Mapping Recovery, Quality of Life, and Physical Function After Partial and Radical Nephrectomy
Aim:
To investigate recovery, quality of life, and physical function before and after partial or radical nephrectomy.
To validate the Quality of Recovery-15 (QoR-15) questionnaire in a urological cohort and investigate whether the questionnaire can be used to identify differences in patient-reported recovery across patient populations.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Antatt)
Kontakter og plasseringer
Studiesteder
-
-
-
Herlev, Danmark, 2730
- Rekruttering
- Department of Urology, Copenhagen University Hospital Herlev and Gentofte
-
Ta kontakt med:
- Marie Juul-Haslund, MD
- Telefonnummer: 004538682699
- E-post: marie.juul-haslund@regionh.dk
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
All patients >18 years scheduled for radical or partial nephrectomy
Beskrivelse
Inclusion criteria
- Scheduled for radical or partial nephrectomy (all surgical approaches).
- Benign or malignant indication for surgery.
- Age >18 years. Exclusion criteria
- Unable to read Danish.
- Unable to complete the questionnaire.
- Emergency surgery.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Observasjonsmodeller: COHORT
- Tidsperspektiver: PROSPECTIVE
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in quality of recovery from enrollment to outpatient follow-up 21 days after surgery
Tidsramme: From enrollment to the end of follow up 21 days after surgery
|
Quality of recovery is evaluated with the danish translation of the verified questionnaire Quality of Recovery-15. It is a 15-item patient questionnaire, where the score ranges from 0-150. A higher score indicates better patient-reported quality of recovery. QoR-15 will be assessed preoperatively, and 1, 2, 7 and 21 days after surgery. Change in QoR-15 from enrollment to 21 days after surgery is the primary outcome measure. Change in QoR-15 at other assessment times will be assessed as secondary outcome measures. |
From enrollment to the end of follow up 21 days after surgery
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Quality of Recovery at other predefined time points.
Tidsramme: Multiple times from enrollment to outpatient follow-up at 21 days after surgery
|
Quality of recovery is measured by the danish translation of the verified questionnaire Quality of Recovery-15. It is a 15-item patient questionnaire, where the score ranges from 0-150. A higher score indicates better patient-reported quality of recovery. QoR-15 will be assessed at preoperatively, and 1, 2, 7 and 21 days after surgery. |
Multiple times from enrollment to outpatient follow-up at 21 days after surgery
|
|
Change in quality of life assessed using the EQ-5D-5L
Tidsramme: From enrollment to the end of follow up 21 days after surgery
|
Quality of life is evaluated with the danish translation of the validated questionnaire EQ-5D-5L. The questionnaire evalutes five health dimensions (mobility, self-care, usual acitivites, pain/discomfort, anxiety/depression) ranging from "no problems" to "unable/ extreme problems". Additionally, it includes a visual analog scale scoring from 0-100, reflecting the participants overall self-reported health state. A higher score indicates a better patient-reported quality of life. Quality of life will be assessed preoperatively and 21 days after surgery. |
From enrollment to the end of follow up 21 days after surgery
|
|
Physical function assessed using the 30 second sit to stand, handgrip strength and 6 minute walking test.
Tidsramme: From enrollment to the end of follow up, 21 days after surgery
|
Physical function assessed using the 30 second sit to stand test (number of repetitions in 30s), handgrip strength test (maximum voluntary muscle strength in kg) and 6 minute walking test (distance in meters). The higher the test results, the better, for all tests. The tests are performed preoperatively and 21 days after surgery. |
From enrollment to the end of follow up, 21 days after surgery
|
|
Validation parameters for the Quality of Recovery-15.
Tidsramme: From enrollment to the end of follow up, 21 days after surgery
|
An evaluation of validity, reliability, responsiveness and feasibility of the Quality of Recovery-15, assessed preoperatively, and 1, 2, 7 and 21 days after surgery. |
From enrollment to the end of follow up, 21 days after surgery
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- F-26022406
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .