EPIK: Multi-disciplinary Participatory Design of a Process to Deliver a CKD Diagnosis in Primary Care

Sponsor
University of Michigan (Other)
Overall Status
Completed
CT.gov ID
NCT03084159
Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (NIH)
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Study Details

Study Description

Brief Summary

This study will use an adapted education worksheet to support patient-centered chronic kidney disease (CKD) communication, shared decision making, and patient engagement and will test its impact on intermediate patient modifiable characteristics in a primary care practice with patients who have pre-dialysis CKD.

The study team will enroll up to 100 patients with chronic kidney disease (CKD) from a primary care clinic to start. Patients will receive the intervention, which consists of the physicians using the education worksheet during appointments with patients, and patients and providers will complete surveys about its use and to measure impact on knowledge and other areas related to patient outcomes.

Once initial user testing is complete, the study team plans to submit an amendment to expand on this trial and incorporate comparison sites. This will be submitted and receive IRB approval prior to participant involvement.

The study hypothesis is that patients who receive the intervention will have greater knowledge about their CKD diagnosis, higher satisfaction with provider communication, and higher scores related to managing CKD to keep themselves healthy compared to control populations.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Education worksheet
N/A

Detailed Description

Amendment on 12/2018: The enrollment numbers were updated to include the control group.

Clarification 9/2021: After initial feasibility was assessed, the initial site was used additionally to enroll for the "second arm", rather than a new site as originally intended. A second site was then used for the control population.

Study Design

Study Type:
Interventional
Actual Enrollment :
78 participants
Allocation:
Non-Randomized
Intervention Model:
Factorial Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Multi-disciplinary Participatory Design of a Process to Deliver a CKD Diagnosis in Primary Care
Actual Study Start Date :
Jun 5, 2017
Actual Primary Completion Date :
Sep 11, 2020
Actual Study Completion Date :
Sep 11, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Participatory design and intervention

Patients in this arm will receive the intervention of using an education worksheet during their appointment with their provider. They will be asked to complete post intervention surveys (for feasibility and feedback prior to actual trial enrollment). Providers and staff at this site have been involved in the design of the intervention process, to make it streamlined and efficient for application in practice.

Behavioral: Education worksheet
Patients who screen positive for CKD and give written informed consent to be a part of the study will have their chart flagged for the medical assistant and provider to give the education worksheet intervention. The education worksheet has been developed to be used as an electronic tool within the Electronic Medical Record. The provider will review it with the patient during the visit. A paper copy will print out for the patient at the end of the visit.
Other Names:
  • Education Activation Worksheet
  • Experimental: Intervention Only

    This arm include new patients at the initial site that also received the intervention of using an education worksheet during their appointment and filled out post intervention surveys. Some of these providers/staff were not involved in the initial design of the intervention.

    Behavioral: Education worksheet
    Patients who screen positive for CKD and give written informed consent to be a part of the study will have their chart flagged for the medical assistant and provider to give the education worksheet intervention. The education worksheet has been developed to be used as an electronic tool within the Electronic Medical Record. The provider will review it with the patient during the visit. A paper copy will print out for the patient at the end of the visit.
    Other Names:
  • Education Activation Worksheet
  • No Intervention: Usual Care

    A second site included usual care, which did not include the intervention. Participants were given post visit surveys similar to those in the two other study / intervention arms. This site served as a usual care comparison.

    Outcome Measures

    Primary Outcome Measures

    1. Level of objective understanding of CKD as measured by the Kidney Knowledge Survey (KiKS) [Length of doctor's appointment, e.g., 1-2 hours]

      This will measure objective kidney disease knowledge, based on a score of 0-100, where 0 means poor level of kidney knowledge, and 100 means good level of kidney knowledge. The KiKS was developed by Dr. Wright.

    2. Level of perceived understanding of CKD as measured by the Perceived Kidney Knowledge Survey (PiKS) [Length of doctor's appointment, e.g., 1-2 hours]

      This will measure subjective kidney knowledge. Score range is 1-4, where 1 is low level of perceived kidney knowledge, and 4 is high level of perceived kidney knowledge. The PiKS was developed by Dr. Wright.

    Secondary Outcome Measures

    1. Level of positive perception of patient-provider communication as measured by the Patient Communication Assessment Tool (CAT) [Length of doctor's appointment, e.g., 1-2 hours]

      This assesses the quality of physician to patient and physician's staff to patient communication. Score range is 1-5, where 1 means negative perception of communication and 5 means positive perception of communication.

    2. Level of mental anxiety/stress related to condition as measured by the adapted NDBCSS scale [Length of doctor's appointment, e.g., 1-2 hours]

      The 19-item NDBCSS (Newly Diagnosed Breast Cancer Stress Scale) is adapted to form the 21-item scale in the patient survey to measure stress associated with CKD. The score range is 1-4, where 1 means high level of stress associated with CKD and 4 means low level of stress associated with CKD.

    3. Level of energy/fatigue and emotional well-being as measured by the SF-36 mental health component [4 weeks]

      The SF-36 mental health component is a 9-item scale that measures energy/fatigue and emotional well-being in the past 4 weeks.Score range is 0-100, where 0 means poor emotional well-being and low energy and 100 means good emotional well-being and high energy.

    Other Outcome Measures

    1. Level of positive assessment of care as measured by the Patient Assessment of Care for Chronic Conditions (PACIC) scale [6 months]

      This is a 11-item scale evaluating patient assessment of the quality of care that patients received in the past 6 months. Score range is 1-5, where 1 means poor assessment of quality of care and 5 means good assessment of quality of care.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 18 years old or older

    • Have an estimated glomerular filtration rate (eGFR) of less than 60 ml/min/1.73 m2

    • Able to read and understand English without an interpreter

    • Diagnosed with chronic kidney disease on record

    Exclusion Criteria:
    • Patients with renal transplant or on dialysis

    • Patients who have documented or provider known cognitive impairment or vision impairment that will prohibit meaningful interaction with education activation worksheet

    • Patients who are not aware of their CKD diagnosis

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Canton Health Center Canton Michigan United States 48187
    2 Northville Health Center Northville Michigan United States 48168

    Sponsors and Collaborators

    • University of Michigan
    • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

    Investigators

    • Principal Investigator: Julie Wright-Nunes, MD, MPH, University of Michigan

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Julie Wright-Nunes, Associate Professor, University of Michigan
    ClinicalTrials.gov Identifier:
    NCT03084159
    Other Study ID Numbers:
    • HUM00118819
    • 4K23DK097183-04
    First Posted:
    Mar 20, 2017
    Last Update Posted:
    Sep 21, 2021
    Last Verified:
    Sep 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 21, 2021