Frequently Asked Questions for ICU Patients' Families (FamiréaXVII)
Frequently Asked Questions as an Help to Improve the Information of ICU Patients' Families.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
Half of the families of ICU patients do not understand the information provided by doctors and nurses. Receiving clear, loyal and appropriate information is one of their main expectations. We have previously reported that relatives had difficulty asking questions that allow them to improve their understanding regarding ICU issues. In a preliminary study, we developed a list of questions considered as important by families, ICU doctors and nurses.
The aim of this prospective, randomized and controlled trial is to test the effectiveness of a list of frequently asked questions to relatives of ICU patients on their understanding of the provided information.
The intervention consists of the delivery of a list of 21 questions to the relative of each patient admitted in intensive care, intubated and mechanically ventilated in the first 48 hours of ICU stay. A formal interview is scheduled for relatives at Day 3 of inclusion. The information comprehension at Day 5 (± 1) will be compared between families that received the list of "FAQ" and families that received information as usual (without providing the list of FAQ).
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
-
-
-
Marseille, Frankrig, 13354
- Hôpital Nord Assistance Publique Hôpitaux de Marseille
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
The subjects that will be included are relatives of patients. The patients must be
- Adults
- Receiving invasive mechanical ventilation
- Intubated in the first 48 hours of ICU admission
- For an expected duration of mechanical ventilation > 48 hours
- With a life expectancy of at least 5 days and a SAPS 2 at baseline < 75
- Who received a visit within 24 hours after intubation. Only one relative will be included.
Exclusion Criteria:
- person unable to read French
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Kohorter og interventioner
Gruppe / kohorte |
Intervention / Behandling |
|---|---|
|
families that received the list of "FAQ"
The intervention consists of the delivery to the relatives of ICU patients a list of "21 key issues" in intensive care during the first 48h period of ICU stay, only for intubated and mechanically ventilated patients A formal interview is scheduled to relatives of ICU patients on D3 of inclusion
|
|
|
families that received information as usual
A formal interview is scheduled relatives of ICU patients on D3 inclusion
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Evaluation of understanding at day 5 by a method of reformulation questionnaire
Tidsramme: 5th day after inclusion
|
The physician in charge of the patient provides the diagnosis, the treatment and the prognosis to the investigator prior to meet the relative. After the meeting, the relative gives to the investigator the diagnosis, main treatements and the prognosis as they have undestood them. In a final step, the investigator will indicate whether similar responses are consistent or not consistent. |
5th day after inclusion
|
|
Scale of satisfaction out of intensive care.
Tidsramme: 3 months and at one yearfter inclusion
|
HADS scores and IES-R at day 5 to day 10.
|
3 months and at one yearfter inclusion
|
Samarbejdspartnere og efterforskere
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart
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 (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- RC12_3678
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 list of "FAQ"
-
Institute for the Study of Urological Diseases,...Ikke rekrutterer endnuErektil dysfunktion
-
University of Wisconsin, MadisonPatient-Centered Outcomes Research Institute; Brigham and Women's Hospital og andre samarbejdspartnereAfsluttet
-
Stanford UniversityNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Ikke rekrutterer endnuGastroøsofageal refluks | Patient aktiveringForenede Stater
-
Institute for the Study of Urological Diseases,...RekrutteringErektil dysfunktionGrækenland
-
Institute for the Study of Urological Diseases,...AfsluttetErektil dysfunktion | Lav intensitet stødbølgeterapiGrækenland
-
Virginia Commonwealth UniversityAfsluttetOndartet neoplasma | Leukæmi, ikke andet angivetForenede Stater
-
Johns Hopkins UniversityNational Institute on Aging (NIA)Aktiv, ikke rekrutterendeAlzheimers sygdom, tidligt debut | Logopenisk progressiv afasi | Atypisk Alzheimers sygdomForenede Stater
-
University Hospital, Clermont-FerrandUkendt
-
Maastricht UniversityTNO; Netherlands Instititute for Health Services Research; University of...AfsluttetHjertefejl | Diabetes mellitus, type 2 | Kronisk obstruktiv lungesygdom | AstmaHolland
-
New York State Psychiatric InstituteUniversity of Miami; Columbia University; University of Southern California; Feinstein Institute for Medical ResearchSuspenderetSunde deltagereForenede Stater