Evaluate Serious Illness Treatment Preferences and Outcomes in the Patients Receiving Peritoneal Dialysis
1 other identifier
interventional
500
0 countries
N/A
Brief Summary
The goal of this clinical research study is to study the cardiopulmonary resuscitation (CPR) preferences of patients receiving peritoneal dialysis and how these preferences are associated with their responses to questions about aspects of end-of-life care. This prospective cohort clinical trial aims to provide evidence on the preferences of end of life care in patients receiving peritoneal dialysis, thereby provide optimal care according to patients' preferences and choices through effective communication and clear goals of care.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Feb 2022
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 8, 2021
CompletedFirst Posted
Study publicly available on registry
January 18, 2022
CompletedStudy Start
First participant enrolled
February 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2023
CompletedJanuary 28, 2022
August 1, 2021
Same day
December 8, 2021
January 18, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
the preferences of end of life care in patients receiving peritoneal dialysis
Participants were asked to respond to the questions(POLST questionnaire) associated to life-sustaining treatment preference including CPR preference and other treatment preferences, and life values,
up to 24 weeks
Secondary Outcomes (4)
compare the quality of life after receiving timely integrated palliative care to the other group
3 moths,6 months and 12months after receiving timely integrated palliative care
compare the quality of death after receiving timely integrated palliative care to the other group
3 moths,6 months and 12months after receiving timely integrated palliative care
compare the symptoms burden after receiving timely integrated palliative care to the other group
3 moths,6 months and 12months after receiving timely integrated palliative care
compare the ICU admission frequency after receiving timely integrated palliative care to the other group
3 moths,6 months and 12months after receiving timely integrated palliative care
Study Arms (2)
Refuse to integrate palliative care into usual care.
NO INTERVENTIONUsual ESRD care team
Agree to integrate palliative care into usual care.
EXPERIMENTALUsual ESRD care + combined palliative care team
Interventions
shared decision making with patient, and timely integrated palliative care according to patient's preference
Eligibility Criteria
You may qualify if:
- \[Patients\] Diagnosis of ESRD
- \[Patients\] Under treatment of peritoneal dialysis
- \[Patients\] Age 20 years or older
- \[Caregivers\] Age20 years or older
You may not qualify if:
- \[Patients\] unable to understand or fill in the questionnaire
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Chun-Fu Lai, M.d.
National Taiwan University Hospital
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- SCREENING
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 8, 2021
First Posted
January 18, 2022
Study Start
February 1, 2022
Primary Completion
February 1, 2022
Study Completion
August 31, 2023
Last Updated
January 28, 2022
Record last verified: 2021-08