Chronic Kidney Disease Clinical Trial
— ExPANDOfficial title:
Improving Shared Decision-Making and Access to Non-Dialytic Treatment for People With Kidney Disease (The ExPAND Trial)
The goal of this clinical trial is to compare two health system-based approaches for offering kidney failure treatment options to older patients with kidney failure, specifically, to ensure patients are actively involved in a shared decision making (SDM) process covering a full range of treatment choices and have meaningful access to that full range of choices. These include standard in-center or home dialysis as well as alternative treatment plans (ATPs): active medical care without dialysis, time-limited trial of dialysis, palliative dialysis, and deciding not to decide. Approach 1 - Educate and Engage: Nephrology practices encourage their patients to a) participate in a kidney disease education program providing a balanced presentation of all options including ATPs, b) use evidence-based patient decision aids that include ATPs, and c) engage in SDM with staff trained in communication skills and best practices. Approach 2 - Educate and Engage Plus Kidney Supportive Care Program: Nephrology practices add a primary palliative care program to support patients who choose ATPs and their families. The program provides care coordination, symptom management, advance care planning, and psychosocial support to supplement usual care from their nephrologist. To compare the two approaches, the investigators will conduct a repeated, cross-sectional stepped wedge cluster randomized trial involving 28 chronic kidney disease clinics at 10 practice organizations around the United States. Aim 1: Compare the effectiveness of Approaches 1 and 2 in a) increasing proportion of patients choosing ATP and b) reducing patient-reported decisional conflict about treatment. Aim 2: Compare the patient and family experience of ATP care between Approaches 1 and 2 in terms of quality of life, services used, and end of life (EOL) experience. Aim 2a will focus on experience while patients are receiving an ATP. Aim 2b will describe the EOL experience. Aim 3: Evaluate implementation of each approach through a mixed-methods design based on the expanded RE-AIM framework. For Aims 1 and 2, researchers will collect information by chart review and surveys with patients and caregivers. For Aim 3, information will be reported by site managers as part of monthly progress reports. Clinic administrators, clinical providers, and staff will complete surveys before and after implementation of each approach.
Status | Not yet recruiting |
Enrollment | 3000 |
Est. completion date | June 1, 2028 |
Est. primary completion date | December 31, 2027 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 65 Years and older |
Eligibility | Study Population 1: Person with CKD, cared for at participating clinic Inclusion Criteria: - Age 65 years or older - eGFR dropped below 20 at least once during past 12 months. (The patient is still eligible if there are some results just above this range, e.g., 20-25, at screening or during follow up.) Exclusion Criteria: - The eGFR measurement(s) below 20 are considered to be due to acute kidney injury by the clinical team. - The patient is a candidate for kidney transplant - KDE was initiated before screening. (The patient is still eligible if 1) KDE was initiated within the month before screening or 2) KDE occurred when eGFR >= 20.) Exclusion Criteria for surveys and interviews: - Insufficient decision making capacity - Non-English and non-Spanish speaking - Treating nephrologist/APP opts patient out (for example, if contraindicated for patient's health) - After eGFR < 20, KDE already attended (first survey only) Study Population 2: Family member or caregiver of patient in Study Population 1 Inclusion Criteria: - Family member or caregiver of Population 1 patient who has chosen alternative treatment plan - 18+ years old - English or Spanish speaking - Cognitively able to participate in surveys/interviews Study Population 3: Administrator, clinical provider, or staff at participating chronic kidney disease clinic Inclusion Criteria: - Currently practicing or employed at participating clinic |
Country | Name | City | State |
---|---|---|---|
United States | Dallas Nephrology Associates | Dallas | Texas |
United States | Ochsner Health | Jefferson | Louisiana |
United States | West Virginia University Medicine | Morgantown | West Virginia |
United States | The Rogosin Institute | New York | New York |
United States | Renalcare Associate | Peoria | Illinois |
United States | Medstar Washington Hospital Center | Washington | District of Columbia |
Lead Sponsor | Collaborator |
---|---|
George Washington University | Patient-Centered Outcomes Research Institute, University of Bristol, West Virginia University Research Corporation |
United States,
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* Note: There are 33 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | McGill Quality of Life score | McGill Quality of Life score (Cohen et al., 1997). Based on responses to 16 items, scores range from 0 (worst quality of life) to 160 (best quality of life). Repeated measure, reported by a convenience sample of patients who choose an ATP and participate in a longitudinal series of interviews. | Starts after consent to participate in longitudinal interviews. Repeats every 4 months until first of project completion or patient death, assessed up to 40 months. | |
Other | Quality of Communication Questionnaire: general communication skills scale score | Engelberg Quality of Communication Questionnaire (Engelberg et al., 2006) 6-item general communications skills scale measures quality of doctor-patient communication. Scored as 0 (very worst possible) to 10 (very best possible). Repeated measure, reported by a convenience sample of patients who choose an ATP and participate in a longitudinal series of interviews. | Starts after consent to participate in longitudinal interviews. Repeats every 4 months until first of project completion or patient death, assessed up to 40 months. | |
Other | Quality of Communication Questionnaire: communication about end-of-life care scale score | Engelberg Quality of Communication Questionnaire (Engelberg et al., 2006) 7-item communication about end-of-life care scale measures quality of doctor-patient communication about end-of-life care. Scored as 0 (very worst possible) to 10 (very best possible). Repeated measure, reported by a convenience sample of patients who choose an ATP and participate in a longitudinal series of interviews. | Starts after consent to participate in longitudinal interviews. Repeats every 4 months until first of project completion or patient death, assessed up to 40 months. | |
Other | ATP patient reports of experience of ATP care (qualitative) | Responses to open-ended questions about the experience of receiving care under an alternative treatment plan. Reported by a convenience sample of patients who choose an ATP and participate in a longitudinal series of interviews. | Starts after consent to participate in longitudinal interviews. Repeats every 4 months until first of project completion or patient death, assessed up to 40 months.] | |
Other | Caregiver reports of caregiving experience (qualitative) | Responses to open-ended questions of experience caring for patients who have selected ATP. Reported by a convenience sample of caregivers who have consented to participate in a longitudinal series of interviews. | Starts after consent to participate in longitudinal interviews. Repeats every 4 months until first of project completion or patient death, assessed up to 40 months. | |
Other | Hospice use by ATP patients | Among ATP patients, proportion of deaths with hospice care, length of use of hospice. | End of life. Collected by chart review 3 months after death. | |
Other | Family rating of quality of care at end of life (EOL) and themes about it | Selected questions from Bereaved Family Survey (US Department of Veterans Affairs). Qualitative themes from interview. | End of life. Family members will be approached 4 months after death. | |
Other | Reach: Proportion of eligible patients who enroll in and complete KDE | Proportion of eligible patients who enroll in and complete KDE. Demographic representativeness will be also be described. | Reported monthly by site manager in monthly progress reports, assessed from start to end of study, up to 40 months | |
Other | Proportion of eligible patients who enroll in the Kidney Supportive Care Program | Proportion of eligible patients (patients who choose an ATP under Approach 2) who enroll in the Kidney Supportive Care Program. Demographic representativeness will be also be described. | Reported monthly by site manager in monthly progress reports, assessed from start to end of study, up to 40 months | |
Other | Implementation (fidelity) | Fidelity checklists | Assessed 3 times at each clinical site through study completion, once after initial training for approach 1, once during the month prior to starting approach 2, and once during the last month of the study | |
Other | Maintenance (Organizational) | Program sustainability assessment tool | Assessed 3 times at each clinical site through study completion, once after initial training for approach 1, once during the month prior to starting approach 2, and once during the last month of the study | |
Other | Acceptability (Organizational) | Acceptability of Intervention Measure and Semi-structured interviews | Assessed 3 times at each clinical site through study completion, once after initial training for approach 1, once during the month prior to starting approach 2, and once during the last month of the study | |
Other | Appropriateness (Organizational) | Intervention Appropriateness Measure and Semi-structured interviews | Assessed 3 times at each clinical site through study completion, once after initial training for approach 1, once during the month prior to starting approach 2, and once during the last month of the study | |
Other | Feasibility (Organizational) | Feasibility of Intervention Measure and Semi-structured interviews | Assessed 3 times at each clinical site through study completion, once after initial training for approach 1, once during the month prior to starting approach 2, and once during the last month of the study | |
Other | Inner Setting, Implementation Process, Individuals (Organizational) | Staff will be surveyed with questions like E.g., What types of additional support do you feel you most need to continue using shared decision- making? E.g., Are there people in your practice who are likely to champion the Kidney Supportive Care Program? E.g., How do you feel about the Kidney Disease Education being used in your clinic? | Assessed 2 times at each clinical site through study completion, once during the month prior to starting approach 2, and once during the last month of the study | |
Primary | Proportion of patients choosing Alternative Treatment Plans (ATP) | Numerator: number of patients choosing an alternative treatment plan. Denominator: enrolled patients with decision-making capacity. | From initiation of treatment decision-making process to four months later. | |
Primary | Decisional Conflict Scale score | Decisional Conflict Scale (O'Connor, 1995) score at month 3 survey, adjusted for baseline score. Score ranges from 0 (no decisional conflict) to 100 (extremely high decisional conflict). | Month 3 after treatment decision-making process initiated. | |
Secondary | Rating of CKD Knowledge Among Older Adults (Know-CKD) score | Rating of CKD Knowledge Among Older Adults (Know-CKD) 3 months after initiation of treatment decision-making processDecision-Aid for Renal Therapy (DART) Knowledge Assessment (Ladin et al., 2023). The DART survey contains 10 items scored on a 3 point scale, with 0 points given for an answer of yes, 2 for an answer of unsure, and 4 for an answer of no. The total score is the sum of the 10 items, multiplied by 2.5. The minimum score possible is 0 (no decisional conflict) and the maximum score possible is 100 (extremely high decisional conflict) (Month three score, adjusted for baseline score) | Three months after initiation of treatment decision-making process. | |
Secondary | Shared Decision Making Questionnaire (SDM-Q-9) score | 9-Item Shared Decision Making Questionnaire (SDM-Q-9) score (Scholl, 2010) from telephone survey. Score ranges from 0 (least SDM) to 45 (most SDM). | Month 4 after treatment decision-making process initiated. | |
Secondary | CollaboRATE score | CollaboRATE score (Elwyn et al., 2013) from telephone survey. Scores range from 0 (least SDM) to 9 (most SDM). | Month 4 after treatment decision-making process initiated. | |
Secondary | Patient reported decision regret | Modification of dialysis decision regret (Saeed et al., 2020) : Do you regret your decision to start (treatment selected) elicited during telephone survey. | Month 4 after treatment decision-making process initiated. | |
Secondary | Advance care planning (ACP) documentation | Complete ACP measure (Three elements present in chart: a surrogate, a goals of care discussion, and either an accessible advance directive or medical order such as POLST or DNR.) | Month 4 after treatment decision-making process initiated. | |
Secondary | Proportion of Active Medical Care Without Dialysis (AMCWD) patients who change to dialysis at any time | Proportion of patients who initially choose AMCWD who subsequently switch to dialysis (standard in-center hemodialysis, home dialysis, time-limited trial, or palliative). | From date of initial treatment decision to date of changed treatment decision, start of dialysis, patient death or end of study, whichever came first, assessed up to 40 months. | |
Secondary | Proportion of ATP patients who have an unplanned transition into dialysis | Proportion of patients who initially choose an ATP who subsequently have an unplanned dialysis start: defined as starting dialysis urgently in the hospital during an unscheduled admission. | From date of initial treatment decision to date of changed treatment decision, start of dialysis, patient death or end of study, whichever came first, assessed up to 40 months. | |
Secondary | End of Life intensity scale | Modified scale adapted from Wong et al, 2012, based on health services received during the last month of life (dialysis, emergency department, hospital, ICU), and death in hospital. Scores range from 0-6 with a higher score indicating more intensive end-of-life care. | Final 30 days of life, (60 days and 90 days for sensitivity analysis). Assessed 3 months after patient death. | |
Secondary | AMCWD & DND patients who initiate dialysis in the last month of life | Of AMCWD & DND patients die during the study, proportion who used dialysis in last 30 days of life. | Final 30 days of life, (60 days and 90 days for sensitivity analysis). Assessed 3 months after patient death. | |
Secondary | For ATP patients, advance care planning (ACP) documentation at time of death. | Complete ACP measure (Three elements present in chart: a surrogate, a goals of care discussion, and either an accessible advance directive or medical order such as POLST or DNR.) | Time of death. Collected 3 months after patient death. | |
Secondary | Proportion of eligible clinicians who engage patients in Shared Decision Making (SDM) | Proportion of eligible clinicians who engage patients in SDM. Demographic representativeness will be also be described. | Reported monthly by site manager in monthly progress reports, assessed from start to end of study, up to 40 months | |
Secondary | Proportion of eligible clinicians who increase the proportion of patients choosing ATP | Proportion of eligible clinicians who increase the proportion of patients choosing ATP. Demographic representativeness will be also be described. | Reported monthly by site manager in monthly progress reports, assessed from start to end of study, up to 40 months | |
Secondary | Proportion of eligible practice sites that offer Kidney Disease Education (KDE) | Proportion of eligible practice sites that offer KDE. Demographic representativeness will be also be described. | Reported monthly by site manager in monthly progress reports, assessed from start to end of study, up to 40 months | |
Secondary | Proportion of eligible practice sites that offer Kidney Supportive Care (KSC) program | Proportion of eligible practice sites that offer KSC. Demographic representativeness will be also be described. | Reported monthly by site manager in monthly progress reports, assessed from start to end of study, up to 40 months |
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