Chronic Kidney Disease Clinical Trial
Official title:
House Calls and Web-based Decision Support: Improving Access to Live Donor Kidney Transplantation
Verified date | July 2020 |
Source | Beth Israel Deaconess Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The main purpose of this research program is to reduce the burden of end-stage organ disease on individuals, families, healthcare systems, and society by increasing the availability of donor organs for transplantation. Consistent with this aim, the project further examines strategies to increase access to and reduce disparities - racial, economic, gender - in live donor kidney transplantation (LDKT). Specifically, we expand the research and intensity of an innovative House Calls intervention developed by the principal investigator by including other minorities and socioeconomically disadvantaged patients and by adding a novel Patient-Centered Decision Support component. The main study hypothesis is that participants receiving the novel intervention (House Calls + Patient-Centered Decision Support) will have a higher proportion of LDKT's by the 2-year study endpoint.
Status | Completed |
Enrollment | 109 |
Est. completion date | May 31, 2020 |
Est. primary completion date | May 31, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 21 Years and older |
Eligibility |
Inclusion Criteria: - non-White race/Hispanic ethnicity/low-income (250% below federal poverty guidelines) - CKD/ESRD - meets eligibility criteria for kidney transplant waiting list - 21 years old or older - self-reports being in LDKT Readiness Stage I, II, or III - Resides within 3 hours driving time from transplant center Exclusion Criteria: - Awaiting combined kidney-liver transplant - Awaiting simultaneous pancreas-kidney transplant - Know or suspected cognitive impairment - Prior participation in House Calls intervention study |
Country | Name | City | State |
---|---|---|---|
United States | Beth Israel Deaconess Medical Center | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Beth Israel Deaconess Medical Center | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Improvement in LDKT knowledge and LKDT readiness, reduced LDKT concerns and health care mistrust, greater amount of time spent discussing LDKT and higher quality interactions, and improvement in self-efficacy discussing LDKT. | 12 weeks | ||
Primary | The primary outcome for this study is the proportion of enrolled patients with live donor kidney transplants | 2 years | ||
Secondary | Higher proportion of enrolled patients with live donor inquires and evaluations; higher proportion of patients will be in LDKT Readiness stages 4/5 by the 12-week assessment. | 2 years |
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