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Incentives for Primary Care Use in a Safety Net Setting

11. juni 2018 opdateret af: Virginia Commonwealth University

Incentives for Primary Care Use: A Randomized Controlled Trial in a Safety Net Setting

A randomized controlled trial (RCT) of incentives for an initial primary care visit within 6 months of enrollment in a health care coverage program. Study subjects are drawn from a low-income adult population that gains coverage and access to community-based primary care services under a program administered by an academic safety-net hospital. The investigators will offer financial incentives to encourage an initial primary care visit within 6 months of enrollment and evaluate whether the primary care visit altered subsequent health seeking behavior and influenced patient satisfaction and other outcomes such as self-reported health status.

Studieoversigt

Detaljeret beskrivelse

A randomized controlled trial (RCT) of incentives for an initial primary care visit within 6 months of enrollment in a health care coverage program. Study subjects are drawn from a low-income adult population that gains coverage and access to community-based primary care services under a program administered by an academic safety-net hospital. The investigators will offer financial incentives to encourage an initial primary care visit within 6 months of enrollment and evaluate whether the primary care visit altered subsequent health seeking behavior and influenced patient satisfaction and other outcomes such as self-reported health status.

Incentives should steer patients in their decision to seek primary care, reduce barriers to care, and ultimately improve patient health and reduce utilization and costs through their relationship with a PCP. This study is the first of its kind to incentivize low-income patients. This population has the greatest need for health care and exerts the greatest pressure on the United States' safety net system. Furthermore, the safety net population is the target of policies such as Medicaid eligibility expansions, yet urban safety net patients are largely understudied. These patients are rarely given the opportunity to participate in research, and when they are the subjects of measures to reduce health care utilization, they are the subject of policies using negative incentives such as those that introduce cost sharing for using ED services.1 Alternatively, safety net providers invest in case management systems to reduce utilization. The proposed study is a departure from prior measures to reduce utilization among low-income patients by focusing on patients and using positive incentives. The study borrows from the principles of behavioral economics to motivate patients towards primary care utilization. Once in the primary care system, The investigators will test whether primary care contact reduces more expensive forms (e.g., inpatient, ED) of health care.

The investigators will compare outcomes of patients assigned in the highest incentive group ($50) to patients assigned to the modest incentive group ($25) and to patients assigned to usual care (no incentive, but assignment to a PCP). The investigators will also compare incentive patients ($50, $25) to a contemporaneous group of patients that enroll in the safety net clinic at the same time.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

1228

Fase

  • Ikke anvendelig

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

21 år til 64 år (Voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Adults between ages 21-64 years
  • No prior enrollment in VCC for the past 12 months
  • English or Spanish speaking, and
  • Can be contacted by mail and telephone (preferably) or willing to be interviewed in person.

Exclusion Criteria:

  • Unable to be contacted by phone/mail
  • Cannot provide consent
  • No longer located in catchment area

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Sundhedstjenesteforskning
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Ingen indgriben: Contemporaneous Control
This group is our 'usual care' control group. They were not contacted for an interview and were not offered an incentive to visit their primary care physician.
Aktiv komparator: $0 group
This group completed a baseline interview but was not offered any incentive if they visited their primary care physician.
Those assigned to the $0 group will not receive an incentive for visiting their PCP.
Eksperimentel: $25 group
This group completed a baseline interview and was offered $25 they visited their primary care physician within 6 months.
Those assigned to the $25 group will receive $25 if they visit their PCP within 6 months of study enrollment.
Eksperimentel: $50 group
This group completed a baseline interview and was offered $50 they visited their primary care physician within 6 months.
Those assigned to the $50 group will receive $50 if they visit their PCP within 6 months of study enrollment.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
The number of Primary Care Physician visits will be assessed using medical claims record data.
Tidsramme: This will be assessed in the 6 months following study enrollment.
The number of primary care visits to a primary care physician will be collected from medical claims record data.
This will be assessed in the 6 months following study enrollment.

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
The time to a Primary Care Physician will be assessed using medical claims record data.
Tidsramme: This will be assessed in the 6 months following study enrollment.
The time to a primary care visits to a primary care physician will be collected from dates available in the medical claims record data.
This will be assessed in the 6 months following study enrollment.

Samarbejdspartnere og efterforskere

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

Efterforskere

  • Ledende efterforsker: Cathy Bradley, Phd, PI

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. januar 2014

Primær færdiggørelse (Faktiske)

8. november 2016

Studieafslutning (Faktiske)

8. november 2016

Datoer for studieregistrering

Først indsendt

28. september 2016

Først indsendt, der opfyldte QC-kriterier

3. oktober 2016

Først opslået (Skøn)

4. oktober 2016

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

12. juni 2018

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

11. juni 2018

Sidst verificeret

1. juni 2018

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • HM20000002
  • 1R01HS022534 (U.S.A. AHRQ bevilling/kontrakt)

Plan for individuelle deltagerdata (IPD)

Planlægger du at dele individuelle deltagerdata (IPD)?

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 .

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