- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02824783
Quality of Life After Enhanced Recovery Protocol for Colorectal Surgery
Quality of Life and Satisfaction of Patients Discharged Home After Enhanced Recovery Protocol for Colorectal Surgery
The aim of the study is to investigate the quality of life and satisfaction of patient who underwent colorectal surgery using an enhanced recovery protocol when back home.
In this retrospective study patients will be telephoned and asked to answer a questionnaire.
Studieoversigt
Status
Betingelser
Detaljeret beskrivelse
Since October 1st 2015, our center has been labelled reference center for colorectal surgery using Enhanced Recovery Protocol (ERP) by GRACE (Groupe francophone de Rehabilitation après ChirurgiE; a francophone counterpart of ERAS® society). In case of ERP, the quality of life when the patient is at home is not well known. Some argue that patient might experience discomfort and lack of autonomy, particularly elderly patient if discharged home too quickly.
In this study, the investigators will call our patients introduced in the database of GRACE to assess the quality of life and patient satisfaction concerning our ERP. Eight domains will be investigated: information, stress, feelings when discharged home, pain, fatigue, autonomy, feeding problems, and satisfaction.
When analyzing the results the investigators will pay a particular attention to elderly patients (age > 70 yo) to determine whether these experience more difficulties as compared to younger patients.
Undersøgelsestype
Tilmelding (Faktiske)
Kontakter og lokationer
Studiesteder
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Liege, Belgien, 4000
- University Hospital of Liege
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Barn
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Prøveudtagningsmetode
Studiebefolkning
Beskrivelse
Inclusion Criteria:
- all patients included in our GRACE database
Exclusion Criteria:
- No exclusion criteria
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Quality of life (0 to ten numeric scale + questionnaire)
Tidsramme: first month after leaving the hospital
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0 to ten numeric scale + questionnaire
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first month after leaving the hospital
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Satisfaction (0 to ten numeric scale + questionnaire)
Tidsramme: first month after leaving the hospital
|
0 to ten numeric scale + questionnaire
|
first month after leaving the hospital
|
|
Pain (0 to ten numeric scale + questionnaire)
Tidsramme: first month after leaving the hospital
|
0 to ten numeric scale + questionnaire
|
first month after leaving the hospital
|
|
Fatigue (0 to ten numeric scale + questionnaire)
Tidsramme: first month after leaving the hospital
|
0 to ten numeric scale + questionnaire
|
first month after leaving the hospital
|
Samarbejdspartnere og efterforskere
Sponsor
Efterforskere
- Ledende efterforsker: Jean Joris, M.D., Department of Anesthesiology, CHU Liege, Belgium
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 (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
- GRACE1
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
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