30-day readmission(s) after index hospitalization, #
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Emergency Department (ED) observation stay(s) after index hospitalization, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Emergency Department (ED) observation stay(s) after index hospitalization, #
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Emergency Department (ED) visit(s) after index hospitalization, #
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Emergency Department (ED) visit(s) after index hospitalization, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Imaging, #
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Imaging, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Lab orders, #
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Lab orders, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Physician visits, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Physician visits, #
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Home health utilization, days
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Home health utilization, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
All cause 30-day mortality, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Unplanned 30-day mortality, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Change in medication list due to error at discharge, y/n
Tidsramme: Visit date
Exploratory
Visit date
Pneumococcal vaccination if appropriate, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Influenza vaccination if appropriate, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Smoking cessation counseling if appropriate, y/n
Tidsramme: 30 days after discharge
Exploratory
30 days after discharge
Evaluation of ejection fraction as assessed by echocardiogram or other appropriate study, scheduled or completed, if not done within 1 year; y/n
Tidsramme: 30 days after discharge
Heart failure patients only; Exploratory; appropriate studies include cardiac magnetic resonance imaging, radionuclide ventriculography, single photon emission computed tomography myocardial perfusion imaging, or left ventriculography
30 days after discharge
Angiotensin converting enzyme inhibitor or angiotensin receptor blocker for heart failure with reduced ejection fraction (ejection fraction < 40%), y/n
Tidsramme: 30 days after discharge
Heart failure patients only; Exploratory
30 days after discharge
Beta blocker for heart failure with reduced ejection fraction (ejection fraction < 40%), y/n
Tidsramme: 30 days after discharge
Heart failure patients only; Exploratory
30 days after discharge
Aldosterone antagonist for heart failure with reduced ejection fraction (ejection fraction < 40%), y/n
Tidsramme: 30 days after discharge
Heart failure patients only; Exploratory
30 days after discharge
Lipid lowering for coronary artery disease, peripheral vascular disease, cerebrovascular accident, or diabetes, y/n
Tidsramme: 30 days after discharge
Heart failure patients only; Exploratory
30 days after discharge
Smoking status post-discharge
Tidsramme: 30 days after discharge
Heart failure patients only; Exploratory
30 days after discharge
Use of inappropriate medications in the elderly, y/n
Tidsramme: 30 days after discharge
Exploratory; using Screening Tool of Older Persons' potentially inappropriate Prescriptions (STOPP) and Beers criteria
30 days after discharge
Time between discharge and visit, days
Tidsramme: Date of home visit
Exploratory
Date of home visit
Duration of physician visit, minutes
Tidsramme: Date of home visit
Exploratory
Date of home visit

Samarbejdspartnere og efterforskere

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

Efterforskere

  • Ledende efterforsker: Jeffrey Schnipper, MD MPH, Brigham and Women's Hospital

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

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 (Faktiske)

6. juni 2017

Primær færdiggørelse (Faktiske)

20. januar 2018

Studieafslutning (Faktiske)

20. januar 2018

Datoer for studieregistrering

Først indsendt

5. juni 2017

Først indsendt, der opfyldte QC-kriterier

5. juni 2017

Først opslået (Faktiske)

7. juni 2017

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

13. august 2019

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

9. august 2019

Sidst verificeret

1. august 2019

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • P000719

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

INGEN

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

Studerer et amerikansk FDA-reguleret lægemiddelprodukt

Ingen

Studerer et amerikansk FDA-reguleret enhedsprodukt

Ingen

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 Home visit

Abonner