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Incentives for Primary Care Use in a Safety Net Setting

11. juni 2018 oppdatert av: 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.

Studieoversikt

Detaljert 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.

Studietype

Intervensjonell

Registrering (Faktiske)

1228

Fase

  • Ikke aktuelt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

21 år til 64 år (Voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Helsetjenesteforskning
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Ingen inngripen: 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.
Eksperimentell: $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.
Eksperimentell: $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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
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
Tiltaksbeskrivelse
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.

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Cathy Bradley, Phd, PI

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. januar 2014

Primær fullføring (Faktiske)

8. november 2016

Studiet fullført (Faktiske)

8. november 2016

Datoer for studieregistrering

Først innsendt

28. september 2016

Først innsendt som oppfylte QC-kriteriene

3. oktober 2016

Først lagt ut (Anslag)

4. oktober 2016

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

12. juni 2018

Siste oppdatering sendt inn som oppfylte QC-kriteriene

11. juni 2018

Sist bekreftet

1. juni 2018

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

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

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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