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Information Sharing for Chronic Kidney Disease
Study Summary
This trial will test whether providing patients with information about their risk of kidney failure improves quality of care, health literacy, and trust in the care they are receiving.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
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- I have chronic kidney disease between stages 3 to 5.Criterion: Healthcare clinics in Manitoba and Alberta that care for adults in the community and use a specific electronic medical record system to help manage and refer patients with chronic kidney disease.
- Group 1: Active Knowledge Translation Group
- Group 2: Control Group
- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
Are there any openings for individuals to join this experiment?
"The clinical trial is actively seeking volunteers; the initial posting was made on August 24th 2018, with a recent update seen on June 9th 2022."
What is the scope of enrollees for this experiment?
"Affirmative. According to clinicaltrials.gov, this trial is recruiting and was posted on August 24th 2018 with the latest edit occuring June 9th 2022. Approximately 6300 participants are sought from two separate medical facilities."
What objectives is this experiment seeking to accomplish?
"The principal outcome of this trial, to be evaluated within a year after the intervention, is the proportion of patients who are being treated adequately with ACEi or ARB and have either CKD and diabetes, or CKD plus urine ACR >30 mg/mmol. Subsidiary objectives include assessing clinical providers' satisfaction with risk prediction tools & decision aids (measured by Likert scale points), monitoring cardiovascular risk factors for CKD patients (proportion w/ statin prescription in EMR) & evaluating patient's kidney-related health literacy (number of KiKS survey answers)."
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