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COordiNated CommuNication, Education, and Care Transitions After Acute Kidney Injury (CONNECT-AKI)

Recruiting

CONNECT-AKI: COordiNated CommuNication, Education, and Care Transitions After Acute Kidney Injury - A Pilot Randomized Controlled Trial

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Age 18 years or older
* Hospitalized with Stage 2 or Stage 3 acute kidney injury
* Kidney function has not returned to baseline at the time of hospital discharge
* Able to communicate in English
* Able to provide informed consent
* Willing and able to participate in study procedures independently or with assistance from a patient-designated care partner

Exclusion Criteria:

* Acute kidney injury requiring ongoing dialysis at the time of hospital discharge
* End-stage kidney disease
* Kidney transplant recipient
* Currently pregnant
* Documented cognitive impairment that precludes informed consent
* Receiving hospice or comfort-focused end-of-life care

About the study

The goal of this clinical trial is to learn whether different ways of providing information and follow-up support after acute kidney injury, also called AKI, can improve care transitions for adults being discharged from the hospital. AKI is a sudden decrease in kidney function that can occur during a hospital stay.

The main questions this study aims to answer are:

* Does an AKI discharge summary template improve communication about AKI after hospital discharge? * Does a chat-based educational messaging program improve patient understanding of AKI and support follow-up care after hospital discharge? * Researchers will compare usual care, an AKI discharge summary template, a chat-based educational messaging program, and the combination of the discharge summary template plus chat-based messaging.

Researchers will compare four groups:

* Usual care * An AKI discharge summary template * A chat-based educational messaging program * Both the AKI discharge summary template and the chat-based educational messaging program

Participants will complete questionnaires at the start of the study and about 4 weeks after hospital discharge. Participants will also receive a brief phone call about 3 months after discharge, and the research team will review their medical record for information about follow-up care, lab testing, emergency department visits, and hospital readmissions.

What is being tested

Sponsor: Northwell Health · Participants: 160 · Started: Jun 24, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07626268

Locations in the U.S.

New YorkLong Island Jewish Medical Center, Glen Oaks
North Shore University Hospital, Manhasset

Conditions

From ClinicalTrials.gov, data retrieved Nov 15, 2026. Each study sets its own eligibility; the study team decides who can join.