- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04806126
Evaluation of a Virtual Home Dialysis Mentoring Program (Home) (HOME)
The Investigator plans to establish a virtual platform for home dialysis physician mentoring with the intent to:
- Formulate a practical, interactive, virtual curriculum in home dialysis
- Provide dedicated video conferences in home dialysis mentorship
- Measure knowledge awareness and attitudes towards home dialysis
Study Overview
Status
Conditions
Detailed Description
Home-based kidney replacement therapy offers enhanced quality of life and clinical advantages compared to conventional in-center hemodialysis. Globally, there is an increased awareness of home dialysis. However, there is a lack of mentoring centers to support new programs and/or nephrologists to initiate and grow home dialysis.1, 2 Critical prerequisites for a successful mentoring relationship include:
- Established excellence in home dialysis in the mentor center
- Willingness from both mentors and mentees to participate in the program
- Engaging, high quality clinical content, including sharing of best practices
- Lack of system barriers to establish home dialysis
- Dedicated metrics to measure success of the program
The Investigator plans to establish a virtual platform with the intent to:
- Formulate a practical, interactive, virtual curriculum in home dialysis
- Provide dedicated video conferences in home dialysis mentorship
- Measure knowledge awareness and attitudes towards home dialysis
The Investigator hypothesizes that an effective, sustained mentorship program will increase knowledge and awareness of home dialysis and will ultimately enhance overall home dialysis adoption.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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California
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San Jose, California, United States, 95128
- Satellite Healthcare, Inc.
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Credentialed physicians at Satellite Healthcare
- Nephrology fellows at nephrology training program affiliated with Satellite Healthcare credentialed physician
Exclusion Criteria:
- Any person who does not meet the inclusion criteria
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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Virtual Mentoring Program Participants
Physicians credentialed at Satellite Healthcare will be eligible to participate along with nephrology fellows from training programs affiliated with credentialed physicians.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The change in participants' self-reported knowledge awareness.
Time Frame: through study completion, an average of 1 year
|
The change in participants' self-reported knowledge awareness (as assessed by self- reported expertise rating).
|
through study completion, an average of 1 year
|
The change in participants' perception of home dialysis adoption
Time Frame: through study completion, an average of 1 year
|
The change in participants' perception of home dialysis adoption as assessed by the percentage of home dialysis patients relative to conventional in-center hemodialysis at baseline versus the end of the study.
|
through study completion, an average of 1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of registered participants
Time Frame: through study completion, an average of 1 year
|
Number of physicians who register for the program
|
through study completion, an average of 1 year
|
Number of participants attending each session
Time Frame: through study completion, an average of 1 year
|
Number of physicians who participate in each mentoring Session
|
through study completion, an average of 1 year
|
Change in the percentage of patients using home dialysis
Time Frame: through study completion, an average of 1 year
|
Change between baseline and end of study in the number of home dialysis patients
|
through study completion, an average of 1 year
|
Collaborators and Investigators
Sponsor
Publications and helpful links
General Publications
- Mehrotra R, Blake P, Berman N, Nolph KD. An analysis of dialysis training in the United States and Canada. Am J Kidney Dis. 2002 Jul;40(1):152-60. doi: 10.1053/ajkd.2002.33924.
- Liebman SE, Moore CA, Monk RD, Rizvi MS. What Are We Doing? A Survey of United States Nephrology Fellowship Program Directors. Clin J Am Soc Nephrol. 2017 Mar 7;12(3):518-523. doi: 10.2215/CJN.06530616. Epub 2016 Dec 5.
- Becevic M, Mutrux R, Edison K. Show-Me ECHO: Complex Disease Care Capacity-Building Telehealth Program. Stud Health Technol Inform. 2016;226:233-6.
- Lewiecki EM, Rochelle R, Bouchonville MF 2nd, Chafey DH, Olenginski TP, Arora S. Leveraging Scarce Resources With Bone Health TeleECHO to Improve the Care of Osteoporosis. J Endocr Soc. 2017 Nov 6;1(12):1428-1434. doi: 10.1210/js.2017-00361. eCollection 2017 Dec 1.
- King AM, Gottlieb M, Mitzman J, Dulani T, Schulte SJ, Way DP. Flipping the Classroom in Graduate Medical Education: A Systematic Review. J Grad Med Educ. 2019 Feb;11(1):18-29. doi: 10.4300/JGME-D-18-00350.2.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- SP132_Home
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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