Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06274710

ODYSSEE Kidney Health Trial

Led by University Health Network, Toronto · Updated on 2024-12-12

344

Participants Needed

1

Research Sites

121 weeks

Total Duration

On this page

Sponsors

U

University Health Network, Toronto

Lead Sponsor

S

Sunnybrook Health Sciences Centre

Collaborating Sponsor

AI-Summary

What this Trial Is About

INTRODUCTION Severe CKD is defined as a risk of greater than 10% for progressing to RRT \[home hemodialysis (HHD), home peritoneal dialysis (HPD), and transplantation\] within 2 years. There is a need to improve access to CKD self-care counselling and RRT education for patients with severe CKD. Trials of CKD self-care education have achieved therapeutic benefits with moderate to high patient-provider contact. There is high potential for a trial of digital counselling for CKD self-care and RRT education to enhance patient health and quality of life. HYPOTHESES The primary hypothesis is that ODYSSEE-KH versus usual care (UC) will significantly increase the incidence of home RRT, measured by a composite index of HHD, HPD, and preemptive kidney transplant at trial completion (median = 19 months; range: 12 to 27 months). The secondary hypothesis is that ODYSSEE-KH for CKD self-care and RRT education improves Home RRT, RRT preparation, annual hospitalization rate, engagement with CKD self-care resources at months 6 and 12 and trial completion and scores on outcome measures. RECRUITMENT Patients diagnosed with CKD who are 18 years of age or older were recruited from University Health Network (UHN), Sunnybrook Hospital, Scarborough Health Network, and The Ottawa Hospital. DESIGN ODYSSEE-KH is a double-arm, parallel-group, randomized controlled trial that has assessments at baseline, months 6 and 12, and trial completion (median = 19 months; range: 12 to 27 months). This is a single-blind design with research personnel masked. ODYSSEE-KH combines automated digital counselling of CKD self-care with renal replacement therapy (RRT) education. UC enhances the standard of usual care by providing patients with conventional digital CKD education. Over 27 months, patients will be emailed on a weekly basis with a digital link to log on to their respective program using a password-protected, personal account. ANALYSIS Separate GLMs will evaluate if Digital Counselling versus UC is independently associated with outcomes at months 6 and 12 and trial completion (median = 19; range: 12 to 27 months). Dependent variables include the KDQOL-SF, SF-36, EUROIA, PHQ-9, GAD-7, MIDLS, ESSI, PWB, BMPN, AI, as well as a modified SEMCD-6. Multivariable models will adjust for baseline assessments of each outcome and potential baseline covariates (noted above). In all GLMs, significant interactions will be followed by subgroup analyses with Bonferroni post hoc tests.

CONDITIONS

Official Title

ODYSSEE Kidney Health Trial

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • CKD patients aged 18 years or older with a greater than 10% risk of needing dialysis within 2 years
  • Registered in a nephrology clinic at a participating hospital
  • Stable CKD confirmed by a nephrologist for at least 1 month before enrollment
  • Can understand spoken and written English or French
  • Provided informed written consent
  • At least basic computer literacy
  • Access to the internet and a computer
Not Eligible

You will not qualify if you...

  • Previous kidney transplant or currently waitlisted for an organ transplant
  • Severe health conditions that prevent full participation, such as dementia or severe depression
  • Diagnosed with a medical condition with life expectancy less than 2 years

AI-Screening

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Trial Site Locations

Total: 1 location

1

University Health Network

Toronto, Ontario, Canada, M2N 7A2

Actively Recruiting

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Research Team

R

Robert Nolan, PhD

CONTACT

J

Janice Montbriand, Phd

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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