Understanding the Role of Patient Behavior Change in Improving AKI Outcomes

Not Applicable

Completed

• Conditions: Acute Kidney Injury
• Interventions: Other: mHealth tool

• Registration Number: NCT03114592
• Lead Sponsor: Duke University

Brief Summary

This study is looking to improve the safety of patients with acute kidney injury via education provided on a mobile tablet. This study will additionally examine if electronic tools, such as mobile tablets, can help.

Detailed Description

Acute kidney injury (AKI) is an increasingly common complication of acute hospitalizations. Hospital-related AKI, commonly caused by hemodynamic changes or contrast exposure, carries a threat of adverse outcomes that persists following hospital discharge, with an independent and graded association with long-term mortality. It is estimated that, approximately 13% of individuals with acute coronary syndrome (ACS) will develop some degree of AKI during their hospitalization. Survivors of AKI consume significantly greater health resources than the general population, and suffer exceedingly poor renal outcomes, including persistent loss of kidney function, progression to end stage renal disease (ESRD), and increased risk of recurrent AKI. It is estimated that 25% of individuals with an AKI-related hospitalization will be readmitted with recurrent AKI within 12 months of discharge, highlighting a critical need to address ongoing AKI risk once the acute hospitalization is complete. Patient-centered educational interventions that intensify awareness of potentially hazardous situations may reduce AKI recurrence. For example, commonly prescribed therapies such as diuretics or ACE inhibitors may threaten the renal safety of individuals at high risk of recurrent AKI if taken when significantly volume deplete, such as during an acute gastroenteritis, and in most cases should be held until one can eat and drink normally; Nonsteroidal Anti-inflammatory Drugs (NSAIDs) may exacerbate AKI risk if taken in combination with diuretics or ACE inhibitors even when volume replete and should be completely avoided. Tailored educational curricula surrounding these and other topics pertinent to AKI survivors may reduce recurrent hospitalizations and lower healthcare costs. In the absence of a patient centered outpatient approach to AKI education, the development of effective and sustainable AKI prevention strategies remains unlikely.

Our long-term goal is to develop patient-centered educational materials to reduce AKI recurrence. We hypothesize that a tailored educational curriculum will improve patient awareness of potential hazards and reduce AKI recurrence among hospital-based AKI survivors. Therefore, our overall objective for this proposal is to pilot test and evaluate the feasibility of a patient-centered mobile health (mHealth) educational curriculum for hospitalized AKI survivors at Duke Medical Center.

Aim 1: To test the feasibility and acceptance of a mHealth patient safety curriculum in hospitalized AKI survivors.

Hypothesis 1: Patient safety risk awareness at 1 month will be higher in the educational intervention arm than the usual care arm.

Aim 2: To determine if a mHealth educational curriculum improves patient safety behaviors in AKI survivors.

Hypothesis 2: High-risk safety behaviors will be reduced at 1 month in AKI survivors receiving the educational intervention, but not in the usual care arm.

Study Timeline

• Study First Submitted: 2017-04-11
• Study First Submitted QC: 2017-04-13
• Study First Posted: 2017-04-14
• Study Start: 2017-06-16
• Status Verified: 2018-07
• Primary Completion: 2018-08-27
• Study Completion: 2018-08-27
• Last Update Submitted: 2018-12-12
• Last Update Posted: 2018-12-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• Diagnosis of acute kidney injury as diagnosed by renal care team
• On medical or surgical services
• Over 18 year of age
• Ability to read and speak English

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Exclusion Criteria

• Legal blindness or deafness
• Pregnant
• Cognitive impairment that limits ability to consent

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
mHealth Tool	mHealth tool	* Complete a survey asking about kidney function and participant demographics. * Review a 15-20 minute educational tool on a tablet about kidney health * Receive a one-month follow-up call (one month after hospital discharge date) and complete a phone survey about patient kidney function after discharge

Primary Outcome Measures

Name	Time	Method
Change in Patient Safety-Related Knowledge (Patient safety risk awareness)	Baseline, 1 month	mHealth tool and how knowledge changes pre/post intervention
Change in Patient Safety Behavior and Risk awareness	Baseline, 1 month	Survey assessing patient safety behavior and risk awareness

Secondary Outcome Measures

Name	Time	Method
User Satisfaction	5 minutes	Satisfaction of mHealth tool

Trial Locations

Locations (1)

Duke University Hospital; 🇺🇸 Durham, North Carolina, United States