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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05184894
Other study ID # 21-011055
Secondary ID R03HS028060-01
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date January 17, 2022
Est. completion date November 2024

Study information

Verified date March 2024
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This research is being done to develop materials and processes that will help facilitate education and kidney care coordination for AKI survivors.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 50
Est. completion date November 2024
Est. primary completion date October 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Participants will be recruited from those identified by a developed electronic health record list of patients with stage III AKI (severe) during a hospitalization based on serum creatinine rise or urine output decline from Olmsted County. Exclusion Criteria: - Dementia. - Non-English speaking. - Expected to be dismissed to a skilled nursing facility or hospice at discharge. - Expected to need dialysis at discharge. - Primary Care Transitions Program enrollment. - Transplant recipients within 100 days of transplant. - Can only have one time enrollment.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
AKI in Care Transitions (ACT) program
Multicomponent transitional support bundle that includes consultation from nurse educators before discharge to deliver kidney health education and coordination of appointments post-discharge.

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (2)

Lead Sponsor Collaborator
Mayo Clinic Agency for Healthcare Research and Quality (AHRQ)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of subjects to complete the ACT program Total number of subjects to complete the full ACT program intervention 30 days after hospitalization
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