Experiences and Health-related Quality of Life of Informal Caregivers of Dialysis Patients

NCT05646615 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 202

Last updated 2024-12-12

No results posted yet for this study

Summary

The goal of this prospective, observational, multicentre cohort study is to assess the trajectory of the experiences (both positive and negative) and health-related quality of life (HRQOL) of informal caregivers of patients who start home dialysis, and compare these to experiences and HRQOL of informal caregivers of patients who start in-centre hemodialysis. The investigators hypothesise that informal caregivers of home dialysis patients experience more positive experiences, but also more negative experiences, and still have better HRQoL, compared with caregivers of in-centre HD patients. Participants will fill in five different validated questionnaires and questions on required support. Participants are asked to fill in the questionnaires after inclusion (i.e., start of dialysis), and at 6 and 12 months after start dialysis.

Conditions

  • Peritoneal Dialysis
  • Hemodialysis, Home
  • Hemodialysis
  • Quality of Life
  • Informal Caregivers
  • Family Caregivers
  • Renal Replacement Therapy
  • Kidney Failure, Chronic
  • Patient Reported Outcome Measures

Sponsors & Collaborators

  • Admiraal de Ruyter Hospital

    collaborator OTHER
  • Alrijne Hospital

    collaborator OTHER
  • Amphia Hospital

    collaborator OTHER
  • St. Antonius Hospital

    collaborator OTHER
  • Canisius-Wilhelmina Hospital

    collaborator OTHER
  • Catharina Ziekenhuis Eindhoven

    collaborator OTHER
  • Deventer Ziekenhuis

    collaborator OTHER
  • Dialysis Center Beverwijk

    collaborator UNKNOWN
  • Tergooi Hospital

    collaborator OTHER
  • Diapriva Dialysis Center, Amsterdam

    collaborator OTHER
  • Elkerliek Hospital

    collaborator OTHER
  • Flevoziekenhuis

    collaborator OTHER
  • Gelre Hospitals

    collaborator OTHER
  • Groene Hart Ziekenhuis

    collaborator OTHER
  • Haga Hospital

    collaborator OTHER
  • Isala

    collaborator OTHER
  • Laurentius Hospital

    collaborator UNKNOWN
  • Maasstad Hospital

    collaborator OTHER
  • Maxima Medical Center

    collaborator OTHER
  • Noordwest Ziekenhuisgroep

    collaborator OTHER
  • OLVG Oost

    collaborator UNKNOWN
  • OLVG West

    collaborator UNKNOWN
  • Radboud University Medical Center

    collaborator OTHER
  • Reinier de Graaf Groep

    collaborator OTHER
  • Rijnstate Hospital

    collaborator OTHER
  • Saxenburgh Group

    collaborator UNKNOWN
  • Slingeland Hospital

    collaborator OTHER
  • UMC Utrecht

    collaborator OTHER
  • VieCuri Medical Centre

    collaborator OTHER
  • Amsterdam UMC

    collaborator OTHER
  • Bernhoven Hospital

    collaborator OTHER
  • ZorgSaam

    collaborator UNKNOWN
  • Jessa Hospital

    collaborator OTHER
  • B.C. van Jaarsveld

    lead OTHER

Principal Investigators

  • Brigit C van Jaarsveld, MD, PhD · Amsterdam UMC, location VUmc

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2023-12-31
Completion
2023-12-31

Countries

  • Belgium
  • Netherlands

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05646615 on ClinicalTrials.gov