No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
70 (estimated)
Sponsor
Massachusetts General Hospital · Other
Who this trial is looking for
This trial is looking for adults with advanced chronic kidney disease (CKD) to participate in regular symptom reporting with feedback from their doctors. Participants will help improve understanding and treatment of their symptoms.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old.
I have advanced chronic kidney disease.
I have two recent tests showing low kidney function.
I can provide consent to join the study.
I can read and write in English.
I see a nephrologist at a Mass General Brigham clinic.
You may not be able to join if
I have a terminal illness likely to lead to death in the next 6 months.
I am currently receiving dialysis treatment.
I am scheduled to start dialysis in the next 4 weeks.
I am scheduled to receive a kidney transplant in the next 6 months.
I am new to the nephrology clinic.
I have cognitive deficits that hinder my understanding of consent or questionnaires.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Patient-reported outcome measures (PROMs) are validated tools to reliably measure outcomes highly prioritized by patients, such as health-related quality of life (HRQOL) and symptoms, but the current clinical impact of PROMs is limited by a lack of evidence-based methods to incorporate them into routine care. Symptoms, which are highly prevalent among persons living with chronic kidney disease (CK…
Patient-reported outcome measures (PROMs) are validated tools to reliably measure outcomes highly prioritized by patients, such as health-related quality of life (HRQOL) and symptoms, but the current clinical impact of PROMs is limited by a lack of evidence-based methods to incorporate them into routine care. Symptoms, which are highly prevalent among persons living with chronic kidney disease (CKD), substantially contribute to the reduced HRQOL experienced by this patient population. HRQOL spans several domains of wellbeing affected by disease, including physical, mental, and social health, functionality, and symptoms. Both HRQOL and symptom burden are consistently identified by patients with CKD as top clinical and research priorities. These issues are particularly salient to individuals living with advanced CKD, who suffer significant symptom burden that is often underrecognized and undertreated by nephrology providers, yet is a key factor considered by nephrologists for the timing of dialysis initiation. Randomized controlled trials of patients with other chronic illnesses show that routine assessment of symptoms with PROMs improves symptom burden, patient-provider communication, and HRQOL; yet, standardized approaches to regular symptom monitoring among patients with advanced CKD are lacking. This pilot, randomized trial of a PROM-based intervention for routine symptom reporting by patients with feedback of responses to nephrologists aims to address the lack of data on PROM use for symptom assessment in nephrology care. We will evaluate the implementation (reach, feasibility, and acceptability) and preliminary efficacy of monthly patient report of CKD-related symptoms using the electronic IPOS-Renal questionnaire with supported clinician follow-up for 12 months versus standard of care. This trial will utilize complementary quantitative and qualitative methods to evaluate the implementation of the PROM-based intervention. The results of this pilot study will inform a definitive, cluster-randomized trial on the effect of a PROM-based symptom assessment intervention to improve HRQOL and clinical outcomes among patients living with advanced CKD.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Adults (age ≥ 18 years)
* Advanced CKD, defined as at least two measurements of creatinine-based or cystatin C-based eGFR ≤ 30 mL/min/1.73m2 separated by at least 90 days in the preceding 12 months
* Able to provide consent to participate in the study
* Able to read and write …
Inclusion Criteria:
* Adults (age ≥ 18 years)
* Advanced CKD, defined as at least two measurements of creatinine-based or cystatin C-based eGFR ≤ 30 mL/min/1.73m2 separated by at least 90 days in the preceding 12 months
* Able to provide consent to participate in the study
* Able to read and write in English
* Under the care of a nephrologist at a Mass General Brigham nephrology clinic
Exclusion Criteria:
* Terminal illness likely to lead to death within 6 months of participation
* Patients receiving dialysis treatment at the time of enrollment or scheduled to start dialysis therapy in the next 4 weeks
* Patients scheduled to receive a kidney transplant in the next 6 months
* Patients having their initial clinic visit (i.e., new to the clinic)
* Cognitive deficits that would preclude understanding of consent form and/or questionnaires
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