- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT03612934
The Impact of SPC on Advanced Breast Cancer Patients
26. juli 2018 opdateret af: Łukasz Pietrzyński, Silesian University of Medicine
The Influence of Specialist Palliative Care on the Exacerbation of Negative Symptoms, Life Quality and Performance Status of Patients With Advanced Breast Cancer
The aim of this prospective, observational study is the evaluation of the effectiveness of a 14-day Specialist Palliative Care therapy in participants with advanced breast cancer carried out in a stationary palliative care unit in Poland.
The length of the entire study will be 36 months.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Undersøgelsestype
Observationel
Tilmelding (Faktiske)
144
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
33 år til 91 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Kvinde
Prøveudtagningsmetode
Ikke-sandsynlighedsprøve
Studiebefolkning
Patients with advanced stage breast cancer refered for a SPC treatment at palliative care department in Poland, Będzin.
Beskrivelse
Inclusion Criteria:
the patient's conscious consent for examination and the ability to fill in the form by the patient herself.
-
Exclusion Criteria:
- patients with cognitive disturbances disabling credible answers in the questionnaire, deceased patients or those discharged from the ward before 14 days of hospitalisation.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
patients under the age of 65 years
|
In the research, Specialist Palliative Care was provided according to the guidelines established by Mid-Western Health Board in a Report of the National Advisory Committee on Palliative Care as well as according to recommendations of Polish Society of Palliative Medicine and Polish National Healthcare Fund.
In order to ensure interdisciplinary and integrated palliative care, a team of specialists was appointed.
Team members were engaged in the process of treatment of each patient during the time of the study and applied their specialist skills according to the needs of the patients
|
|
patients at the age of 65 years and over
|
In the research, Specialist Palliative Care was provided according to the guidelines established by Mid-Western Health Board in a Report of the National Advisory Committee on Palliative Care as well as according to recommendations of Polish Society of Palliative Medicine and Polish National Healthcare Fund.
In order to ensure interdisciplinary and integrated palliative care, a team of specialists was appointed.
Team members were engaged in the process of treatment of each patient during the time of the study and applied their specialist skills according to the needs of the patients
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Variation of intensification of patients negative symptoms before and after SPC
Tidsramme: 14 days
|
intensification of patients negative symptoms was assessed by Edmonton Symptom Assessment System (esas)
|
14 days
|
|
Variation of performance status of patients before and after SPC
Tidsramme: 14 days
|
performance status of patients was assessed by ECOG scale (Eastern Cooperative Oncology Group)
|
14 days
|
|
Variation of quality of life of patients before and after SPC
Tidsramme: 14 days
|
quality of life of patients of patients was assessed by quality of life uniscale (QoLU)
|
14 days
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Studiestol: Jadwiga Jośko-Ochojska, prof, 4. Chair and Department of Medicine and Environmental Epidemiology Medical University of Silesia in Katowice
- Ledende efterforsker: Łukasz Pietrzyńsi, 1. Medical University of Silesia, department of palliative medicine
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)
1. maj 2015
Primær færdiggørelse (Faktiske)
1. maj 2018
Studieafslutning (Faktiske)
1. maj 2018
Datoer for studieregistrering
Først indsendt
9. juli 2018
Først indsendt, der opfyldte QC-kriterier
26. juli 2018
Først opslået (Faktiske)
2. august 2018
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
2. august 2018
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
26. juli 2018
Sidst verificeret
1. juli 2018
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- SPC1
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
UBESLUTET
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