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Completed

NCT Number: NCT04119570

CKD Report Card Pilot Trial

The investigators will study physician-patient communication at the UCMC nephrology fellow clinic and to test an intervention, the CKD Report Card, to improve that communication and patient knowledge of CKD.

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Key information

Conditions

CKD

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Chicago Medical Center

Chicago, Illinois, 60637, United States

About this study

The goals of the study are to 1) characterize the effectiveness and patient-centeredness of patient-physician interaction during a nephrology clinic visit both with and without use of the CKD Report Card, and 2) to determine which physician and patient characteristics are associated with effective and patient centered communication. There will be block enrollment. For Nephrology physicians who agreed to participate will complete a baseline questionnaire. Research assistants will approach patients of participating providers in clinic waiting rooms, with the goal of enrolling patients for each provider For half of the study, investigators will enroll patients in the study and observe patient-physician communication and use a survey measure CKD knowledge pre-visit and post-visit. For the second half of the study, investigators will give participants the CKD Report Card, an investigator-developed handout, to use during the clinic visit. Investigators will observe patient-physician communication and use a survey to measure CKD knowledge pre-visit and post-visit. For both groups, eligible participants will give informed consent and will complete a baseline questionnaire; research assistants will place a digital audio-recording device in the examination room to record the patient-provider encounter. Following the medical encounter, research assistants will administered an interview with patients, assessing demographic, social, and behavioral characteristics, as well as their experience of care and ratings of provider communication.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • English-speaking adult patients (age 18 or older)
  • Identified in the medical record as non-Hispanic Black or non- Hispanic White
  • seen in University of Chicago nephrology clinic with a participating nephrologist

Exclusion criteria

  • not able to communicate in English
  • lacking ability to consent to study
  • does not identify as non-Hispanic Black or non-Hispanic
  • without chronic kidney disease

Treatment and study plan

CKD Report Card

Behavioral

The CKD Report Card is a handout based on a NKDEP Educational Sheet that includes basic information about kidney disease and spaces where patient can record information about their own kidney disease

Primary outcomes

  1. CKD Knowledge

    Time frame: Change in CKD Knowledge from Baseline (pre-visit) to CKD Knowledge immediately post clinic visit (within 15-100 minutes post-clinic visit)

    Kidney Disease Knowledge Survey (KiKs)

Secondary outcomes

  1. patient-physician interaction

    Time frame: immediately post-nephrology clinic visit (on day of enrollment, within 15-100 minutes post-clinic visit)

    Perceived efficacy in patient-physician interactions (PEPPI)

  2. communication assessment

    Time frame: immediately post-nephrology clinic visit (on day of enrollment, within 15-100 minutes post-clinic visit)

    communication assessment tool (CAT)

Sponsors and collaborators

Lead sponsor

University of Chicago

Other

Registry information

Official study title

Pilot and Trial of the Chronic Kidney Disease Report Card

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Oct 8, 2019
Registry last updated
May 6, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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