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Controlling Hypertension Through Education and Coaching in Kidney Disease (CHECK-D)

Primary Purpose

Chronic Kidney Diseases, Chronic Disease, Chronic Kidney Disease, Stage 3 (Moderate)

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Control-EDI
Intervention-EDI and health coaching
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Kidney Diseases

Eligibility Criteria

21 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of CKD stage 3, 4, or 5 documented in medical record
  • Aware of CKD diagnosis
  • Has diagnosis of hypertension documented in medical record and most recent Blood Pressure (BP) within the last year meets criteria of uncontrolled hypertension (≥140 mmHg, and/or a diastolic blood pressure ≥90 mmHg noted in an ambulatory care setting within the past one year)
  • Estimated glomerular filtration rate (eGFR) of <60 within the last 18 months documented in the medical record

Exclusion Criteria:

  • Currently on dialysis permanently (i.e. are considered "end-stage renal disease" and receiving dialysis)
  • Previous kidney transplant
  • Pregnant (indicated by medical record or if patient self-identifies as pregnant)
  • Has cognitive, language, or vision impairment(s) that would prohibit participating in education, taking surveys, or participating in coaching activities
  • Has terminal illness

Sites / Locations

  • University of Michigan / Domino's FarmsRecruiting
  • University of Michigan / Briarwood Family MedicineRecruiting
  • University of Michigan / Brighton Health CenterRecruiting
  • University of Michigan / Canton Health CenterRecruiting
  • University of Michigan / Chelsea Health CenterRecruiting
  • University Health Center - GMAP/Gen MedRecruiting
  • University Health Center - Med PedsRecruiting
  • University of Michigan / Dexter Health CenterRecruiting
  • University of Michigan / Livonia Health CenterRecruiting
  • University of Michigan / Northville Health CenterRecruiting
  • University of Michigan / Ypsilanti Health CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control

Intervention

Arm Description

Eligible patients enrolled from the control group clinics will be given a Control-EDI which has information about kidney disease in general (not tailored to the patient) during their clinic visit.

Eligible patients enrolled from the intervention group clinics will be given an Intervention-EDI which has personalized information about kidney disease. There will be space on this for the provider to type in any goals or key points they want the patient to remember. Additionally, patients in this group will also receive health coaching.

Outcomes

Primary Outcome Measures

Change in Systolic Blood Pressure between baseline and 12 months
Changes in systolic blood pressure between baseline and 12 months will be compared between the intervention group and control group.

Secondary Outcome Measures

Change in Diastolic Blood Pressure between baseline and 12 months
Changes in diastolic blood pressure between baseline and 12 months will be compared between the intervention group and control group.
Slope of systolic BP between baseline and 12 months using all available BP values
BP will be collected at 4 time points - baseline, 1, 6, 12 months. This will be compared between the intervention group and control group.
Slope of diastolic BP between baseline and 12 months using all available BP values
BP will be collected at 4 time points - baseline, 1, 6, 12 months. This will be compared between the intervention group and control group.
CKD knowledge measured by the Kidney Knowledge Survey (KiKS)
This is a 28-item questionnaire measuring objective CKD disease knowledge and includes questions about goals, cardiovascular risk, and anti-hypertensive medications. Patients will answer the questions with a yes or no answer and their score will be based on how many responses were correct. This number will be converted to a percentage.
Medication Adherence Self-Efficacy Scale-Revised (MASES-R)
This is a 13-item measure with the answers on a Likert scale of 1 (not at all sure) to 4 (extremely sure). The higher the score the higher the self-efficacy, with a range from 13-52.
Morisky Medication Adherence Scale (MMAS - 8)
This scale is to quantify adherence to pharmacological treatments by 8 items. Levels of adherence are based on the following scores: <6 = low adherence; 6-<8 = medium adherence; 8 = high adherence.
Visit Time with provider
Length of time provider spends with the patient. This will be compared between the intervention group and control group.
Total time in clinic
Length of time between patient check-in and check-out. This will be compared between the intervention group and control group.
Patient Motivation by the Treatment Self-Regulation Questionnaire scale (TSRQ)
This contains a 17-item questionnaire in which the participants select scores from 1-7 or does not apply. A number of 1 = not at all and a score of 7 = considered very true, and zero = not applicable.
Satisfaction with CKD care based on Communication Assessment Tool (CAT)
This is a 15-item questionnaire that assesses the quality of physician to patient communication completed by the patients. There are 5 answers to choose from; poor, fair, good, very good, and excellent. The Score range is 1-5, where 1 means negative perception of communication and 5 means positive perception of communication.
Satisfaction with CKD care based on Consultation Care Measure (CCM)
This is a 21-item questionnaire that is completed by the patients, and select from the the 4 choices: very strongly agree, strongly agree, agree, and neutral/disagree. Each answer is worth one point on a Likert scale with a higher score meaning more satisfied.
Perceptions of health coaching for the intervention group
During health coach phone calls, participants will be asked 37 questions about their perceptions of the health coach program, including how much their participation in CHECK-D helped participants change various behaviors. Participant responses will be used to examine various measures of reliability and validity during the analyses of data acquired though this survey.
Medication adherence from the electronic medical record (EMR)
The EMR will be reviewed to evaluate the patients medication refills for adherence.
Self-efficacy for disease self-management based on The Perceived Kidney/Dialysis Self-Management Scale (PKDSMS)
This is an 8-item scale regarding self-efficacy where each statement is rated on the level of agreement from 1-5. 1 is disagree and 5 is agree.
Self-reported Blood Pressure-Related Behaviors Survey
This is a 5-item survey about knowledge and behaviors regarding sodium in the diet.
Provider Adoption based on EMR query and patient survey
Provider adoption will be measured by the percentage of enrolled patients whose providers used the EDI with them during their visit. Data will be collected by EMR query and a 1-item question in the patient survey.
Provider Fidelity measured by EMR query
Provider fidelity will be measured by the percentage of enrolled patients in the intervention clinics whose providers entered 1-2 patient specific goals in the EDI. This will be collected through EMR query.
Provider Perception of Usefulness by provider survey
Provider perception of usefulness will be measured by a survey of 2-3 questions about how useful they thought it was.
Change in serum creatinine
Change in Serum Creatinine between baseline and 12-months
Change in urine protein-creatinine ratio
Change in estimated glomerular filtration rate (eGFR)

Full Information

First Posted
August 24, 2019
Last Updated
May 8, 2023
Sponsor
University of Michigan
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
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1. Study Identification

Unique Protocol Identification Number
NCT04087798
Brief Title
Controlling Hypertension Through Education and Coaching in Kidney Disease
Acronym
CHECK-D
Official Title
Controlling Hypertension Through Education and Coaching in Kidney Disease
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 4, 2020 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic kidney disease (CKD) is a serious and growing public health problem. The purpose of this study is to find out if an educational worksheet, called the Encounter Decision Intervention (EDI), combined with health coaching helps CKD patients improve their blood pressure and other health outcomes. The research team hypothesizes that the intervention group will have greater improvement in CKD outcomes than the control group.
Detailed Description
Patients that meet eligibility criteria and are seen in a clinic assigned to the control group will be given a Control-Encounter Decision Intervention (Control-EDI) about kidney disease in general (not tailored to the patient) by their primary care provider. Eligible patients that agree to participate and give consent will complete enrollment, 1, 6, and 12 month follow-up visits. Eligible patients that are seen in a clinic assigned to the intervention group will be given a personalized Intervention-EDI by their primary care provider. Following this, eligible patients that agree to participate and give consent will complete the enrollment visit, and have a baseline call with a health coach. In addition to the 1, 6, 12 month follow-up visits these patients will also have approximately 4-6 phone calls with the health coach between the baseline visit and 11 months after enrollment. In both groups the study team will be collecting medical information and assessments regarding their health; blood sample and urine samples at baseline and 12 months; approximately 4-6 phone calls; as well as surveys at various time points. In order to reduce in-person human subject activity due to the Coronavirus disease 2019 (COVID-19) pandemic, participants in both groups receive an at home blood pressure monitor so that systolic- & diastolic-BP data can be collected at all 4 time points (baseline, 1, 6, 12 months).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Diseases, Chronic Disease, Chronic Kidney Disease, Stage 3 (Moderate), Chronic Kidney Disease, Stage 4 (Severe), Chronic Kidney Disease Stage 5

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Cluster Randomized Design
Masking
None (Open Label)
Allocation
Randomized
Enrollment
350 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Active Comparator
Arm Description
Eligible patients enrolled from the control group clinics will be given a Control-EDI which has information about kidney disease in general (not tailored to the patient) during their clinic visit.
Arm Title
Intervention
Arm Type
Experimental
Arm Description
Eligible patients enrolled from the intervention group clinics will be given an Intervention-EDI which has personalized information about kidney disease. There will be space on this for the provider to type in any goals or key points they want the patient to remember. Additionally, patients in this group will also receive health coaching.
Intervention Type
Behavioral
Intervention Name(s)
Control-EDI
Other Intervention Name(s)
Control-Encounter Decision Intervention
Intervention Description
Patients in the control group will receive Control-EDI from their primary care provider during clinic visit. Subsequent patient CKD education and follow-up will be provider dependent. Patients will be called and reminded of their study visits at 1, 6, 12 months to complete study measures, BP checks, and give urine and blood samples (baseline and 12-month visit only).
Intervention Type
Behavioral
Intervention Name(s)
Intervention-EDI and health coaching
Other Intervention Name(s)
Intervention-Encounter Decision Intervention
Intervention Description
Patients in the intervention group will receive a personalized Intervention-EDI from their primary care provider during visit, which will include their most recent BP, their urine protein level and most recent eGFR. There is also a space for their provider to type in a sentence about specific goals for the patient. Health coaches will conduct a baseline call and 4-6 coaching calls, based on patient's needs, over an 11-month period. There are 4 topic areas related to blood pressure and CKD that will be the focus of the calls. Coaches will also have pre-determined and vetted educational resources to provide patients if needed. Additionally, patients will be called and reminded of their study visits at 1, 6, 12 months to complete study measures, BP checks, and give urine and blood samples (baseline and 12-month visit only).
Primary Outcome Measure Information:
Title
Change in Systolic Blood Pressure between baseline and 12 months
Description
Changes in systolic blood pressure between baseline and 12 months will be compared between the intervention group and control group.
Time Frame
Baseline, 12 months
Secondary Outcome Measure Information:
Title
Change in Diastolic Blood Pressure between baseline and 12 months
Description
Changes in diastolic blood pressure between baseline and 12 months will be compared between the intervention group and control group.
Time Frame
Baseline, 12 months
Title
Slope of systolic BP between baseline and 12 months using all available BP values
Description
BP will be collected at 4 time points - baseline, 1, 6, 12 months. This will be compared between the intervention group and control group.
Time Frame
Baseline up to 12 months
Title
Slope of diastolic BP between baseline and 12 months using all available BP values
Description
BP will be collected at 4 time points - baseline, 1, 6, 12 months. This will be compared between the intervention group and control group.
Time Frame
Baseline up to 12 months
Title
CKD knowledge measured by the Kidney Knowledge Survey (KiKS)
Description
This is a 28-item questionnaire measuring objective CKD disease knowledge and includes questions about goals, cardiovascular risk, and anti-hypertensive medications. Patients will answer the questions with a yes or no answer and their score will be based on how many responses were correct. This number will be converted to a percentage.
Time Frame
Baseline up to 12 months
Title
Medication Adherence Self-Efficacy Scale-Revised (MASES-R)
Description
This is a 13-item measure with the answers on a Likert scale of 1 (not at all sure) to 4 (extremely sure). The higher the score the higher the self-efficacy, with a range from 13-52.
Time Frame
Baseline up to 12 months
Title
Morisky Medication Adherence Scale (MMAS - 8)
Description
This scale is to quantify adherence to pharmacological treatments by 8 items. Levels of adherence are based on the following scores: <6 = low adherence; 6-<8 = medium adherence; 8 = high adherence.
Time Frame
Baseline up to 12 months
Title
Visit Time with provider
Description
Length of time provider spends with the patient. This will be compared between the intervention group and control group.
Time Frame
Enrollment visit (baseline)
Title
Total time in clinic
Description
Length of time between patient check-in and check-out. This will be compared between the intervention group and control group.
Time Frame
Enrollment visit (baseline)
Title
Patient Motivation by the Treatment Self-Regulation Questionnaire scale (TSRQ)
Description
This contains a 17-item questionnaire in which the participants select scores from 1-7 or does not apply. A number of 1 = not at all and a score of 7 = considered very true, and zero = not applicable.
Time Frame
Baseline up to 12 months
Title
Satisfaction with CKD care based on Communication Assessment Tool (CAT)
Description
This is a 15-item questionnaire that assesses the quality of physician to patient communication completed by the patients. There are 5 answers to choose from; poor, fair, good, very good, and excellent. The Score range is 1-5, where 1 means negative perception of communication and 5 means positive perception of communication.
Time Frame
Baseline up to 12 months
Title
Satisfaction with CKD care based on Consultation Care Measure (CCM)
Description
This is a 21-item questionnaire that is completed by the patients, and select from the the 4 choices: very strongly agree, strongly agree, agree, and neutral/disagree. Each answer is worth one point on a Likert scale with a higher score meaning more satisfied.
Time Frame
Baseline up to 12 months
Title
Perceptions of health coaching for the intervention group
Description
During health coach phone calls, participants will be asked 37 questions about their perceptions of the health coach program, including how much their participation in CHECK-D helped participants change various behaviors. Participant responses will be used to examine various measures of reliability and validity during the analyses of data acquired though this survey.
Time Frame
Baseline up to 12 months
Title
Medication adherence from the electronic medical record (EMR)
Description
The EMR will be reviewed to evaluate the patients medication refills for adherence.
Time Frame
Baseline up to 12 months
Title
Self-efficacy for disease self-management based on The Perceived Kidney/Dialysis Self-Management Scale (PKDSMS)
Description
This is an 8-item scale regarding self-efficacy where each statement is rated on the level of agreement from 1-5. 1 is disagree and 5 is agree.
Time Frame
Baseline up to 12 months
Title
Self-reported Blood Pressure-Related Behaviors Survey
Description
This is a 5-item survey about knowledge and behaviors regarding sodium in the diet.
Time Frame
Baseline up to 12 months
Title
Provider Adoption based on EMR query and patient survey
Description
Provider adoption will be measured by the percentage of enrolled patients whose providers used the EDI with them during their visit. Data will be collected by EMR query and a 1-item question in the patient survey.
Time Frame
Baseline
Title
Provider Fidelity measured by EMR query
Description
Provider fidelity will be measured by the percentage of enrolled patients in the intervention clinics whose providers entered 1-2 patient specific goals in the EDI. This will be collected through EMR query.
Time Frame
Baseline
Title
Provider Perception of Usefulness by provider survey
Description
Provider perception of usefulness will be measured by a survey of 2-3 questions about how useful they thought it was.
Time Frame
Baseline up to 12 months
Title
Change in serum creatinine
Description
Change in Serum Creatinine between baseline and 12-months
Time Frame
Baseline, 12 months
Title
Change in urine protein-creatinine ratio
Time Frame
Baseline, 12 months
Title
Change in estimated glomerular filtration rate (eGFR)
Time Frame
Baseline, 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of CKD stage 3, 4, or 5 documented in medical record Aware of CKD diagnosis Has diagnosis of hypertension documented in medical record and most recent Blood Pressure (BP) within the last year meets criteria of uncontrolled hypertension (≥140 mmHg, and/or a diastolic blood pressure ≥90 mmHg noted in an ambulatory care setting within the past one year) Estimated glomerular filtration rate (eGFR) of <60 within the last 18 months documented in the medical record Exclusion Criteria: Currently on dialysis permanently (i.e. are considered "end-stage renal disease" and receiving dialysis) Previous kidney transplant Pregnant (indicated by medical record or if patient self-identifies as pregnant) Has cognitive, language, or vision impairment(s) that would prohibit participating in education, taking surveys, or participating in coaching activities Has terminal illness
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Julie Wright
Phone
734-764-5178
Email
juwright@med.umich.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Ying-Jen Lin
Email
yingjen@umich.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julie Wright, MD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan / Domino's Farms
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48105
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pamela Rockwell, DO
Facility Name
University of Michigan / Briarwood Family Medicine
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48108
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Keri Denay, MD
Facility Name
University of Michigan / Brighton Health Center
City
Brighton
State/Province
Michigan
ZIP/Postal Code
48116
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mark Ealovega, MD
Facility Name
University of Michigan / Canton Health Center
City
Canton
State/Province
Michigan
ZIP/Postal Code
48187
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Floyd Brinley, MD
Facility Name
University of Michigan / Chelsea Health Center
City
Chelsea
State/Province
Michigan
ZIP/Postal Code
48118
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jill Fenske, MD
Facility Name
University Health Center - GMAP/Gen Med
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kellie Lazarek
Phone
313-745-0160
Facility Name
University Health Center - Med Peds
City
Detroit
State/Province
Michigan
ZIP/Postal Code
48201
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kellie Lazarek, MHA
Phone
313-745-0160
Facility Name
University of Michigan / Dexter Health Center
City
Dexter
State/Province
Michigan
ZIP/Postal Code
48130
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Manasi Ramakrishnan, MD
Facility Name
University of Michigan / Livonia Health Center
City
Livonia
State/Province
Michigan
ZIP/Postal Code
48152
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christine Medaugh, MD
Facility Name
University of Michigan / Northville Health Center
City
Northville
State/Province
Michigan
ZIP/Postal Code
48168
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Audrey Fan, MD
Facility Name
University of Michigan / Ypsilanti Health Center
City
Ypsilanti
State/Province
Michigan
ZIP/Postal Code
48198
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ebony Parker-Featherstone, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Controlling Hypertension Through Education and Coaching in Kidney Disease

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