Acute Kidney Injury In Care Transitions (ACT): Pragmatic Clinical Trial
Part of paid clinical trials in Mankato, Minnesota.
- Sponsor
- Mayo Clinic
- Study ID
- NCT07670520
- Status
- Recruiting
Conditions
- Acute Kidney Injury
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Acute Kidney Injury in Care Transitions (ACT) — BEHAVIORALClinicians will assign risk-individualized kidney health care prior to hospital discharge for acute kidney injury survivors. Low risk acute kidney injury survivors will receive education prior to hospital discharge, moderate risk acute kidney injury survivors will receive a referral to primary care for laboratory and clinical follow-up within approximately 14-days including a medication review by a pharmacist, and high risk acute kidney injury survivors will be referred to nephrologist-directed care including remote monitoring program (RPM) where available and aligned with the patients goals/values/preferences for up to 90 days after discharge for the highest risk patients.
- Usual Care — BEHAVIORALPhysicians and nurse practitioners will provide standard of care education, labs, and clinical follow-up after discharge.
Study Details
The purpose of this study is to determine the effect of a multidisciplinary intervention at care transitions for acute kidney injury survivors on patient-centered outcomes.
Key Dates
- Start date
- Apr 16, 2026
- Status verified
- Jun 2026
- Primary completion
- Mar 31, 2030
- Completion
- Dec 31, 2030
Study Design
- Enrollment
- 2,260 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- PREVENTION
Arms
- Experimental: Acute Kidney Injury in Care Transitions (ACT) InterventionPhysicians and nurse practitioners randomized to the ACT intervention group will be provided access to augmented kidney care support for acute kidney injury patients prior to hospital discharge, individualized according to post-discharge risk.
- Active Comparator: Usual CarePhysicians and nurse practitioners randomized to the usual care group will provide standard of care education, labs, and clinical follow-up after discharge.
Primary Outcome Measure
Hospital-Free Days [ Time Frame: 90 days, 180 days, 1 year ]
Central Contacts
- Mitchell C. Strand507-293-0952
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Mayo Clinic Health System-Mankato | Mankato | Minnesota | 56001 | Mitchell C. Strand 507-293-0952 Jing Miao, M.D., Ph.D. (PRINCIPAL_INVESTIGATOR) |
| Mayo Clinic in Rochester | Rochester | Minnesota | 55905 | Mitchell C. Strand 507-293-0952 Erin F. Barreto, Pharm.D., Ph.D. (PRINCIPAL_INVESTIGATOR) |
| Mayo Clinic Health System-Eau Claire Clinic | Eau Claire | Wisconsin | 54703 | Mitchell C. Strand 507-293-0952 Suhail B Shuja, M.D. (PRINCIPAL_INVESTIGATOR) |
Find similar trials in Mankato, MN
Related Studies
- Improving Continuous Renal Replacement Therapy Outcomes in Neonates and Infants Through Interdisciplinary CollaborationEnrolling By Invitation · Children's Hospital Medical Center, Cincinnati · Palo Alto, California
- SAfety of Regional Citrate Anticoagulation (SARCA Study)PHASE3 · Recruiting · Fresenius Medical Care North America · Little Rock, Arkansas
- Neutrophil and Monocyte Deactivation Via the SeLective CytopheretIc Device - A Randomized Clinical Trial in Acute Kidney InjuryRecruiting · SeaStar Medical · Birmingham, Alabama
- Combining Biomarkers and Electronic Risk Scores to Predict AKI in Hospitalized PatientsRecruiting · University of Chicago · Chicago, Illinois