- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02390557
Persons With Disabilities Generating Quality Metrics
Persons With Disabilities Generating Quality Metrics to Inform Integrated Care
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
The aims of the project are as follows:
To work with persons with significant physical disabilities and serious and persistent mental illness to develop two new approaches to assess quality of care:
Approach #1: We will survey enrollees about their experiences in One Care and their thoughts about the care they receive. This survey will also ask One Care enrollees about how they manage their care and what self-direction means to them. The survey will be called the Persons with Disabilities Quality Survey (PDQ-S), and it will be available in English and Spanish versions.
Approach #2: Enrollees in One Care will provide information about their perceptions of care quality to a trained team of persons with disabilities who will report the information to One Care care teams. The goal of the activity is to support quality improvement in One Care through hearing the consumer's voice. This is called YES Health - Your Experience: Speak up for better health care.
- We want to test how providing consumer informed and consumer directed quality information to One Care providers affects One Care quality.
- We want to improve the ability of One Care enrollees to manage their own health care and to recognize and report quality problems
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- One Care enrollee
- Permanent physical disability and/or serious mental illness
- Seen at designated practice site
- English or Spanish speaking
Exclusion Criteria:
- Persons with an intellectual or a developmental disability
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Sundhedstjenesteforskning
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Ingen indgriben: Control - Standard Practice
Standard measures of quality at baseline.
No intervention reports sent to providers
|
|
|
Eksperimentel: Survey
Persons with Disabilities Quality Survey.PDQS Survey Reports Intervention.reports
sent to providers of OneCare enrollees
|
PDQS survey reports only
|
|
Eksperimentel: YESHealth
Arm 3: YESHealth Reports and PDQS Survey Reports sent to providers of OneCare enrollees
|
PDQS survey reports only
Arm 3: YESHealth and PDQS survey reports to providers
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Improved Quality of Care
Tidsramme: 12 months
|
% who agree that their quality of care Is better, the same or worse than before
|
12 months
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: Lisa I Iezzoni, MD, MSc, Mongan Institute Health Policy Center, Massachusetts General Hospital
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
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 (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 2014000899
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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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