- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT01914848
Multiprofessional Advance Care Planning and Shared Decision Making for End of Life Care (MAPS)
Multiprofessional Advance Care Planning and Shared Decision-making for End of Life Care MAPS Trial
Multiprofessional Advance Care Planning and shared decision making for end of live care for terminal patients and their relatives.
The aim of this study is to develop, implement and test a complex intervention for improving patients' preparation for and participation in end of life decisions. In cooperation with local, national and international partners, the investigators will focus on strategies to enhance advance care planning and shared decision making on end of life issues, and documentation and transferability of end of life decisions across health care settings in coordinated approach involving patients, their families and care givers (in and out of hospital).
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
ZH
-
Zurich, ZH, Schweiz, 8091
- University Hospital Zurich, Clinical Ethics
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion criteria: -patients in which the treating physician on the ward would not be surprised if the patient died during the next year (surprise question of Weissman et al 2011)
- male and female patients above 18 years of age
- signed informed consent after being informed
- patients able to appoint a surrogate decision maker (SM) and/or responsible physician to be contacted after discharge
Exclusion criteria: -patients not capable of speaking german
- patients having no responsible physician to be contacted after discharge and no relative/future surrogate decision maker (SM)
- inhouse patients being discharged within the next 2 days or ambulatory patients not regularly coming to the wards (at least every two month)
- patients assessed by their physician to be in obvious denial of their situation (illness/prognosis)
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Unterstützende Pflege
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Verdreifachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
---|---|
Aktiver Komparator: Control Group
A routine care discharge planning with the social service
|
A routine care discharge planning with the social service
|
Experimental: Advance Care Planning ACP
Patient get a decision aid video and library and up to 3 consultations with qualified Advance Care Planning Facilitators. -------------------------------------------------------------------------------- |
Patient of the intervention group get a decision aid video and library and up to 3 consultations with qualified Advance Care Planning Facilitators.
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
---|---|
end of life wish on resuscitation known (if alive) or fulfilled(if dead) after 6 month by responsible physician and/or surrogate decision maker (SM)
Zeitfenster: during 2 weeks six months after discharge
|
during 2 weeks six months after discharge
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
---|---|
end of live decisions on last place of care, antibiotics for pneumonia, feeding tube, intravenous fluids, dialysis, intubation and sedation,
Zeitfenster: during 2 weeks six months after discharge
|
during 2 weeks six months after discharge
|
decisional conflict scale ("DCS"), O Connor et al 1995
Zeitfenster: at discharge and during 2 Weeks six months after discharge
|
at discharge and during 2 Weeks six months after discharge
|
Satisfaction with information and care, (see Detering et al 2010)
Zeitfenster: at discharge
|
at discharge
|
Hospital Anxiety and Depression scale ("HADS")
Zeitfenster: discharge and during 2 weeks six months after discharge
|
discharge and during 2 weeks six months after discharge
|
Having an Advance directive
Zeitfenster: at discharge, during 2 weeks three months after discharge and during 2 weeks six months after discharge
|
at discharge, during 2 weeks three months after discharge and during 2 weeks six months after discharge
|
Having an appointed surrogate decision maker
Zeitfenster: at discharge, during 2 weeks three month after discharge and during 2 weeks six month after discharge
|
at discharge, during 2 weeks three month after discharge and during 2 weeks six month after discharge
|
Any hospital stay
Zeitfenster: during 2 weeks three months after discharge and during 2 weeks six months after discharge
|
during 2 weeks three months after discharge and during 2 weeks six months after discharge
|
Decisions regarding end of life issues already having been made/taken place
Zeitfenster: during 2 weeks six months after discharge
|
during 2 weeks six months after discharge
|
open question on important medical decisions being made
Zeitfenster: during 2 weeks three months after discharge
|
during 2 weeks three months after discharge
|
Treatment against patients wishes
Zeitfenster: during 2 weeks three months after discharge and during 2 weeks six months after discharge, or 3 month after death
|
during 2 weeks three months after discharge and during 2 weeks six months after discharge, or 3 month after death
|
Distress of Patients or relatives because of content of the consultation
Zeitfenster: at discharge, during 2 weeks three months after discharge and during 2 weeks six months after discharge
|
at discharge, during 2 weeks three months after discharge and during 2 weeks six months after discharge
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Tanja Krones, MD, University Hospital Zurich, Clinical Ethics
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Schätzen)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- MAPS Trial
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Palliativpatienten
-
Indonesia UniversityAbgeschlossen
-
University Health Network, TorontoAktiv, nicht rekrutierendFortgeschrittener Krebs | Immuntherapie | Strahlentherapie | PalliativKanada
-
Vrije Universiteit BrusselUnbekanntPalliativ | Lebensbedrohliche Krankheit
-
Hospital do CoracaoMinistry of Health, Brazil; Fisher and Paykel HealthcareBeendetAtemstillstand | Pflege, PalliativBrasilien
-
University Health Network, TorontoRekrutierung
-
Peking Union Medical College HospitalAbgeschlossenPatient nach Herzklappenoperation | Patient mit verlängerter mechanischer BeatmungChina
-
Centre Hospitalier Universitaire de NiceAbgeschlossenVorherrschender Alzheimer-Patient | Demenzieller Alzheimer-Patient | ZeugeFrankreich
-
Vanderbilt University Medical CenterAbgeschlossenBildung, Medizin | Pflege, Palliativ | Bildung, Medizin, Absolvent | Medizin, PalliativmedizinVereinigte Staaten
-
Fondazione Policlinico Universitario Agostino Gemelli...Noch keine RekrutierungHerzchirurgischer Patient
-
University of Mississippi Medical CenterNational Center for Complementary and Integrative Health (NCCIH); University...AbgeschlossenAdhärenz, PatientVereinigte Staaten
Klinische Studien zur Control Group
-
Acibadem UniversityAbgeschlossenPfleger-Patienten-BeziehungenTruthahn
-
Columbia UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development...AbgeschlossenSchlafen | Asthma | Asthma bei KindernVereinigte Staaten
-
U.S. Army Medical Research and Development CommandUnited States Agency for International Development (USAID); University of Oxford und andere MitarbeiterAbgeschlossen
-
Hui-Hsun ChiangAbgeschlossenErziehungsprobleme | Pflege | Gewalt am ArbeitsplatzTaiwan
-
Indiana UniversityEunice Kennedy Shriver National Institute of Child Health and Human Development...RekrutierungEmpfängnisverhütung | Nutzung des Gesundheitswesens | Verwendung von VerhütungsmittelnVereinigte Staaten
-
University of Illinois at ChicagoPatient-Centered Outcomes Research Institute; University of ChicagoRekrutierungSchwangerschaftskomplikationen | Patientenbindung | Muster der mütterlichen FürsorgeVereinigte Staaten
-
University of LisbonAssociacao Protectora dos Diabeticos de PortugalAbgeschlossen
-
Universidade Federal de Santa MariaRekrutierungParodontitis | Parodontale Erkrankungen | Motivierende GesprächsführungBrasilien
-
Universitat Jaume IAbgeschlossenDepression | AngststörungenSpanien
-
The Policy & Research GroupMathematica Policy Research, Inc.; The Office of Adolescent Health, HHSAbgeschlossen