A Survey for Patients and Caregivers Aiming to Understand and Improve the Care of Patients at High Risk of Transfer From Peritoneal Dialysis to Hemodialysis:

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCiusss de L'Est de l'Île de Montréal

About this trial

Home dialysis is encouraged in Canada and peritoneal dialysis is the most common home dialysis method. However, many patients discontinue peritoneal dialysis, often transferring to hemodialysis. Despite the frequency of this transition, little is known about its impact on patients.

Overall, the UPLIFT-PD program aims to fill this gap by studying the transition from peritoneal dialysis to hemodialysis. The specific goal of this mixed methods sub-study is to conduct a national survey to ask patients and caregivers about priorities and preferences when they anticipate a transfer from peritoneal dialysis to hemodialysis. This survey will be co-created by patient-partners and dialysis experts.

Results from this survey will then be used in other phases of UPLIFT-PD program, detailed in other registrations, which will support people facing a transition from peritoneal dialysis to hemodialysis..

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adult (≥18 years)

Patient who experienced a PD-to-HD transition in past 12 months

Patient currently receiving peritoneal dialysis

Caregiver (self-defined, including spouses, family members, or friends) of individuals meeting the above criteria

Disqualifiers

Age <18 years

Unable to provide consent

Trial population

Adult patients with lived experience of peritoneal dialysis and transitions to hemodialysis, as well as caregivers of such patients, recruited from dialysis centers and patient communities across multiple centers.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

200 Participants
are grouped into 1 trial group
Group A: Survey Participants

Trial outcomes

Primary outcomes

1

Priorities and Challenges Related to PD-to-HD Transitions

Measured using Likert-scale responses assessing perceived importance of transition-related factors (e.g. preparedness, timing of discussions, vascular access planning, psychosocial impact). Likert-scale from 0 (lowest importance) to 9 (highest importance)

Time frame
At survey completion (Baseline)

Secondary outcomes

1

Preferences for Clinical Scenarios Related to PD-to-HD Transitions

Assessed using a discrete choice experiment evaluating trade-offs between attributes such as duration on PD, risk of complications, and planned vs. unplanned HD transfer.

Time frame
At survey completion (Baseline)
2

Perceptions of Successful Transition

Agreement with proposed definitions of successful PD-to-HD transitions based on care pathways.

Time frame
At survey completion (Baseline)

Other outcomes

1

Qualitative Themes Related to Transition Experiences

Analysis of open-ended responses to identity key themes and concepts.

Time frame
At survey completion (Baseline)

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ciusss de L'Est de l'Île de Montréal

Lead sponsor

Canadian Institutes of Health Research (CIHR)

Collaborator

This trial is not recruiting at the moment. You can still explore other options: