ClinicalTrials.Veeva

Menu

A Study of Facilitators and Barriers to Improve Acute Kidney Injury in Children Through Mobile Health Intervention

Duke University logo

Duke University

Status

Enrolling

Conditions

Acute Kidney Injury

Treatments

Other: mobile health educational tool

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04403633
Pro00104197
1R38HL143612-01 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to improve patient-centered care for acute kidney injury (AKI) in order to decrease the adverse health outcomes associated with this common condition.

Full description

There is a need to provide better patient-centered care for acute kidney injury (AKI) in order to improve the adverse health outcomes associated with this common condition. This project involves thorough evaluation of patient and provider feedback on barriers and facilitators to pediatric AKI self-management in order to develop patient-centered pediatric AKI interventions. This will be done through interviews with families of patients diagnosed with AKI and providers who take care of these patients followed by integration of the results into modification of an existing educational tool previously used in adult patients. The study will take place in three parts with the first involving interviews, the second involving tool modification and usability testing, and the third involving pilot testing of the tool's impact.

Enrollment

25 estimated patients

Sex

All

Ages

1 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • age 1 to 18 years
  • patients with diagnosis of AKI while hospitalized

Exclusion criteria

  • legal blindness of deafness
  • cognitive impairment that limits ability to consent
  • non-English speaking
  • patient age greater than age 18 years, 11 months

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

25 participants in 2 patient groups

Receiving Educational Tool
Experimental group
Description:
Patients in this arm will receive the educational tool after the pretest in addition to usual care.
Treatment:
Other: mobile health educational tool
Receiving Usual Care
No Intervention group
Description:
Patients in this arm will receive usual care after the pretest.

Trial contacts and locations

1

Loading...

Central trial contact

Anna Williams

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems