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Effectiveness of an APN-led Self-management Program in Patients in the First Year After Renal Transplantation (SMP-NEP)

30. april 2021 oppdatert av: University of Zurich

Effectiveness of an Advanced Practice Nurse-led Self-management Program on Prevention of Weight Gain, Physical Activity and Medication Adherence in Patients in the First Year After Renal Transplantation

The aim of this study is to investigate the effectiveness of the program in patients after renal transplantation using a randomized controlled trial design. Physical, behavioural, and clinical outcomes will be measured at baseline before randomization then 8 and 12 months later.

Studieoversikt

Detaljert beskrivelse

Renal transplant recipients have to integrate preventive behaviours into their everyday lives. From the literature it is known that patients can only partially adhere to the recommended behaviours. An evidence-based self-management program to support patients in behaviour change was developed with a main focus on prevention of weight gain and increasing physical activity and medication adherence.

The aim of this study is to investigate the effectiveness of the program in patients in the first year after renal transplantation.

The specific aims of this study are:

  1. Compare differences in weight gain between subjects in the IG (intervention group) and in the CG (control group).
  2. Compare differences in the amount of physical exercise between subjects in the IG group and the CG.
  3. Compare differences in self-reported medication adherence between the subjects of the IG group and the CG.

Secondarily, differences in self-reported quality of life, anxiety and depression, and differences in patients' perception of health care provision regarding chronic illness between the subjects of the IG group and the CG will be compared.

Design: Randomised controlled trial, not blinded

Setting and time: The study will take place at the Nephrology Clinic, University Hospital Zürich, from 1 May 2012 through 31 April 2015.

Variables and Measurement: Physical, behavioural, and clinical outcomes will be measured at baseline, before randomization and then 8 and 12 months later. Medication adherence, physical activity, symptoms of depression and anxiety, quality of life and patients' perception of health care provided will be measured with validated questionnaires. Body weight, height, waist to hip ratio and body composition (BCM Fresenius) will be measured at the Nephrology Clinic. Physical activity will be measured with the pedometer StepWatchTM.

Intervention

Studietype

Intervensjonell

Registrering (Faktiske)

122

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

      • Zurich, Sveits, 8091
        • University Hospital Zurich

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • received a kidney or a kidney-pancreas transplant in the University Hospital Zürich

Exclusion Criteria:

  • unstable psychiatric disorder
  • cognitive impairment
  • multi-organ transplantation with lung
  • liver or heart
  • illiteracy
  • not able to speak and understand German

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Annen: Styre
Session takes place within the first three months after transplantation
Eksperimentell: Intervention

The intensity of the intervention follows a defined algorithm during the first eight months after renal transplantation. Behaviours are classified in three groups:

  • Group 1: Patients with optimal behaviour in all three behaviours.
  • Group 2: Patients with slight deviation (defined) from optimal behaviour in one or more behaviours.
  • Group 3: Patients with larger deviation (defined) from optimal behaviour in one or more behaviours.

All patients (group 1-3) will receive an assessment, education and a monthly reassessment.

Patients from group 2 und 3 will receive additionally behavioral education and peer involvement. Patients from group 3 will receive additionally a consilium of specialized healthcare professionals such as a nutritionist, physiotherapist, or psychologist.

Patients participate in 9 sessions during the first 8th month after transplantaiton

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
change from baseline BMI at 8 months
Tidsramme: 8th month
BMI
8th month

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
difference of activity between control and intervention group at month 8
Tidsramme: month 8
differences in steps measured with pedometer (Stepwatch)
month 8
difference of activity between control and intervention group at month 12
Tidsramme: month 12
differences in steps measured with pedometer (Stepwatch)
month 12
change from baseline BMI at 12 months
Tidsramme: 12th month
BMI
12th month
difference of self-reported adherence between control and intervention group at month 8
Tidsramme: month 8
month 8
difference of self-reported adherence between control and intervention group at month 12
Tidsramme: month 12
month 12
change from baseline LTM at 8 months
Tidsramme: 8 months
LTM measured with Body Composition Analysis
8 months
change from baseline LTM at 12 months
Tidsramme: 12 months
LTM measured with Body Composition Analysis
12 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Rebecca Spirig, PHD, RN, Nursing Director, Head Office of Nursing and Allied Health Professionals

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

1. mai 2012

Primær fullføring (Faktiske)

1. januar 2018

Studiet fullført (Faktiske)

1. februar 2018

Datoer for studieregistrering

Først innsendt

27. oktober 2014

Først innsendt som oppfylte QC-kriteriene

3. november 2014

Først lagt ut (Anslag)

4. november 2014

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

3. mai 2021

Siste oppdatering sendt inn som oppfylte QC-kriteriene

30. april 2021

Sist bekreftet

1. april 2021

Mer informasjon

Begreper knyttet til denne studien

Nøkkelord

Andre studie-ID-numre

  • KEK-ZK-Nr. 2011-0411

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. .

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