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Development and Validation of a Comprehensive Standardised Clinical Assessment Tool for Patient Needs (ACTI-PALLI)

17. maj 2016 opdateret af: Maison Médicale Jeanne Garnier
The purpose of this study is to develop and validate a comprehensive and standardised tool for assessment of patient needs in palliative care.

Studieoversigt

Status

Ukendt

Betingelser

Detaljeret beskrivelse

Rationale for the study

In France, around 150000 people require palliative care every year. Since 2002, palliative care has been organized at several levels: palliative care units, palliative care mobile support teams, health network for palliative care and home-based hospital care. These structures have made possible for some patients in need of palliative care to be treated in appropriate service, in facility-based or community-based programs. With these important advances around palliative care, it appears important to assess the quality of care provided to patients. However, no generalizable study has been conducted in France, and no formal tool is available to help at this end.

In order to enhance the effectiveness of these services, it is important to conduct studies with the aim of developing the adapted and standardized tools that will enable assessment of quality for palliative care, as well as its determinants, for example the organization of structures, management of teams, etc. To this end, it is relevant to adopt a more holistic perspective and take into account the views of different concerned people, including the patients, their families and healthcare professionals, all while considering the organizational and management aspects.

The evidence from other countries has demonstrated the necessity of a rigorous, exhaustive and systematic evaluation as a requirement for any palliative program of quality. Many tools have since been developed to assess the multidimensional needs of patients, but none of these tools have been adapted to be used in the French palliative care settings.

Among of different tools used in palliative care, InterRAI Palliative Care (RAI-PC) has been chosen as the most reliable and complete tool. The RAI-PC allows a comprehensive evaluation of patients, as well as capabilities, preferences and needs. The medical, psychological, functional and social indicators are defined. This tool has been applied in the palliative care field in Canada and USA, but not yet in France. It has proven itself as an appropriate tool for needs assessment and evaluation of quality of care.

Goals of the project

This project aims to develop and validate a comprehensive and standardized instrument that will serve:

  1. As a support to individual care, emphasizing the individual characteristics and needs of patients, informing planning care, outcome measurement, quality indicators, and case-mix classification.
  2. As a standardized assessment tool adaptable to various palliative care structures

Study design

This study is a multicenter, prospective, observational study with representative stratified sample from different categories of palliative care services: palliative care units, palliative care mobile support teams, health network for palliative care and home-based hospital care. Twenty-three palliative structures, spread across the country are participating in this project.

The survey will involve the healthcare professionals of each center, trained on collecting information and using InterRAI instrument. Data collection involves patient clinical assessment, reviewing medical and nurse record and interview with family and professionals of healthcare.

Criteria for judgement

The quality of the tool will be judged in terms of satisfactory of psychometric properties, operational characteristics and clinical acceptability, adaptability of the tool to the needs of patients and its relevance in different palliative care structures.

Undersøgelsestype

Observationel

Tilmelding (Forventet)

480

Kontakter og lokationer

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

Studiekontakt

Undersøgelse Kontakt Backup

Studiesteder

      • Paris, Frankrig, 75015
        • Rekruttering
        • Maison Médicale Jeanne Garnier
        • Kontakt:
        • Kontakt:
        • Ledende efterforsker:
          • Frédéric Guirimand

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

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

Patients receiving palliative care

Beskrivelse

Inclusion Criteria:

  • Men and Women, age ≥ 18 years
  • Patients receiving palliative care at home or in hospital at the time of screening

Exclusion Criteria:

  • Non consenting
  • Patient waiting a transfer within 48 hours

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Criterion-related validity: correlation between the score obtained using InterRAI-PC and scores obtained using MD Anderson Symptom Inventory (MDASI)
Tidsramme: Baseline
InterRAI-PC Scales versus MDASI scales (Pain Scale, dyspnea scale and Depression Rating Scale)
Baseline

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Sensitivity to change: change in InterRAI-PC score over 7 days from Baseline
Tidsramme: One Week
InterRAI-PC scale
One Week
Inter-Observer Reliability of InterRAI-PC scale: correlation between score obtained by different observers (kappa coefficient)
Tidsramme: Baseline
InterRAI-PC scale
Baseline

Samarbejdspartnere og efterforskere

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

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 2013

Primær færdiggørelse (Forventet)

1. september 2016

Studieafslutning (Forventet)

1. juli 2017

Datoer for studieregistrering

Først indsendt

8. januar 2015

Først indsendt, der opfyldte QC-kriterier

17. maj 2016

Først opslået (Skøn)

19. maj 2016

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

19. maj 2016

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

17. maj 2016

Sidst verificeret

1. maj 2016

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 12-002-0105

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 Palliativ pleje

3
Abonner